Members of the HRT family of basic helix-loop-helix proteins act as transcriptional repressors downstream of Notch signaling

被引:191
作者
Nakagawa, O
McFadden, DG
Nakagawa, M
Yanagisawa, H
Hu, TH
Srivastava, D
Olson, EN
机构
[1] Univ Texas, SW Med Ctr, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Pediat, Dallas, TX 75390 USA
关键词
D O I
10.1073/pnas.250485597
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 Hairy-related transcription-factor (HRT) genes encode three related basic helix-loop-helix transcription factors that show sequence similarity to the Hairy and Enhancer of split family of transcriptional repressors. HRT proteins are expressed in specific regions of the developing heart, vasculature. pharyngeal arches and somites, and the periodicity of their expression in semitic precursors mirrors that of Notch signaling-related molecules. In the present study, we show that the intracellular domain of the Notch 1 receptor (Notch1 IC), which is constitutively active, up-regulates HRT2 expression in 10T(1)/(2) fibroblasts. Luciferase reporter assays using the regulatory regions of the mouse HRT genes revealed that transcription of all three genes is stimulated by Notch1 IC. The promoters of the HRT genes share homology in a binding site for Suppressor of Hairless [Su(H)], a transcriptional mediator of Notch signaling. A dominant-negative Su(H) mutant abolished Notch-activated HRT2 expression, and mutation of the conserved Su(H) consensus site in the HRT2 promoter attenuated transcriptional activation by Notch. Ectopic expression of HRT proteins also blocked activation of HRT2 expression by Notch1 IC through a mechanism requiring the basic region, but not the conserved carboxyl-terminal YQPW-TEVGAF motif of HRT2. These findings identify HRT genes as downstream targets for Notch signaling and reveal a negative autoregulatory loop whereby HRT proteins repress their own expression through interference with Notch signaling.
引用
收藏
页码:13655 / 13660
页数:6
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