Post-doctoral Fellow

Post date: 3/11/19

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We use the mouse as a paradigm for investigating the developmental biology of mammalian gametogenesis and early embryogenesis. Our studies focus on molecular mechanisms of sex-specific factors that: 1) promote formation of ovulated eggs and mature spermatozoa; 2) ensure fertilization; and 3) support early development.

Gametogenesis: A hallmark of female germ cell development is asymmetric cell divisions during meiosis that result in large, ovulated eggs containing maternal factors necessary for early development. A hallmark of male germ cells is post-meiotic spermiogenesis in which round spermatids are transmogrified into mature, motile spermatozoa capable of fertilization. We have identified entrance points into genetic hierarchies that we exploit to investigate the networks that control these pathways.

Fertilization: Monospermic fertilization is essential for the onset of mammalian development. One sperm is required, but two are embryonic lethal. A major arbiter of this constricted window of opportunity is the zona pellucida that surrounds ovulated eggs and pre-implantation embryos. Molecular biology and gene-editing in mice are used to validate models of gamete recognition, learn more about cortical granule biology and investigate the maintenance of monospermy.

Early Development: We study the egg to embryo transition by investigating maternal effect genes that encode proteins required for pre-implantation development. We also investigate degradation of maternal proteins and RNA on which successful embryogenesis is dependent.

The lab occupies modern, well-equipped space on the Bethesda campus of the NIH replete with a procedure room in the vivarium with integrated systems for oocyte, pronuclear and blastocyst injections. The technologies necessary to carry out our research are well established and the presence of a highly experienced embryologist, an imaging technologist, and embedded bioinformatic support ensure success in making and analyzing the phenotype of transgenic and gene-edited mice. Mentoring is emphasized and fellows are expected to develop independence by pursing their projects to fruition during their training at the NIH.

About You

Ideal candidates will be trained in current DNA/RNA methodologies and have less than 5 years of postdoctoral experience.

Contact Dr. Jurrien DeanBack to All Jobs and Recruitment