| Literature DB >> 21036187 |
Michael Hampsey1, Badri Nath Singh, Athar Ansari, Jean-Philippe Lainé, Shankarling Krishnamurthy.
Abstract
Gene loops are dynamic structures that juxtapose promoter–terminator regions of Pol II-transcribed genes. Although first described in yeast, gene loops have now been identified in yeast and mammalian cells. Looping requires components of the transcription preinitiation complex, the pre-mRNA 30-end processing machinery, and subunits of the nuclear pore complex. Loop formation is transcription-dependent, but neither basal nor activated transcription requires looping. Rather, looping appears to affect cellular memory of recent transcriptional activity, enabling a more rapid response to subsequent stimuli. The nuclear pore has been implicated in both memory and looping. Our working model is that loops are formed and/or maintained at the nuclear pore to facilitate hand-off of Pol II form the terminator to the promoter, thereby bypassing Pol II recruitment as the rate-limiting step in reactivation of transcription. Involvement of the nuclear pore also suggests that looping might facilitate mRNA export to the cytoplasm. The technology now exists to test these ideas.Entities:
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Year: 2010 PMID: 21036187 PMCID: PMC3305805 DOI: 10.1016/j.advenzreg.2010.10.001
Source DB: PubMed Journal: Adv Enzyme Regul ISSN: 0065-2571