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Publication : NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression.

First Author  Rajkovic A Year  2004
Journal  Science Volume  305
Issue  5687 Pages  1157-9
PubMed ID  15326356 Mgi Jnum  J:92421
Mgi Id  MGI:3052602 Doi  10.1126/science.1099755
Citation  Rajkovic A, et al. (2004) NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression. Science 305(5687):1157-9
abstractText  Primordial ovarian follicles in mice form when somatic cells surround individual oocytes. We show that lack of Nobox, an oocyte-specific homeobox gene, accelerates postnatal oocyte loss and abolishes the transition from primordial to growing follicles in mice. Follicles are replaced by fibrous tissue in female mice lacking Nobox in a manner similar to nonsyndromic ovarian failure in women. Genes preferentially expressed in oocytes, including Oct4 and Gdf9, are down-regulated in Nobox-/- mice, whereas ubiquitous genes such as Bmp4, Kit, and Bax remain unaffected. Therefore, Nobox is critical for specifying an oocyte-restricted gene expression pattern essential for postnatal follicle development.
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