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10.1016/j.cell.2015.03.020

http://scihub22266oqcxt.onion/10.1016/j.cell.2015.03.020
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C4426339!4426339!25957684
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suck abstract from ncbi


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pmid25957684      Cell 2015 ; 161 (4): 762-73
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  • Non-coding RNA generated following lariat-debranching mediates targeting of AID to DNA #MMPMID25957684
  • Zheng S; Vuong BQ; Vaidyanathan B; Lin JY; Huang FT; Chaudhuri J
  • Cell 2015[May]; 161 (4): 762-73 PMID25957684show ga
  • Transcription through immunoglobulin switch (S) regions is essential for class switch recombination (CSR) but no molecular function of the transcripts has been described. Likewise, recruitment of activation-induced cytidine deaminase (AID) to S regions is critical for CSR; however, the underlying mechanism has not been fully elucidated. Here, we demonstrate that intronic switch RNA acts in trans to target AID to S region DNA. AID binds directly to switch RNA through G-quadruplexes formed by the RNA molecules. Disruption of this interaction by mutation of a key residue in the putative RNA-binding domain of AID impairs recruitment of AID to S region DNA, thereby abolishing CSR. Additionally, inhibition of RNA lariat processing leads to loss of AID localization to S regions and compromises CSR; both defects can be rescued by exogenous expression of switch transcripts in a sequence-specific manner. These studies uncover an RNA-mediated mechanism of targeting AID to DNA.
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