The transforming growth factor 2 (TGF2) superfamily of growth factors is the largest family of secreted proteins in mammals. These diverse ligands, which are synthesized as prepropeptides and processed to active dimers, function in essentially every developmental and physiologic process. Our HD33438 grant, "Analysis of Reproductive Function Using Transgenic Mice", has been funded by NICHD since 1996 and was the recipient of a MERIT award in 2001. Over this funding period, Dr. Matzuk (the Principal Investigator) and his laboratory have been productive leaders in the identification and characterization of the oocyte-secreted TGF2 family members, growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15). With the support of HD33438, we have published over 80 papers including a dozen papers in Nature, Nature Genetics, Nature Medicine, Science, and PLoS Biology. Whereas mammalian oocytes were initially postulated to be passengers rather than drivers in ovarian folliculogenesis, we demonstrated that GDF9 is essential for fertility at the primary follicle stage and plays critical roles at the pre-ovulatory follicle stage to regulate cumulus expansion. We also discovered the X-linked BMP15 gene and have characterized its functions in vitro and in vivo. These insights have helped to define the oocyte-somatic cell dialogue in ovarian folliculogenesis. The overall hypotheses of this renewal are that the oocyte-secreted proteins, GDF9 and BMP15, signal through specific ovarian granulosa cell type 1 receptors and downstream pathways to regulate oocyte maturation and fertilization and subsequent embryo development in mice and women and that TGF2 and microRNA pathways are linked in smooth muscle development in the female reproductive tract.
The Specific Aims of these proposed studies are: 1) Characterize the relationship of TGF2 and microRNA pathways in the development of oviductal and uterine smooth muscles;2) Identify the GDF9 type 1 receptor in granulosa cells;3) Determine the molecular aspects for receptor specificity of the BMP15 and GDF9 ligands;and 4) Study the BMP15 and GDF9 signaling pathways in human granulosa cells. These studies will not only accelerate the pace of research in the Matzuk laboratory but will also accelerate translational research in other United States laboratories including those of our Co-investigators, Drs. Mandy Katz-Jaffe and Thomas Thompson. At the end of this 5-year period, we expect to have unlocked key molecular events that are orchestrated by members of the TGF2family and drive human reproduction and that will ultimately facilitate efforts to optimize assisted reproductive technology procedures for women.

Public Health Relevance

Our studies are directly relevant to the mission of NICHD and in particular contraception, reproduction, and population research since TGF2 family members, including BMP15 and GDF9, play key roles in fertility in mammals including women. Our studies to define TGF2 family signaling pathways in the female reproductive tract will improve the reproductive health of women, better the quality-of-life of women and their offspring, improve the diagnosis and treatment of reproductive health conditions including infertility, and advance the development of better contraceptives for women.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD033438-18
Application #
8470194
Study Section
Integrative and Clinical Endocrinology and Reproduction Study Section (ICER)
Program Officer
Taymans, Susan
Project Start
1996-05-01
Project End
2016-05-31
Budget Start
2013-06-01
Budget End
2014-05-31
Support Year
18
Fiscal Year
2013
Total Cost
$397,317
Indirect Cost
$88,772
Name
Baylor College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Peng, Jia; Li, Qinglei; Wigglesworth, Karen et al. (2013) Growth differentiation factor 9:bone morphogenetic protein 15 heterodimers are potent regulators of ovarian functions. Proc Natl Acad Sci U S A 110:E776-85
Wigglesworth, Karen; Lee, Kyung-Bon; O'Brien, Marilyn J et al. (2013) Bidirectional communication between oocytes and ovarian follicular somatic cells is required for meiotic arrest of mammalian oocytes. Proc Natl Acad Sci U S A 110:E3723-9
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
Li, Qinglei; Agno, Julio E; Edson, Mark A et al. (2011) Transforming growth factor ? receptor type 1 is essential for female reproductive tract integrity and function. PLoS Genet 7:e1002320
Su, You-Qiang; Sugiura, Koji; Li, Qinglei et al. (2010) Mouse oocytes enable LH-induced maturation of the cumulus-oocyte complex via promoting EGF receptor-dependent signaling. Mol Endocrinol 24:1230-9
Nalam, Roopa L; Lin, Yi-Nan; Matzuk, Martin M (2010) Testicular cell adhesion molecule 1 (TCAM1) is not essential for fertility. Mol Cell Endocrinol 315:246-53
Andreu-Vieyra, Claudia V; Chen, Ruihong; Agno, Julio E et al. (2010) MLL2 is required in oocytes for bulk histone 3 lysine 4 trimethylation and transcriptional silencing. PLoS Biol 8:
Edson, Mark A; Lin, Yi-Nan; Matzuk, Martin M (2010) Deletion of the novel oocyte-enriched gene, Gpr149, leads to increased fertility in mice. Endocrinology 151:358-68
Li, Qinglei; Rajanahally, Saneal; Edson, Mark A et al. (2009) Stable expression and characterization of N-terminal tagged recombinant human bone morphogenetic protein 15. Mol Hum Reprod 15:779-88
Souza, Danielle G; Amaral, Flavio A; Fagundes, Caio T et al. (2009) The long pentraxin PTX3 is crucial for tissue inflammation after intestinal ischemia and reperfusion in mice. Am J Pathol 174:1309-18

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