Since the development of the birth control pill for women, the past several decades have seen few advances in contraception. Furthermore, there is still no effective oral contraceptive pill for men. As stated in Healthy People 2010, """"""""contraceptive research and development efforts must be expanded to bring new methods to the market."""""""" Thus, we need more effective, inexpensive, long-acting, and easily administered contraceptives, especially for men. In this proposal, we will focus on four intriguing and evolutionarily-conserved proteins that we hypothesize are outstanding targets for novel contraceptives. Knockout studies have demonstrated that mice lacking GASZ, VASA, TEX14, and STYX have a block at different points in spermatogenesis ranging from spermatocytes to spermatids, resulting in sterility. With the aid of our collaborators, Drs. Angela Koehler, Peter Davies, and Laising Yen, the overall goal of this research proposal from the Matzuk laboratory is to identify small molecules and chemical analogs that bind to these spermatogenic-specific proteins to block their function and/or disrupt protein:protein complexes, thereby causing a contraceptive effect. Our overall hypothesis is that we will rapidly identify multiple lead compounds that are directed at these unique and essential spermatogenic proteins and can be used to synthesize an assortment of oral and implantable contraceptives for men.
The Specific Aims of these proposed U01 studies are: 1) Use small molecule microarrays and 2-hybrid screening assays to identify small molecules that bind GASZ, VASA, TEX14, or STYX and/or block key protein:protein interactions;and 2) Perform in vitro, in vivo, and computational screens to identify the most promising male contraceptives. Our studies are the first of their kind to use small molecule microarrays and mammalian 2-hybrid screening assays to identify small molecules that can act as contraceptives. We have put together a strong multidisciplinary group of scientists to tackle this important public health problem, and as a result, we believe that we can generate several novel contraceptives that will target unique proteins, structures, and processes in the germline in men.

Public Health Relevance

Despite the rapid increase in the world's population, the high rate of unintended pregnancies in U.S. teenagers (1 million per year), and the staggering cost to the American taxpayer of these unintended pregnancies ($7-$15 billion per year), there is no oral contraceptive for men. This application will focus on the identification of small molecules that target the male germline. Our studies are unique since they will use small molecule microarrays and protein:protein interaction assays to identify and characterize drugs that cause their contraceptive effect by inhibiting specific structures or pathways during spermatogenesis.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01HD060496-01
Application #
7626130
Study Section
Special Emphasis Panel (ZHD1-DSR-L (08))
Program Officer
Blithe, Diana
Project Start
2009-02-15
Project End
2014-01-31
Budget Start
2009-02-15
Budget End
2010-01-31
Support Year
1
Fiscal Year
2009
Total Cost
$248,670
Indirect Cost
Name
Baylor College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Miyata, Haruhiko; Castaneda, Julio M; Fujihara, Yoshitaka et al. (2016) Genome engineering uncovers 54 evolutionarily conserved and testis-enriched genes that are not required for male fertility in mice. Proc Natl Acad Sci U S A 113:7704-10
Wang, Qian; Liu, Xiqiang; Tang, Nannan et al. (2013) GASZ promotes germ cell derivation from embryonic stem cells. Stem Cell Res 11:845-60
Lim, Ai Khim; Lorthongpanich, Chanchao; Chew, Ting Gang et al. (2013) The nuage mediates retrotransposon silencing in mouse primordial ovarian follicles. Development 140:3819-25
Matzuk, Martin M; Burns, Kathleen H (2012) Genetics of mammalian reproduction: modeling the end of the germline. Annu Rev Physiol 74:503-28
Matzuk, Martin M; McKeown, Michael R; Filippakopoulos, Panagis et al. (2012) Small-molecule inhibition of BRDT for male contraception. Cell 150:673-84
Iwamori, Tokuko; Lin, Yi-Nan; Ma, Lang et al. (2011) Identification and characterization of RBM44 as a novel intercellular bridge protein. PLoS One 6:e17066
Roy, Angshumoy; Matzuk, Martin M (2011) Reproductive tract function and dysfunction in women. Nat Rev Endocrinol 7:517-25
Greenbaum, Michael P; Iwamori, Tokuko; Buchold, Gregory M et al. (2011) Germ cell intercellular bridges. Cold Spring Harb Perspect Biol 3:a005850
Hawkins, Shannon M; Buchold, Gregory M; Matzuk, Martin M (2011) Minireview: The roles of small RNA pathways in reproductive medicine. Mol Endocrinol 25:1257-79
Nalam, Roopa L; Matzuk, Martin M (2010) Local signalling environments and human male infertility: what we can learn from mouse models. Expert Rev Mol Med 12:e15

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