在DNA上CLOCK:BMAL1复合体的并联协会使CBP/p300通过多价值相互作用的招募成为可能
Diksha Sharma1, Lisa Stoos2, Megan R Torgrimson1
1Department of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, CA USA.
bioRxiv : the preprint server for biology
|September 15, 2025
概括
双联电子盒允许CLOCK:BMAL1转录因子结合核细胞,促进基因表达. 与CBP联合激活剂的多价值相互作用对于这种强大的昼夜节律至关重要.
科学领域:
- 分子生物学分子生物学
- 时间生物学 时间生物学
- 遗传学 是一个遗传学.
背景情况:
- CLOCK:BMAL1转录因子复合体调节昼夜基因表达.
- 强大的昼夜振荡取决于目标基因中的双联E-box动机.
研究的目的:
- 为了研究串联电子盒如何促进CLOCK:BMAL1与核细胞结合.
- 阐明CBP/p300联合激活剂相互作用在CLOCK:BMAL1活性中的作用.
主要方法:
- 染色体免疫沉试验用于评估 CLOCK:BMAL1 的结合性.
- 生物化学试验用于研究BMAL1和CBP之间的蛋白质-蛋白质相互作用.
- 记者测试测量CLOCK:BMAL1驱动的转录活动.
主要成果:
- 协同使用的E-box可以使更深的CLOCK:BMAL1结合到核体中,释放DNA.
- 这促进了与CBP联合激活剂的多价值相互作用.
- BMAL1的交易激活域与多个CBP域相互作用,对活动至关重要.
结论:
- 多价值CBP相互作用是tandem CLOCK:BMAL1异构体招募这种限制性辅因子的关键.
- 电子盒的结构安排影响了核细胞的可访问性和协作激活剂的招募.
- 这种机制有助于强大的昼夜基因表达模式.
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