B cell development and immunoglobulin transcription in Oct-1-deficient mice

被引:34
作者
Wang, VEH
Tantin, D
Chen, JZ
Sharp, PA
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Canc Res Ctr, Cambridge, MA 02139 USA
[3] MIT, McGovern Inst, Cambridge, MA 02139 USA
关键词
D O I
10.1073/pnas.0307304101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The POU domain transcription factors Oct-1 and Oct-2 interact with the octamer element, a motif conserved within Ig promoters and enhancers, and mediate transcription from the Ig loci. Inactivation of Oct-2 by gene targeting results in normal B cell development and 19 transcription. To study the role of Oct-1 in these processes, the lymphoid compartment of RAG-1-1(-/-) animals was reconstituted with Oct-1-deficient fetal liver hematopoietic cells. Recipient mice develop B cells with levels of surface Ig expression comparable with wild type, although at slightly reduced numbers. These B cells transcribe Ig normally, respond to antigenic stimulation, undergo class switching, and use a normal repertoire of light chain variable segments. However, recipient mice show slight reductions in serum IgM and IgA. Thus, the Oct-1 protein is dispensable for B cell development and Ig transcription.
引用
收藏
页码:2005 / 2010
页数:6
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