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Non-coding RNA Generated following Lariat Debranching Mediates Targeting of AID to DNA
Author(s) -
Simin Zheng,
Bao Q. Vuong,
Bharat Vaidyanathan,
Jiayu Lin,
FengTing Huang,
Jayanta Chaudhuri
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.03.020
Subject(s) - biology , cytidine deaminase , rna , non coding rna , activation induced (cytidine) deaminase , dna , microbiology and biotechnology , transcription (linguistics) , rna editing , genetics , intron , immunoglobulin class switching , gene , antibody , linguistics , philosophy , b cell
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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