4.8 Article

Bab2 Functions as an Ecdysone-Responsive Transcriptional Repressor during Drosophila Development

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CELL REPORTS
卷 32, 期 4, 页码 -

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CELL PRESS
DOI: 10.1016/j.celrep.2020.107972

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资金

  1. Swedish Research Council Vetenskapsradet [2015-05468, 2019-05249, 2018-04401]
  2. Austrian Science Fund FWF [P27183-B24]
  3. Knut and Alice Wallenberg Foundation [2017.0091]
  4. Stiftelsen Olle Engkvist Byggmastare [194-0681]
  5. National Basic Research Program of China [2015CB755703]
  6. National Natural Science Foundation of China [31672354, 31702057]
  7. Canadian Institutes of Health Research [MOP-114934]
  8. Swedish Research Council [2019-05249, 2018-04401] Funding Source: Swedish Research Council

向作者/读者索取更多资源

Drosophila development is governed by distinct ecdysone steroid pulses that initiate spatially and temporally defined gene expression programs. The translation of these signals into tissue-specific responses is crucial for metamorphosis, but the mechanisms that confer specificity to systemic ecdysone pulses are far from understood. Here, we identify Bric-a-brac 2 (Bab2) as an ecdysone-responsive transcriptional repressor that controls temporal gene expression during larval to pupal transition. Bab2 is necessary to terminate Salivary gland secretion (Sgs) gene expression, while premature Bab2 expression blocks Sgs genes and causes precocious salivary gland histolysis. The timely expression of bab2 is controlled by the ecdysone-responsive transcription factor Broad, and manipulation of EcR/USP/Broad signaling induces inappropriate Bab2 expression and termination of Sgs gene expression. Bab2 directly binds to Sgs loci in vitro and represses all Sgs genes in vivo. Our work characterizes Bab2 as a temporal regulator of somatic gene expression in response to systemic ecdysone signaling.

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