4.8 Article

Dynamic modulation of enhancer responsiveness by core promoter elements in living Drosophila embryos

期刊

NUCLEIC ACIDS RESEARCH
卷 50, 期 1, 页码 92-107

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkab1177

关键词

-

资金

  1. Japan Society for the Promotion of Science [18H06040, 20K15710, 21K20627]
  2. Ministry of Education, Culture, Sports, Science and Technology in Japan
  3. Tomizawa Jun-ichi & Keiko Fund of Molecular Biology Society of Japan for Young Scientist
  4. Mochida Memorial Foundation for Medical and Pharmaceutical Research
  5. Nakajima Foundation
  6. Inamori Foundation
  7. Takeda Science Foundation
  8. Sumitomo Foundation
  9. Senri Life Science Foundation
  10. Mitsubishi Foundation
  11. University of Tokyo
  12. JST, ACT-X [JPMJAX211J]
  13. MINECO-Feder [FPI2015/074837]
  14. University of Granada
  15. [21H05742]
  16. [20H05357]
  17. [19H03154]
  18. [19K22378]
  19. Grants-in-Aid for Scientific Research [21K20627, 20K15710, 18H06040] Funding Source: KAKEN

向作者/读者索取更多资源

Core promoter elements have differential effects on regulating functional parameters of transcriptional bursting in developing Drosophila embryos, including controlling the timing, continuity, and amplitude of bursts. While TATA affects burst amplitude, lnr, MTE, and DPE mainly influence burst frequency. Additionally, core promoter elements play a crucial role in establishing body segments in early embryos.
Regulatory interactions between enhancers and core promoters are fundamental for the temporal and spatial specificity of gene expression in development. The central role of core promoters is to initiate productive transcription in response to enhancer's activation cues. However, it has not been systematically assessed how individual core promoter elements affect the induction of transcriptional bursting by enhancers. Here, we provide evidence that each core promoter element differentially modulates functional parameters of transcriptional bursting in developing Drosophila embryos. Quantitative live imaging analysis revealed that the timing and the continuity of burst induction are common regulatory steps on which core promoter elements impact. We further show that the upstream TATA also affects the burst amplitude. On the other hand, lnr, MTE and DPE mainly contribute to the regulation of the burst frequency. Genome editing analysis of the pair-rule gene fushi tarazu revealed that the endogenous TATA and DPE are both essential for its correct expression and function during the establishment of body segments in early embryos. We suggest that core promoter elements serve as a key regulatory module in converting enhancer activity into transcription dynamics during animal development.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据