The Primate Embryo Gene Expression Resource (PREGER) advances the biology of nonhuman primate (NHP) and human oocytes and embryos, recognizing the significant limitations of rodent and other models to inform us about key aspects of human reproductive biology. PREGER overcomes the severe cost limitations of nonhuman primate oocyte and embryo biology and the legal and ethical restrictions associated with human studies, and have dramatically increased our understanding of nonhuman primate &human oocytes and embryos. PREGER provides to a growing set of users worldwide (1) an extensive set of >200 cDNA libraries, plus molecular reagents, methodologies, databases, and other resources to advance research in NHP embryology. (2) a large and expanding gene expression database base related to NHP embryogenesis and molecular determinants of oocyte and embryo quality, (3) specialized molecular services to the reproductive biology community, and (4) specialized training to expand the number of investigators in the field, 25% of whom have been clinically oriented scientists. In this proposal we request support to continue providing libraries and other reagents, as well as services to those scientists who require access to these specialized collections of materials and methods, which are applicable to studying primate and mammalian oocytes and embryos. We will also expand the database resource to include a new reproductive toxicology database, which will facilitate studies of endocrine disrupting and obesogen compounds of great interest to the National Toxicology Program for potential roles in developmental origins of human disease. We will also develop a new biofunction pathways database linking genes to cellular processes, and develop a crucially important new protein expression database to accompany mRNA expression data. Links will also be made to other databases related to human disease. Last, we will continue a summer course and expand the human resource development component by producing online instructional videos. Through these activities PREGER will continue to provide a highly productive, unique, and innovative resource with strong translational relevance.

Public Health Relevance

Molecular studies of gene expression in primate oocytes and embryos provide unique information for addressing human reproductive health &fertility. It is also useful for evaluating risks related to environmental factors and developmental origins of adult human disease. PREGER provides essential reagents, services, databases, and training to advance human reproductive health research.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Resource-Related Research Projects (R24)
Project #
3R24OD012221-13S1
Application #
8898965
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Program Officer
Mirochnitchenko, Oleg
Project Start
2000-09-30
Project End
2016-11-30
Budget Start
2014-08-18
Budget End
2014-11-30
Support Year
13
Fiscal Year
2014
Total Cost
$233,699
Indirect Cost
$36,525
Name
Michigan State University
Department
Veterinary Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Chaffin, Charles L; Latham, Keith E; Mtango, Namdori R et al. (2014) Dietary sugar in healthy female primates perturbs oocyte maturation and in vitro preimplantation embryo development. Endocrinology 155:2688-95
Hao, Lanping; Midic, Uros; Garriga, Judith et al. (2014) Contribution of CBX4 to cumulus oophorus cell phenotype in mice and attendant effects in cumulus cell cloned embryos. Physiol Genomics 46:66-80
Cheng, Yong; Gaughan, John; Midic, Uros et al. (2013) Systems genetics implicates cytoskeletal genes in oocyte control of cloned embryo quality. Genetics 193:877-96
Romasko, Edward J; Amarnath, Dasari; Midic, Uros et al. (2013) Association of maternal mRNA and phosphorylated EIF4EBP1 variants with the spindle in mouse oocytes: localized translational control supporting female meiosis in mammals. Genetics 195:349-58