4.6 Article

The Global Regulatory Architecture of Transcription during the Caulobacter Cell Cycle

期刊

PLOS GENETICS
卷 11, 期 1, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1004831

关键词

-

资金

  1. Stanford graduate fellowship
  2. DOE [DOE-FG02-05ER64136]
  3. NSF [CCF 1344284]
  4. NIH [F32 GM100732, R01 GM51426, R01 GM32506]
  5. Stanford Vice Provost for Undergraduate Education Research Experience for Undergraduates (VPUE-REU) Program
  6. Stanford CURIS undergraduate research fellowship
  7. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [T32HG000044] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM051426, R01GM032506, F32GM100732] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Each Caulobacter cell cycle involves differentiation and an asymmetric cell division driven by a cyclical regulatory circuit comprised of four transcription factors (TFs) and a DNA methyltransferase. Using a modified global 59 RACE protocol, we globally mapped transcription start sites (TSSs) at base-pair resolution, measured their transcription levels at multiple times in the cell cycle, and identified their transcription factor binding sites. Out of 2726 TSSs, 586 were shown to be cell cycle-regulated and we identified 529 binding sites for the cell cycle master regulators. Twenty-three percent of the cell cycle-regulated promoters were found to be under the combinatorial control of two or more of the global regulators. Previously unknown features of the core cell cycle circuit were identified, including 107 antisense TSSs which exhibit cell cycle-control, and 241 genes with multiple TSSs whose transcription levels often exhibited different cell cycle timing. Cumulatively, this study uncovered novel new layers of transcriptional regulation mediating the bacterial cell cycle.

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

4.6
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