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  Pharmaceutical Patents  

 

Title:  PDE11A mutations in adrenal disease
United States Patent: 
7,847,078
Issued: 
December 7, 2010

Inventors:
 Stratakis; Constantine A. (Rockville, MD)
Assignee:
  The United States of America as represented by the Department of Health and Human Services (Washington, DC)
Appl. No.:
 12/161,866
Filed:
 January 19, 2007
PCT Filed:
 January 19, 2007
PCT No.:
 PCT/US2007/060746
371(c)(1),(2),(4) Date:
 August 26, 2008
PCT Pub. No.:
 WO2007/087493
PCT Pub. Date:
 August 02, 2007


 

Outsourcing Guide


Abstract

The invention provides previously uncharacterized variants of PDE11A that are correlated with a newly discovered form of Cushing Syndrome that presents at a young age. The invention also provides methods useful to research, screen for, treat, or prevent diagnose the disease using the PDE11A variants, as well as other methods relating thereto.

Description of the Invention

BRIEF SUMMARY OF THE INVENTION

The invention provides a method of screening for Cushing's syndrome or BAR in a mammal comprising (a) determining the activity or expression level of a PDE11A protein in a mammal, and (b) comparing the activity or expression level of the PDE11A protein in the mammal with a negative control, wherein decreased activity or expression of the PDE11A protein in the mammal as compared to the negative control is indicative of Cushing's syndrome or BAR. Similarly, the invention provides a method of screening for cancer or tumors in a mammal comprising (a) determining the activity or expression level of a PDE11A protein in a mammal, and (b) comparing the activity or expression level of the PDE11A protein in the mammal with a negative control, wherein decreased activity or expression of the PDE11A protein in the mammal as compared to the negative control is indicative of cancer or tumors in the mammal.

The invention provides a method of screening for Cushing's syndrome or BAH in a mammal comprising detecting a mutation in PDE11A of the mammal, wherein the presence of a mutation in PDE11A is indicative of Cushing's syndrome or BAH. Similarly, the invention provides a method of screening for cancer or tumors in a mammal comprising detecting a mutation in PDE11A of the mammal, wherein the presence of a mutation in PDE11A is indicative of cancer or tumors in a mammal.

The invention provides an isolated nucleic acid comprising one or more nucleic acid sequences selected from the group consisting of SEQ ID NOs: 1-5, as well a polypeptide encoded by the nucleic acid, and a vector and cell comprising the nucleic acid. Similarly, the invention provides an isolated nucleic acid sequence comprising SEQ ID NO: 25.

The invention provides a transgenic non-human mammal and a recombinant cell comprising a mutation of a nucleotide residue of PDE11A selected from the group consisting of (a) nucleotide residue 171 of Exon 3, (b) nucleotide residue 919 of Exon 4, (c) any one or more of nucleotide residues 1655-1657 of Exon 12, (d) nucleotide residue 2411 of Exon 19, and (e) any one or more of nucleotide residues 2758-2760 of Exon 23. Similarly, the invention provides a transgenic non-human mammal and a recombinant cell comprising a mutation of nucleotide residue 2599 of Exon 22 of PDE11A.

The invention provides a method of identifying an agent that modulates the activity of a polypeptide of the invention (e.g., a polypeptide encoded by a nucleic acid disclosed herein) comprising (a) contacting a cell that expresses the polypeptide with a test agent, and (b) comparing the activity or expression of the polypeptide in the presence of the test agent with the activity of the polypeptide in the absence of the test agent, wherein a difference in activity or expression of the polypeptide in the presence of the test agent as compared to the activity or expression of the polypeptide in the absence of the test agent is indicative that the test agent can modulate the activity of the polypeptide.

The invention provides a method of testing an agent for potential efficacy in treating Cushing's syndrome or BAH comprising (a) contacting a cell that expresses a PDE11A polypeptide with a test agent, and (b) comparing the activity or expression of the PDE11A polypeptide in the presence of the test agent with the activity or expression of the PDE11A polypeptide in the absence of the test agent, wherein a difference in the activity or expression of the PDE11A polypeptide in the presence of the test agent as compared to the activity or expression of the PDE11A polypeptide in the absence of the test agent is indicative of the test agent's potential efficacy against Cushing's syndrome or BAH.

The invention provides a method of testing an agent for potential efficacy in treating Cushing's syndrome or BAH comprising (a) administering a test agent to a transgenic non-human mammal of the invention, wherein the transgenic non-human mammal exhibits, prior to administration of the test agent, a phenotype selected from the group consisting of adrenal hyerplasia, endocrine cancer, non-endocrine cancer, malignant hypertension, immunosuppression, or any combination thereof, and (b) detecting a change in the phenotype of the transgenic non-human mammal subsequent to administration of the test agent, wherein amelioration of the phenotype subsequent to administration of the test agent is indicative of the test agent's potential effectiveness against Cushing's syndrome or BAH.

The invention provides a method of evaluating the safety of an inhibitor of PDE11A comprising (a) administering a PDE11A inhibitor to a mammal, (b) measuring subsequent to administration of the PDE11A inhibitor the level of cAMP or cGMP in a tissue of the mammal that normally expresses PDE11A, and (c) comparing the cAMP or CGMP level of the tissue with a negative control, wherein a change in the cAMP or cGMP level of the tissue as compared to the negative control is indicative that the inhibitor of PDE11A is unsafe for administration to humans.

The invention provides a method of evaluating the safety of an inhibitor of PDE11A comprising (a) administering the PDE11A inhibitor to a mammal, and (b) detecting subsequent to administration a histological change in a tissue of the mammal that normally expresses PDE11A, wherein a histological change in the tissue is indicative that the inhibitor of PDE11A is unsafe for administration to humans.

The invention also provides a method of evaluating the safety of an inhibitor of PDE11A comprising (a) administering the inhibitor of PDE11A to a mammal, and (b) detecting in the mammal subsequent to administration a symptom of Cushing's syndrome or BAH, wherein the presence of a symptom of Cushing's syndrome or BAH is indicative that the inhibitor of PDE11A is unsafe for administration to humans.

The invention further provides a nucleic acid probe comprising a nucleic acid sequence that binds to any of SEQ ID NOs: 1-5 or binds to a complementary sequence thereof, wherein the nucleic acid probe binds to any of SEQ ID NOs: 1-5 with greater affinity that to a non-mutant PDE11A sequence. Similarly, the invention provides a nucleic acid probe comprising a nucleic acid sequence that binds to SEQ ID NO: 25 or binds to a complementary sequence thereof, wherein the nucleic acid probe binds to SEQ ID NO: 25 with greater affinity that to a non-mutant PDE11A sequence.

Additionally, the invention provides a kit for detecting a mutation in PDE11A comprising one or more nucleic acids probes of the invention and any one or more of the following: (a) a reference nucleic acid sequence corresponding to the nucleic acid sequence of non-mutant PDE11A, its mRNA, or any relevant part thereof, (b) a reagent for detecting the nucleic acid, (c) a reagent for amplifying the nucleic acid, (d) instructions to use the nucleic acid to detect a mutation in PDE11A, (e) the location of a mutation of PDE11A, in electronic or other form, or (f) the nucleic acid sequence of any of SEQ ID NOs: 1-5 in electronic or other form. Similarly, the invention provides a kit for detecting a mutation in PDE11A comprising one or more nucleic acids probes of the invention and any one or more of the following: (a) a reference nucleic acid sequence corresponding to the nucleic acid sequence of non-mutant PDE11A, its mRNA, or any relevant part thereof, (b) a reagent for detecting the nucleic acid, (c) a reagent for amplifying the nucleic acid, (d) instructions to use the nucleic acid to detect a mutation in PDE11A, (e) the location of a mutation of PDE11A, in electronic or other form, or (f) the nucleic acid sequence of SEQ ID NO: 25 in electronic or other form.

The invention provides an array comprising one or more nucleic acid probes of the invention immobilized on a solid support.

DETAILED DESCRIPTION OF THE INVENTION

The phosphodiesterase 11A (PDE11A) locus, like that of other phosphodiesterases, has a complex genomic organization (Hetman et al., Proc. Nalt. Acad. Sci. U.S.A., 97:12891-12895 (2000); Fawcett et al., Proc. Natl. Acad. Sci. U.S.A., 97: 3702-3707 (2000); Yuasa et al., J. Biol. Chem., 275: 31469-31479 (2000); Yuasa et al., Eur. J. Biochem., 268: 4440-4448 (2001); and Yuasa et al., Eur. J. Biochem., 268: 168-178 (2001)). PDE11A catalyzes the hydrolysis of both cAMP and cGMP (Saenz de Tejada et al., Int. J. Impot. Res., 14(Suppl 4): S20 (2002); Gbekor et al., J. Urol., 167(Suppl): 246 (2002); Loughney et al., Int. J. Impot. Res., 17: 320-325 (2005); and D'Andrea et al. J. Histochem. Cytochem., 53: 895-903 (2005)). Four splice variants of PDE11A have been discovered: PDE11A1, PDE11A2, PDE11A3, and PDE11A4. Expression of PDE11A1] appears to be ubiquitous, whereas the PDE11A2 and PDE11A3 isoforms are expressed in testis. Only PDE11A4 is expressed in the adrenal cortex. The mRNA transcripts corresponding to the four splice variants of PDE11A are collectively referred to herein as the "PDE11A mRNA transcripts" and the proteins encoded by the transcripts are collectively referred to herein as the "PDE11A proteins."

The invention provides a method of screening for Cushing's syndrome (CS) or bilateral adrenal hyperplasia (BAH) in a mammal on the basis of the activity or expression level of a PDE11A protein, or mutations in the PDE11A gene. Without wishing to be bound by any particular theory, it is believed that CS and BAH, especially the childhood forms of CS and BAH, can be caused by a genetic defect in PDE11A, particularly with respect to the expression of the PDE11A4 splice variant. It is further believed that the genetic defect reduces the activity of PDE11A, especially PDE11A4 which comprises exons 3-6 and 8-23 of PDE11A, either by downregulation of expression or by expression of a protein with reduced functionality, resulting in increased cAMP and/or cGMP levels that lead to the symptoms of CS or BAH.

According to one aspect, the method of screening for CS or BAN in a mammal comprises (a) determining the activity or expression level of a PDE11A protein in the mammal, and (b) comparing the activity or expression level of a PDE11A protein in the mammal with a negative (i.e., normal) control, wherein decreased activity or expression of the PDE11A protein in the mammal as compared to the negative control is indicative of CS or BAH. The PDE11A protein is preferably PDE11A4

The term "screen" or "screening" as used herein means to test or examine. For instance, screening encompasses detecting the presence of a symptom or a disease, or the propensity to develop such a symptom or disease (e.g., a symptom of BAH, CS, cancer, tumors, etc.). Screening also encompasses testing or examining compounds for a physical property or physiological effect, or the probability that a compound will exhibit a physiological effect. A method of screening, as used herein, can be used to research, detect, diagnose, treat, or prevent a condition such as BAH, CS, cancer, tumors, etc., or to discover or develop a compound for research or clinical use (e.g., to determine the efficacy, toxicity, or appropriate dosage levels of a compound).

The mammal can be any mammal, including a cat, dog, horse, rabbit, goat, monkey, cow, pig, or rodent, such as a rat, guinea pig, or mouse. The mammal is preferably a human. The mammal can be symptomatic or asymptomatic for CS or BAH. The mammal can be suspected of having CS or BAH or at risk for such a condition, for example, a mammal presenting with micronodular BAH at an early age (e.g., a human presenting with micronodular BAH under the age of 10 years, or even under the age of 7 years or 5 years), or a mammal with a family history of BAH or CS (e.g., a mammal with a blood relation to another mammal diagnosed with micronodular BAH or CS presenting at an early age).

The activity or expression level of the PDE11A protein in the mammal can be determined by any suitable method. Typically, the activity or expression level of the protein in the mammal is determined by assaying the activity or expression level of the protein in a biological sample obtained from the mammal. The biological sample can be any suitable sample, such as a sample of body fluid (e.g., blood, blood plasma, blood serum, serous fluid, lymph fluid, saliva, urine, etc) or tissue (e.g., especially tissue from the adrenal gland, or from an adrenal tumor). The sample is preferably a sample of the adrenal gland of the mammal. The biological sample also can be any isolated or fractioned component of the foregoing (e.g., isolated DNA, RNA, or protein from a sample of body fluid or tissue).

The activity level of a PDE11A protein can be determined by assaying or measuring the affinity of the protein for its substrate, the kinetics of the reaction of the PDE11A protein with its substrate, or the rate or degree of catalysis of the substrate. For example, the activity level of a PDE11A protein can be determined by assaying or measuring the ability (i.e., catalytic efficiency) of the protein to hydrolyze cyclic adenosine 3',5'-monophosphate (cAMP) or cyclic guanosine 3',5'-monophosphate (cGMP). The enzyme activity of a PDE11A protein also can be determined indirectly by detecting abnormal cAMP or cGMP levels in a tissue that expresses the PDE11A protein. For example, deficient PDE11A4 activity will result in elevated cAMP or cGMP levels in tissues that normally express PDE11A4, such as the adrenal glands, prostate, or testes. Specific protocols for suitable assays are known in the art.

The expression level of a PDE11A protein can be determined on the basis of mRNA or protein quantification. Specific protocols for quantifying mRNA and protein levels are known in the art (e.g., microarray analysis and Western blot). Probes and antibodies useful for such procedures can be generated from the sequences provided herein using routine techniques, some of which are discussed in connection with other aspects of the invention.

The negative (i.e., normal) control can be any suitable control or standard that reflects the activity or expression level of the PDE11A protein of interest in a mammal that contains a non-mutant PDE11A gene. Typically, the negative control will be the activity or expression level of the PDE11A protein in an appropriate mammal with a non-mutant PDE11A, such as a mammal that does not have CS or BS or any other condition associated with a mutation in PDE11A. The control also can be provided by a compilation of activity or expression levels of the PDE11A protein from a pool of such individuals (e.g., a standardized activity or expression profile of the PDE11A protein of interest).

While any decrease in the activity or expression level of the PDE11A protein relative to the negative control can be indicative of CS or BAH, it is believed, without wishing to be bound by any particular theory, that the likelihood that CS or BAH is present increases with greater deviance from the negative control. Thus, while a positive result in the screen can be indicated by a decrease in PDE11A activity or expression relative to the negative control of any amount, preferably a positive result is indicated by a decrease of at least about 10% or more (e.g., at least about 15% or more, 20% or more, about 25% or more, about 30% or more, about 35% or more, about 40% or more, about 45% or more, about 50% or more, about 55% or more, about 60% or more, about 65% or more, about 70% or more, about 75% or more, about 80% or more, about 85% or more, about 90% or more, about 95% or more, or even about 100%).

In a related aspect, the method of screening for CS or BAH in a mammal comprises detecting in the mammal a mutation in PDE11A4 or the gene product of PDE11A, especially a mutation in PDE11A4 (e.g., the PDE11A4 mRNA or protein). The mammal can be any mammal as previously described, preferably a human.

A mutation in PDE11A or its gene product can be detected, for instance, by obtaining a sample from the mammal, which can be any sample as previously described that contains genetic material, and isolating and sequencing the PDE11A gene or gene product. The sequence of the PDE11A gene or gene product can then be compared to the sequence of a known normal (non-mutant) PDE11A gene or gene product, as appropriate. Normal, non-mutant PDE11A genes include any naturally occurring PDE11A gene that produces a fully-functional gene product in vivo at an expression level that is equivalent to the expression level in a normal control. A normal control is as previously defined herein.

By way of example, a normal non-mutant human PDE11A gene sequence is referenced by GenBank Accession No. ABO48423. The sequences of the mRNA and protein gene products of the PDE11A gene are referenced by GenBank Accession Nos. NM.sub.--016953 and NP.sub.--058649, respectively. The amino acid sequences of the isoforms of PDE11A include GenBank Accession Nos. BAB62714, BAB62713, and BAB52712. Nucleic acid probes suitable for isolating PDE11A or its mRNA transcripts can be designed from the nucleic acid sequences provided herein using routine techniques. Similarly, antibodies and antibody fragments suitable for isolating PDE11A proteins, especially PDE11A4, are commercially available or known in the art, or can be obtained using the polypeptides encoded by the nucleic acid sequences disclosed herein by routine techniques. Nucleic acid probes and antibodies are further discussed in connection with other aspects of the invention.

Any mutation in PDE11A or the gene product thereof (e.g., a mutation in an exon of PDE11A), especially PDE11A4, can be used as a basis for a positive result in the method of screening. Preferably, the gene mutation is a fully or partially inactivating mutation. As used herein, a mutation is fully or partially inactivating if it decreases or eliminates expression of the gene product, as determined by mRNA or protein levels, or causes the gene to express a protein that is partially or completely non-functional in any respect, preferably with respect to the ability to catalyze hydrolysis of cAMP or cGMP.

By way of illustration, several naturally occurring (i.e., non-engineered) mutations have been discovered in PDE11A that result in decreased expression levels or reduced activity levels of the PDE11A gene product, particularly PDE11A4. For example, SEQ ID NO: 1 sets forth the nucleic acid sequence of Exon 3 of a naturally occurring mutant PDE11A, wherein the thymine (T) residue normally occurring at nucleotide residue 171 of the non-mutant PDE11A has been deleted resulting in a premature stop codon (c.171delTfs41X). Similarly, SEQ ID NO: 2 provides the nucleic acid sequence of Exon 4 of a naturally occurring mutant PDE11A, wherein the cysteine (C) residue normally present at residue 919 of the non-mutant PDE11A has been substituted with a thymine (T) residue (c.919C>T/p.Arg307X) resulting in a premature stop codon. SEQ ID NO: 3 provides the nucleic acid sequence of Exon 12 of a naturally occurring mutant PDE11A, wherein the TCT residues normally present at positions 1655-1657 of the non-mutant PDE11A have been replaced with two cysteine residues (CC) resulting in a premature stop codon (c.1655-1657delTCT/insCCfs15X). SEQ ID NO: 4 provides the nucleic acid sequence of Exon 19 of a naturally occurring mutant PDE11A, wherein a guanine (G) residue normally present at position of 2411 of the non-mutant PDE11A has been substituted with adenine (A). The gene mutation translates into a substitution of arginine with histidine at amino acid residue 804 of the protein product, which is a highly conserved region of the protein (c.2411G>A/p.804Arg>His). SEQ ID NO: 5 provides the nucleic acid sequence of Exon 23 of a naturally occurring mutant PDE11A, wherein TCC residues normally present at positions 2758-2760 of the non-mutant PDE11A have been deleted, resulting in a deletion of a serine residue at position 920 of the protein product (c.2758-2760delTCC/p.Ser920del). SEQ ID NO: 25 provides the nucleic acid sequence of Exon 22 (and some surrounding intronic sequence) of a naturally occurring mutant PDE11A, wherein a cysteine (C) residue normally present at position 2599 of the non-mutant PDE11A has been substituted with guanine (G). The gene mutation translates into a substitution of arginine with glycine at amino acid residue 867 of the protein product, which is a highly conserved region of the protein (c.2599C>G/p.867Arg>Gly).

Thus, while the method of screening for CS or BAH can comprise detecting any mutation in PDE11A or its gene product, the method preferably comprises detecting one or more of the forgoing specific mutations or a different mutation in the region of PDE11A in which any of the foregoing specific mutations occur. In particular, the method preferably comprises detecting a mutation in an exon of PDE11A that is part of the PDE11A4 splice variant, preferably a mutation in one or more of Exons 3, 4, 12, 19, 22, or 23 of PDE11A. More particularly, the method can comprise detecting a mutation that comprises a substitution or deletion of a nucleotide residue of non-mutant human PDE11A selected from the group consisting of (a) nucleotide residue 171 of Exon 3, (b) nucleotide residue 919 of Exon 4, (c) any one or more of nucleotide residues 1655-1657 of Exon 12, (d) nucleotide residue 2411 of Exon 19, (e) any one or more of nucleotide residues 2758-2760 of Exon 23, and (f) nucleotide residue 2599 of Exon 22. For instance, the method can comprise detecting a nucleic acid sequence of any of SEQ ID NOs: 1-5 and 25 or a nucleic acid sequence that comprises about 85% or greater, (e.g., about 90% or greater, 95% or greater, or even about 99% or greater) sequence identity to any of SEQ ID NOs: 1-5 and 25. Methods for detecting specific mutations, such as the mutations described herein, using the nucleic acid sequences provided in SEQ ID NOs: 1-5 and 25 are known in the art and are further discussed in connection with other aspects of the invention.

In a related aspect, the invention provides an isolated nucleic acid comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 25 or a combination thereof, as well as a polypeptide encoded by the nucleic acid. Also encompassed by the invention is a nucleic acid comprising a degenerate nucleic acid sequence of any one of SEQ ID NOs: 1-5 and 25, which encode the same protein as encoded by any one of SEQ ID NOs: 1-5 and 25, or a nucleic acid sequence that is otherwise substantially identical to any one of SEQ ID NOs: 1-5 and 25. Substantially identical sequences include any sequence that has a sequence identity to any one of SEQ ID NOs: 1-5 and 25 of 85% or more, preferably 90% or more, or even 95% or more, as determined using available algorithms (e.g., the Basic Local Alignment Search Tool (BLAST) made publicly available through the National Center for Biotechnology Information, Bethesda, Md.). Similarly, the invention encompasses a polypeptide encoded by any of the foregoing nucleic acid sequences (e.g., SEQ ID NOs: 1-5 and 25 and sequences degenerate to or substantially identical to SEQ ID NOs: 1-5 and 25), which can further comprise one or more conservative amino acid substitutions, provided that such substitutions do not obliterate the function of the polypeptide. Preferably, the number of amino acid substitutions is not greater than 15% of the total number of amino acid residues, more preferably not greater than 10% or even 5% of the amino acid residues. As used herein, the term isolated means removed from its natural environment, synthetically generated, or otherwise engineered.

The nucleic acid can be provided as part of a vector (e.g., a vector comprising the nucleic acid). Any suitable vector can be used. Suitable vectors include nucleic acid vectors, such as naked DNA and plasmids, liposomes, molecular conjugates, and viral vectors, such as retroviral vectors, parvovirus-based vectors (e.g., adenoviral-based vectors and adeno-associated virus (AAV)-based vectors), lentiviral vectors (e.g., Herpes simplex (HSV)-based vectors), and hybrid or chimeric viral vectors, such as an adenoviral backbone with lentiviral components (see, ergs, Zheng et al., Nat. Biotech., 18(2): 176-80 (2000); International Patent Application WO 98/22143; International Patent Application WO 98/46778; and International Patent Application WO 00/17376) and an adenoviral backbone with AAV components (see, e.g., Fisher et al., Hum. Gene Ther., 7: 2079-2087 (1996)). Vectors and vector construction are known in the art (see, e.g., Sambrook et al., Molecular Cloning: A Laboratory Manual, 3.sup.rd Edition, Cold Spring Harbor Laboratory Press, New York (2001); and Ausubel et al., Current Protocols in Molecular Biology, Green Publishing Associates and John Wiley & Sons, New York, N.Y. (1994)).

The vector can comprise any suitable promoter and other regulatory sequences (e.g., transcription and translation initiation and termination codons) to control the expression of the nucleic acid sequence. The promoter can be a native or nonnative promoter operably linked to the nucleic acid described above. The selection of promoters, including various constitutive and regulatable promoters, is within the skill of an ordinary artisan. Examples of regulatable promoters include inducible, repressible, and tissue-specific promoters. Specific examples include viral promoters, such as adenoviral promoters, AAV promoters, and CMV promoters. Additionally, operably linking the nucleic acid described above to a promoter is within the skill in the art.

The nucleic acid or vector can be introduced into a cell, thereby providing a recombinant cell comprising the nucleic acid, optionally in a vector. Any suitable cell (e.g., an isolated cell) can be used. Examples include host cells, such as E. coli (e.g., E. coli Tb-1, TG-2, DH5.alpha., XL-Blue MRF' (Stratagene), SA2821, and Y1090), Bacillus subtilis, Salmonella typhimurium, Serratia marcescens, Pseudomonas (e.g., P. aerugenosa), N. grassa, insect cells (e.g., Sf9, Ea4), yeast (S. cerevisiae) cells, and cells derived from a mammal, including human cell lines. Specific examples of suitable eukaryotic cells include VERO, HeLa, 3T3, Chinese hamster ovary (CHO) cells, W138 BHK, COS-7, and MDCK cells. Methods of introducing vectors into isolated host cells and the culture and selection of transformed host cells in vitro are known in the art and include the use of calcium chloride-mediated transformation, transduction, conjugation, triparental mating, DEAE, dextran-mediated transfection, infection, membrane fusion with liposomes, high velocity bombardment with DNA-coated microprojectiles, direct microinjection into single cells, and electroporation (see, e.g., Sambrook et al., supra, Davis et al., Basic Methods in Molecular Biology (1986), and Neumann et al., EMBO J. 1: 841 (1982)). Preferably, the recombinant cell expresses the polypeptide encoded by the nucleic acid of the invention.

The recombinant cell can be an isolated cell, a cell of a cell culture, a cell of a tissue, or a cell of a host, such as a mammal or human. In this regard, the invention also provides a transgenic non-human mammal or recombinant cell that comprises a mutation in one or more exons of PDE11A selected from the group consisting of Exon 3, Exon 4, Exon 12, Exon 19, Exon 22, and Exon 23. Preferably, the mutation is an inactivating mutation, such as any one or more of the specific mutations described herein with respect to the method of screening. More particularly, the transgenic non-human mammal or recombinant cell can comprise a nucleic acid having the sequence of any of SEQ ID NOs: 1-5 and 25, optionally in the form of a vector. The transgenic non-human mammal or recombinant cell can be any suitable mammal or cell, as previously described. Preferably, the transgenic non-human mammal is a mouse or other rodent. The transgenic non-human mammal desirably exhibits adrenal hyperplasia, endocrine cancer and/or other tumor conditions, non-endocrine cancer and/or other tumor conditions, malignant hypertension, or any combination thereof.

Transgenic non-human mammals can be prepared by routine methods known in the art. The term "transgenic" is intended to encompass genetically modified mammals having a deletion or other knock-out of an endogenous gene, having an exogenous gene (e.g. a nucleic acid comprising one or more nucleic acid sequences selected from the group consisting of SEQ ID NOs: 1-5 and 25) that is stably transmitted in the host cells, and/or having an exogenous promoter operably linked to a reporter gene (e.g., lacZ). Transgenic mammals can be made through homologous recombination, where the allele locus is altered. The exogenous gene is usually from a different species than the mammal host. Where the exogenous gene is a coding sequence, it usually is operably linked to a promoter, which may be constitutive or inducible, and other regulatory sequences required for expression in the host animal. Alternatively, a nucleic acid construct is randomly integrated into the genome. Vectors for stable integration include plasmids, retroviruses and other animal viruses, YACs, and the like.

DNA constructs for homologous recombination can comprise at least a portion of the mutant of the PDE11A gene with the desired genetic modification, and can include regions of homology to the target locus. DNA constructs for random integration need not include regions of homology to mediate recombination. For various techniques for transfecting mammalian cells, see Keown et al., Methods in Enzymology, 185: 527-537 (1990).

The modified cells or mammals can be used for any purpose. For example, the modified cells or mammals can be used for research in order to study of the physiological effect of the PDE11A mutants or in functional studies, such as drug screening, for example, to determine the effect of a candidate drug. Transgenic cells and mammals are also useful as part of a pre-clinical program.

In this respect, the invention provides a method of identifying an agent that modulates the activity or expression of a polypeptide encoded by the nucleic acid described herein, which method comprises (a) contacting a cell that expresses the polypeptide with a test agent, and (b) comparing the activity or expression of the polypeptide in the presence of the test agent with the activity or expression of the polypeptide in the absence of the test agent, wherein a difference in activity or expression is indicative that the test agent modulates the activity or expression of the polypeptide.

The term "modulate" refers to any change or alteration in the activity or expression of any of the isoforms of PDE11A (especially the PDE11A4 isoform). Modulation may be an increase or a decrease in protein activity, a change in binding characteristics, or any other change in the biological or functional properties of any of the isoforms of PDE11A. Modulation also includes an increase or decrease in the expression of any of the PDE11A isoforms to any degree. The difference in PDE11A activity or expression that is indicative that the test agent modulates PDE11A activity or expression can be a difference of any amount, but is preferably a difference of at least about 10% or greater (e.g., about 15% or greater, about 20% or greater, about 25% or greater, about 30% or greater, about 35% or greater, about 40% or greater, about 45% or greater, about 50% or greater, about 55% or greater, about 60% or greater, about 65% or greater, about 70% or greater, about 75% or greater, about 80% or greater, about 85% or greater, about 90% or greater, about 95% or greater or about 100%). The test agent preferably increases PDE11A activity or expression.

All other aspects of the method of identifying an agent that modifies the activity of the polypeptide encoded by a nucleic acid of the invention is as described herein with respect to the other aspects of the invention.

Additionally, the invention provides a method of testing an agent for potential efficacy in treating CS or DAM. In a first aspect, the method comprises (a) administering a test agent to the transgenic non-human mammal, as described herein, wherein the transgenic non-human mammal, prior to administration of the test agent, exhibits a phenotype selected from the group consisting of adrenal hyperplasia, endocrine cancer, non-endocrine cancer, malignant hypertension, immunosuppression, or any combination thereof, and (b) detecting a change in the phenotype of the transgenic non-human mammal subsequent to administration of the test agent, wherein amelioration of the phenotype is indicative of the agent's potential effectiveness against CS or BAH. As used herein, amelioration of a phenotype or condition means a lessening of the severity of the symptoms of the phenotype or condition to any degree, such as a decrease in cancer mass, a decrease in blood pressure, etc.

In another aspect, the method of testing an agent for potential efficacy in treating CS or BAH comprises (a) contacting a cell that expresses a PDE11A polypeptide with a test agent, and (b) comparing the activity or expression of the PDE11A polypeptide in the presence of the test agent with the activity or expression of the PDE11A polypeptide in the absence of the test agent, wherein a difference in the activity or expression of the PDE11A polypeptide in the presence of the test agent as compared to the activity or expression of the PDE11A polypeptide in the absence of the test agent is indicative of the test agent's potential efficacy against CS or BAH. Preferably, the PDE11A polypeptide is PDE11A4.

All other aspects of the method of testing an agent for potential efficacy in treating CS or BAH are as described herein with respect to the other aspects of the invention.

Agents that modulate the activity or expression of a PDE11A polypeptide, such as a polypeptide encoded by a nucleic acid as described herein, or an agent that exhibits efficacy in treating CS or BAH, are useful for many purposes, such as for the research, prevention, or treatment of CS or BAH. Thus, the invention further provides a method of treating or preventing CS or BAH in a mammal, comprising administering to the mammal an agent that modulates the activity or expression of a PDE11A polypeptide, especially PDE11A4 or a polypeptide encoded by a nucleic acid described herein, whereupon CS or BAH is treated or prevented. The mammal can be any mammal as defined herein with respect to other aspects of the invention. The agent can be any suitable agent that modulates the activity or expression of PDE11A, such as an agent identified using the methods described above. The agent preferably increases PDE11A activity and can include, for instance, a nucleic acid that encodes a functional PDE11A protein, especially PDE11A4. The nucleic acid can be in the form of a vector. Suitable vectors and other components of a nucleic acid construct that could be used in this capacity are as described herein with respect to other aspects of the invention or as otherwise known in the art.

One skilled in the art will appreciate that various routes of administering the agent are available, and, although more than one route can be used for administration, a particular route can provide a more immediate and more effective reaction than another route. Suitable routes of administration of the agent can include parenteral, oral, rectal, and inhaled administration. It may also be suitable to administer the agent directly to the actual tissues, for instance, when the agent includes a nucleic acid that encodes a functional PDE11A protein, optionally in the form of a vector. Accordingly, there are a wide variety of suitable formulations of compositions that can be used in the inventive methods.

The agent described above, alone or in further combination with one or more other active agents, preferably is made into a formulation suitable for parenteral administration, and most preferably intraperitoneal administration. Such a formulation can include aqueous and nonaqueous, isotonic sterile injection solutions, which can contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood of the intended recipient, and aqueous and nonaqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. The formulations can be presented in unit dose or multi-dose sealed containers, such as ampules and vials, and can be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, water, for injections, immediately prior to use. Extemporaneously injectable solutions and suspensions can be prepared from sterile powders, granules, and tablets, as described herein.

The dose administered to a patient, such as a mammal, particularly a human, in the context of the present invention should be sufficient to effect a prophylactic or therapeutic response as desired in the mammal over a reasonable time frame. The dose will be determined by the potency of the agent as described above, the severity of a condition being treated, as well as the body weight and age of the patient. The size of the dose also will be determined by the existence of any adverse side effects that may accompany the use of the particular agent. It is always desirable, whenever possible, to keep adverse side effects to a minimum.

The dosage can be in unit dosage form, such as a tablet or capsule. The term "unit dosage form" as used herein refers to physically discrete units suitable as unitary dosages for human and mammalian subjects, each unit containing a predetermined quantity of an agent, alone or in combination with other active agents, such as anticancer agents, calculated in an amount sufficient to produce the desired effect in association with a pharmaceutically acceptable diluent, carrier, or vehicle. The specifications for the unit dosage forms of the invention depend on the particular embodiment employed and the effect to be achieved, as well as the pharmacodynamics associated with each agent in the patient. Other aspects of the method of treating or preventing CS or BAH are as described with respect to the other aspects of the invention.

One skilled in the art can easily determine the appropriate dose, schedule, and method of administration for the exact formulation of the composition being used, in order to achieve the desired effective amount in the individual patient. One skilled in the art also can readily determine and use an appropriate indicator of the effective amount of the agent of the invention by a direct or indirect analysis of appropriate patient samples (e.g., blood and/or tissues).

The invention also provides methods to evaluate the safety of an inhibitor of PDE11A, especially an inhibitor of PDE11A4. The term "inhibitor of PDE11A" or "PDE11A inhibitor" as used herein (with respect to all aspects of the invention) refers to any compound that reduces the activity or expression of PDE11A or an isoform thereof, especially PDE11A4, by any degree. Thus, a PDE11A inhibitor can reduce the activity or expression of PDE11A or an isoform thereof by 5% or more, 10% or more, 25% or more, 35% or more, 50% or more, 75% or more, or even 90% or 95% or more. A compound is considered a "PDE11A inhibitor" regardless of whether PDE11A is the primary target of the compound. Thus, for example, a compound that primarily inhibits a different member of the PDE family, but also inhibits an isoform of PDE11A to any degree, is a PDE11A inhibitor for the purposes of this invention. Examples of agents that inhibit or partially inhibit PDE11A include tadalafil (Clalis.RTM.) and sildenafil (Viagra.RTM.), which medications are widely used for the treatment of erectile dysfunction.

The safety of an inhibitor of PDE11A can be determined on the basis of the physiological effects of PDE11A inhibition, as described herein. For example, the safety of an inhibitor of PDE11A can be evaluated by a method comprising (a) administering a PDE11A inhibitor to a mammal, (b) measuring subsequent to administration of the PDE11A inhibitor the level of cAMP or cGMP in a tissue of the mammal that normally expresses PDE11A, and (c) comparing the cAMP or cGMP level of the tissue with a negative control, wherein a change in the cAMP or cGMP level of the tissue as compared to the negative control is indicative that the inhibitor of PDE11A is unsafe for administration to humans. In a related aspect, the method of evaluating the safety of an inhibitor of PDE11A can comprise (a) administering the PDE11A inhibitor to a mammal, and (b) detecting subsequent to administration a histological change in a tissue of the mammal that normally expresses PDE11A, wherein a histological change in the tissue is indicative that the inhibitor of PDE11A is unsafe for administration to humans.

Tissues that "normally" express PDE11A are defined herein as the tissues of a mammal that, in the absence of a PDE11A inhibitor, express an isoform of PDE11A. Such tissues include, for example, tissues of the adrenal gland, testes, or prostate gland. The cAMP and cGMP levels of such tissues can be determined by methods known in the art. In this regard, the "negative control" can be as described herein with respect to other aspects of the invention, and can be provided, for example, by the cAMP or eGMP level of the tested tissue in the absence of the PDE11A inhibitor (e.g., the cAMP or cGMP level of the tissue of the same test mammal prior to administration of the PDE11A inhibitor, or a mammal of the same type as the test mammal without administration of the PDE11A inhibitor). Also, the negative control can be provided by a standard profile developed from the CAMP or cGMP levels of relevant tissues from a group of such mammals.

Any change in the cAMP or cGMP level can be indicative of an unsafe compound, such as a change of about 5% or more, 10% or more, 25% or more, 35% or more, 50% or more, 75% or more, or even 90% or 95% or more. It is believed that an increase in the cAMP and/or cGMP level is indicative of a tendency to promote CS, BAH, or tumor formation in the relevant tissue.

Histological changes can be detected by histological examination techniques that are routine in the art. By "histological change" is meant a difference in the histology of the tissue subsequent to administration as compared to the histology of the tissue prior to administration. Histological changes can be inferred from a comparison of tissues of a mammal subsequent to administration to the tissues of the same type of mammal that did not undergo administration of the PDE11A inhibitor. Histological changes include tumor formation or any other change to the cells of the tissue that indicate an abnormality, especially changes to the cells that indicate cell proliferation, malignancy, or other abnormal tendency towards growth, cancer, or tumor formation.

In a related aspect, the safety of a PDE11A inhibitor can be evaluated by a method comprising (a) administering the inhibitor of PDE11A to a mammal, and (b) detecting in the mammal subsequent to administration a symptom of Cushing's syndrome or BAH, wherein the presence of a symptom of Cushing's syndrome or BAH is indicative that the inhibitor of PDE11A is unsafe for administration to humans. Any symptom of Cushing's syndrome or BAH can be used as a basis for the evaluation, including, for example, adrenal hyperplasia, endocrine cancer, non-endocrine cancer, malignant hypertension, immunosuppression, or any combination thereof. The symptoms of Cushing's syndrome or BAR can be detected using routine techniques.

Other aspects of the method of evaluating the safety of a PDE11A inhibitor are as described with respect to the other methods and compositions of the invention.

The invention further provides isolated nucleic acids that can be used as probes or primers for detecting mutations in PDE11A, as well as kits comprising such nucleic acids and methods of using the same.

An isolated nucleic acid useful as a probe or primer comprises a nucleic acid sequence that binds to any of SEQ ID NOs. 1-5 and 25 or binds to a complementary sequence thereof, preferably under high stringency conditions (e.g. a fragment of any of SEQ ID NOs: 1-5 and 25 or complementary sequence thereof). High stringency conditions, within the meaning of the present invention are conditions that allow for mismatch of four base pairs or less, preferably three base pairs or less, two base pairs or less, or even one base pair or no mismatch. Specific conditions meeting the above requirements are known in the art or can be determined by routine techniques. High stringency conditions include, for example, low salt and/or high temperature conditions, such as provided by about 0.02-0.1 M NaCl or the equivalent, at temperatures of about 50-70.degree. C.

Nucleic acids useful as probes should bind to any of SEQ ID NOs: 1-5 and 25 with a greater affinity than to a non-mutant PDE11A sequence, under appropriate conditions (e.g., high stringency conditions), thereby allowing the use of the probe to distinguish between the mutant and non-mutant sequences. Generally, such a probe can be designed by including the site of mutation in the probe itself. Thus, an isolated nucleic acid useful as a probe preferably comprises about 5 or more (e.g., about 7 or more, 10 or more, 15 or more, 20 or more, or even 30 or more) contiguous nucleotides of any of SEQ ID NOs: 1-5 and 25 or a nucleic acid sequence that is complementary to any of SEQ ID NOs: 1-5 and 25, wherein the isolated nucleic acid comprises the region of the sequence corresponding to the PDE11A mutation. For example, since SEQ ID NO: 1 provides the sequence of a mutant PDE11A Exon 3 comprising a deletion mutation of nucleotide residue 171, an isolated nucleic acid probe based on SEQ ID NO: 1 should include nucleotide residues 206-207 of SEQ ID NO: 1 or the appropriate nucleotides of a complementary sequence that corresponds to the mutation. The same is true with respect to SEQ ID NOs: 2-5 and 25, the corresponding PDE11A mutations of which have been described elsewhere herein. Thus, a nucleic acid probe based on SEQ ID NO: 2 should comprise the nucleotide at position 60 of SEQ ID NO: 2 or the appropriate position of a complementary sequence, which corresponds to a substitution mutation of nucleotide residue 919 of Exon 4 of PDE11A. Also, a nucleotide probe based on SEQ ID NO: 3 should comprise a nucleotide at one or more of positions 276-277 of SEQ ID NO: 3 or the appropriate position of a complementary sequence, thereby reflecting the TCT deletion that corresponds to nucleotide residues 1655-1657 of Exon 12 of PDE11A. Similarly, a nucleic acid probe based on SEQ ID NO: 4 should comprise the nucleotide at position 26 of SEQ ID NO: 4 or the appropriate position of a complementary sequence, which corresponds to a substitution mutation of nucleotide residue 2411 of Exon 19 of PDE11A. As well, a nucleotide probe based on SEQ ID NO: 5 should comprise nucleotides 209-213 of SEQ ID NO: 5, thereby reflecting a deletion of TCT at nucleotide residues 2758-2760 of Exon 23 of PDE11A. A nucleic acid probe based on SEQ ID NO: 25 should comprise the nucleotide at position 217 of SEQ ID NO: 25 or the appropriate position of a complementary sequence, which corresponds to a substitution mutation of nucleotide residue 2599 of Exon 19 of PDE11A. The probe can include one or more nucleic acid analogs, labels (e.g., a radioactive or fluorescent label), or other substituents or moieties as appropriate, provided that the base-pairing function is retained.

When the isolated nucleic acid is to be used as a primer, the nucleic acid preferably binds to PDE11A at a position flanking the site of mutation. Thus, the nucleic acid preferably comprises about 5 or more (e.g., about 7 or more, 10 or more, 15 or more, 20 or more, or even 30 or more) contiguous nucleotides of any of SEQ ID NOs: 1-5 and 25 or a nucleic acid sequence that is complementary to any of SEQ ID NOs: 1-5 and 25, wherein the nucleic acid binds to PDE11A or any of SEQ ID NOs: 1-5 and 25 at a position flanking a prospective mutation site selected from the group consisting of (i) nucleotide 171 of Exon 3, (ii) nucleotide 919 of Exon 4, (iii) nucleotides 1655-1657 of Exon 12, (iv) nucleotide 2411 of Exon 19, (v) nucleotides 2758-2760 of Exon 23, or (vi) nucleotide 2599 of Exon 22. By a position "flanking" a prospective mutation site is meant a position one or more nucleotides 5' or 3' from the prospective mutation site (e.g., 3 or more, 5 or more, or 10 or more nucleotides from the prospective mutation site, or even further from the prospective mutation site). Thus, the nucleic acid useful as a primer preferably does not comprise the prospective mutation site itself.

Specific examples of primers include nucleic acids comprising a sequence selected from the group consisting of SEQ ID NOs: 6-15. For instance, primers comprising SEQ ID NOs: 6 and/or 7 can be used to amplify a nucleic acid comprising the nucleic acid sequence of SEQ ID NO: 5; primers comprising SEQ ID NOs: 8 and/or 9 can be used to amplify a nucleic acid comprising the nucleic acid sequence of SEQ ID NO: 1; primers comprising SEQ ID NOs: 10 and/or 11 can be used to amplify a nucleic acid comprising the nucleic acid sequence consisting of SEQ ID NO: 2; primers comprising SEQ ID NOs: 12 and/or 13 can be used to amplify a nucleic acid comprising the nucleic acid sequence of SEQ ID NO: 3; and primers comprising SEQ ID NOs: 14 and/or 15 can be used to amplify a nucleic acid comprising the nucleic acid sequence of SEQ ID NO: 4.

The probes and primers can be used for any purpose, but are especially useful for detecting the PDE11A mutations described herein, which are believed to be the underlying causes of a childhood form of CS and BAH. There are many different methods of using the above described probes or primers to detect such mutations. By way of example, a method of detecting a mutation in PDE11A could comprise (a) contacting a biological sample with a polynucleotide probe, as described above, and (b) detecting a hybridization complex of the polynucleotide probe with a nucleic acid, wherein the detection of a hybridization complex indicates the presence of a mutation in PDE11A4. Alternatively, the method of detecting a mutation in PDE11A can comprise (a) contacting a biological sample with a primer as described above, (b) extending the primer to generate a copy of the nucleic acid sequence that includes the prospective mutation site, and (c) detecting a difference between the sequence of the copy and the sequence of a reference non-mutant PDE11A gene. A myriad of different techniques for detecting hybridization complexes and detecting differences between two nucleic acid sequences are known in the art, any of which can be used in conjunction with the invention. Also, conditions for the hybridization of probes and primers to the target and test sequences in the context of detecting single-nucleotide polymorphisms and disease-causing point mutations are described in the art, along with specific protocols for conducting such assays that are useful in conjunction with the invention. Furthermore, many methods of designing and using probes and primers, other than those described herein, to detect nucleic acid mutations are known (see, for example, Saiki et al., Nature, 324: 163-166 (1986); EP 235726; and WO 89/11548), and the description of the above specific examples is not intended to be limiting.

In a related aspect, a kit for detecting a mutation in PDE11A is provided herein comprising one or more nucleic acids that bind to one or more nucleic acid sequences of SEQ ID NOs: 1-5 and 25 (e.g., a probe or primer as described herein) and any one or more of the following: (a) a reference nucleic acid sequence corresponding to nucleic acid sequence of non-mutant PDE11A, its mRNA, or any relevant part thereof, (b) a reagent for detecting the nucleic acid, (c) a reagent for amplifying the nucleic acid, (d) instructions to use the nucleic acid to detect a mutation in PDE11A, (e) the location of a mutation of PDE11A, in electronic or other form, or (f) the nucleic acid sequence of any of SEQ ID NOs: 1-5 and 25 in electronic or other form.

Also provided herein is an array comprising one or more probes, as described herein, immobilized on a solid support. For convenience in analyzing the results, the array preferably comprises fewer than 100 different types of probes, preferably fewer than 50 different types of probes, or even fewer than 25 different types of probes (e.g., fewer than 15 or even 10 or 5 different types of probes). Methods for constructing arrays, as well as other aspects and features of suitable arrays are generally known in the art, specific examples of which are described by WO 95/11995. Arrays may be provided in the form of a multiplex chip. The array also can be part of the kit of the invention.

Other aspects of the probes, primers, kits, and arrays are as described with respect to other aspects of the invention.

The invention farther provides an antibody, or an antigen binding portion thereof, that binds to a polypeptide encoded by the nucleic acids described herein. The antibody can be any type of immunoglobulin that is known in the art. For instance, the antibody can be of any isotype, e.g., IgA, IgD, IgE, IgG, IgM, etc. The antibody can be monoclonal or polyclonal. The antibody can be a naturally-occurring antibody, e.g., an antibody isolated and/or purified from a mammal, e.g., mouse, rabbit, goat, horse, hamster, human, etc. Alternatively, the antibody can be a genetically-engineered antibody, e.g., a humanized antibody or a chimeric antibody. The antibody can be in monomeric or polymeric form. Also, the antibody can have any level of affinity or avidity for the polypeptides of the invention. Desirably, the antibody is specific for the polypeptide, such that there is minimal cross-reaction with other peptides or proteins, such as wild-type PDE11A4 protein.

Methods of testing antibodies for the ability to bind to the polypeptides are known in the art and include any antibody-antigen binding assay, such as, for example, radioimmunoassay (RIA), ELISA, Western blot, immunoprecipitation, and competitive inhibition assays (see, e.g., Janeway et al., Immunobiology: The Immune System in Health and Disease, 4.sup.th ed., Current Biology Publications: Garland Publishing, New York, N.Y., 1999)).

Suitable methods of making antibodies are known in the art. For instance, standard hybridoma methods are described in, e.g., Kohler and Milstein, Eur. J. Immunol., 5: 511-519 (1976), Harlow and Lane (eds.), Antibodies: A Laboratory Manual, CSSH Press (1988), and C. A. Janeway et al. (eds.), Immunobiology, 5.sup.th Ed., Garland Publishing, New York, N.Y. (2001)). Alternatively, other methods, such as EBV-hybridoma methods (Haskard and Archer, J. Immunol. Methods, 74(2): 361-67 (1984), and Roder et al., Methods Enzymol., 121: 140-67 (1986)), and bacteriophage vector expression systems (see, e.g., Huse et al., Science, 246, 1275-81 (1989)) are known in the art. Furthermore, methods of producing antibodies in non-human animals are described in, e.g., U.S. Pat. Nos. 5,545,806, 5,569,825, and 5,714,352.

Phage display also can be used to generate the antibody of the invention. In this regard, phage libraries encoding antigen-binding variable (V) domains of antibodies can be generated using standard molecular biology and recombinant DNA techniques (see, e.g., Sambrook et al., supra). Phage encoding a variable region with the desired specificity are selected for specific binding to the desired antigen, and a complete or partial antibody is reconstituted comprising the selected variable domain. Nucleic acid sequences encoding the reconstituted antibody are introduced into a suitable cell line, such as a myeloma cell used for hybridoma production, such that antibodies having the characteristics of monoclonal antibodies are secreted by the cell (see, e.g., Janeway et al., supra, Huse et al., supra, and U.S. Pat. No. 6,265,150).

Methods for generating humanized antibodies are well known in the art and are described in detail in, for example, Janeway et al., supra, U.S. Pat. Nos. 5,225,539, 5,585,089 and 5,693,761, European Patent No. 0239400 B1, and United Kingdom Patent No. 2188638. Humanized antibodies can also be generated using the antibody resurfacing technology described in U.S. Pat. No. 5,639,641 and Pedersen et al., J. Mol. Biol., 235: 959-973 (1994).

The invention also provides antigen binding portions of any of the antibodies described herein. The antigen binding portion can be any portion that has at least one antigen binding site, such as Fab, F(ab').sub.2, dsFv, scFv, diabodies, and triabodies.

A single chain variable region fragment (scFv) antibody fragment, which consists of a truncated Fab fragment comprising the variable (V) domain of an antibody heavy chain linked to a V domain of a light antibody chain via a synthetic peptide, can be generated using routine recombinant DNA technology techniques (see, e.g., Janeway et al., supra). Similarly, disulfide-stabilized variable region fragments (dsFv) can be prepared by recombinant DNA technology (see, e.g., Reiter et al., Protein Engineering, 7: 697-704 (1994)).

The antibodies can be used, for instance, to detect a mutant PDE11A protein (e.g., a mutant PDE11A4 protein). For example, such a method can comprise (a) contacting a biological sample with an antibody that binds to a polypeptide encoded by a nucleic acid described herein, but does not bind to a polypeptide comprising SEQ ID NO: 16 (the amino acid sequence of wild-type PDE11A protein), and (b) detecting the binding of the antibody to a polypeptide, wherein detection of the binding of the antibody to a polypeptide is indicative of the presence of the polypeptide. The detection of the binding of the antibody to the polypeptide can be done by any suitable method, such as Western blotting, immunoassays, and immunohistochemistry techniques known in the art.

Other aspects of the antibodies and method of detecting a mutant PDE11A protein are as described with respect to other aspects of the invention.

Although the foregoing has been described in reference to Cushing's syndrome and BAH, one of ordinary skill in the art will understand that the methods to research, screen for, treat, or prevent discussed herein can be used for diseases and disorders other than Cushing's syndrome or BAM that are associated with reduced activity or expression levels of PDE11A, especially PDE11A4, including tumor formation and cancer in tissues that express PDE11A, especially PDE11A4, such as the tissues of the prostate, adrenal glands, and testis.

Thus, the invention also provides method of screening for cancer or tumors in a mammal, especially with respect to a cancer or tumors of a tissue that expresses PDE11A, comprising (a) determining the activity or expression level of a PDE11A protein in a mammal, and (b) comparing the activity or expression level of the PDE11A protein in the mammal with a negative control, wherein decreased activity or expression of the PDE11A protein in the mammal as compared to the negative control is indicative of cancer or tumors in the mammal. In a related aspect, the method of screening for cancer or tumors in a mammal comprises detecting a mutation in PDE11A of the mammal, wherein the presence of a mutation in PDE11A is indicative of cancer or tumors in a mammal. All other aspects of the method of screening for cancer or tumors in a mammal are as described with respect to the other methods and compositions of the invention.
 

Claim 1 of 4 Claims

1. An isolated nucleic acid comprising SEQ ID NO: 3.

 

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