Sox2: An essential factor for maintaining neural stem cells
The SoxB1 subfamily members, Sox1, Sox2, and Sox3, are coexpressed in neural stem cells and progenitor cells in the developing brain. Gene-targeting technology was utilized to study the role of Sox1 and Sox3 in the developing central nervous system. The results of inactivation of Sox1 and Sox3 in mutant mice suggest redundancy within the developing brain tissues among SoxB1 family members. The role of transcription factor Sox2 was investigated specifically in the developing brain by crossing the floxed Sox2 conditional knockout mice (RBRC01897) with neural stem/progenitor cell-specific Cre mice. Homozygous mutant mice had enlarged lateral ventricles and a reduced number of neurosphere-forming cells at a late embryonic stage, and died soon after birth. This strain is useful for studying the function of the Sox2 gene in various Sox2-positive tissues such as developing brain by crossing tissue-specific Cre transgenic mice.
|Related strain||:||SRR2-Bgeo transgenic mice RBRC01302 (visualizing neural stem/progenitor cells residing in restricted areas of the telencephalon)|
|Depositor||:||Dr. Akihiko Okuda, Saitama Medical University|
|References||:||1.||Miyagi S et al. Consequence of the loss of Sox2 in the developing brain of the mouse.FEBS Lett 582, 2811-2815, 2008.|
|2.||Miyagi S et al. The Sox2 regulatory region 2 functions as a neural stem cell-specific enhancer in the telencephalon. J Biol Chem 281, 13374-13381, 2006.|
|3.||Miyagi S et al. The Sox-2 regulatory regions display their activities in two distinct types of multipotent stem cells. Mol Cell Biol 24, 4207-4220, 2004.|