4.8 Article

RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo

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NATURE GENETICS
卷 39, 期 12, 页码 1512-1516

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NATURE PUBLISHING GROUP
DOI: 10.1038/ng.2007.26

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  1. Intramural NIH HHS [Z01 ES101987-02] Funding Source: Medline
  2. NHGRI NIH HHS [R01 HG004037, R01 HG004037-01A1, HG002668, R01 HG002668] Funding Source: Medline
  3. NIGMS NIH HHS [GM34431, R01 GM069676, R37 GM046638, GM069676, R01 GM046638] Funding Source: Medline

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It is widely assumed that the key rate-limiting step in gene activation is the recruitment of RNA polymerase II ( Pol II) to the core promoter(1). Although there are well-documented examples in which Pol II is recruited to a gene but stalls(2-12), a general role for Pol II stalling in development has not been established. We have carried out comprehensive Pol II chromatin immunoprecipitation microarray ( ChIP-chip) assays in Drosophila embryos and identified three distinct Pol II binding behaviors: active ( uniform binding across the entire transcription unit), no binding, and stalled ( binding at the transcription start site). The notable feature of the similar to 10% genes that are stalled is that they are highly enriched for developmental control genes, which are either repressed or poised for activation during later stages of embryogenesis. We propose that Pol II stalling facilitates rapid temporal and spatial changes in gene activity during development.

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