Tpit-independent function of NeuroD1(BETA2) in pituitary corticotroph differentiation

被引:50
作者
Lamolet, B
Poulin, G
Chu, K
Guillemot, F
Tsai, MJ
Drouin, J
机构
[1] Inst Rech Clin Montreal, Genet Mol Lab, Montreal, PQ H2W 1R7, Canada
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Natl Inst Med Res, Div Mol Neurobiol, London NW7 1AA, England
关键词
D O I
10.1210/me.2003-0127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
NeuroD1(BETA2) and Tpit are cell-specific activators of pituitary proopiomelanocortin ( POMC) gene transcription. Expression of both factors slightly precedes that of POMC at embryonic d 12.5 of mouse pituitary development. We now report that NeuroD1( BETA2) is required for early corticotroph differentiation. In agreement with the transcriptional synergism observed between Tpit and basic helix-loop-helix dimers containing NeuroD1( BETA2), POMC expression is delayed in NeuroD1-deficient mice. However, this differentiation defect does not reflect a change of corticotroph commitment as revealed by Tpit expression. The delay of corticotroph terminal differentiation is transient and coincides with the developmental window of NeuroD1 expression in corticotrophs. In contrast to their requirement in other NeuroD1-expressing cells, the neurogenin genes do not appear to be necessary for corticotroph differentiation. Taken together with a similar requirement of Tpit for corticotroph differentiation but not for commitment, the present data indicate that the POMC promoter is a point of convergence for independent corticotroph differentiating signals.
引用
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页码:995 / 1003
页数:9
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