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10.1016/j.celrep.2017.08.027

http://scihub22266oqcxt.onion/10.1016/j.celrep.2017.08.027
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C5705222!5705222!28854373
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suck abstract from ncbi


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pmid28854373      Cell+Rep 2017 ; 20 (9): 2262-76
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  • Genome-wide maps of m6A circRNAs identify widespread and cell-type-specific methylation patterns that are distinct from mRNAs #MMPMID28854373
  • Zhou C; Molinie B; Daneshvar K; Pondick JV; Wang J; Van Wittenberghe NO; Xing Y; Giallourakis CC; Mullen AC
  • Cell Rep 2017[Aug]; 20 (9): 2262-76 PMID28854373show ga
  • N6-methyladenosine (m6A) is the most abundant internal modification of mRNAs and is implicated in all aspects of post-transcriptional RNA metabolism. However, little is known about m6A modifications to circular (circ) RNAs. We developed a computational pipeline (AutoCirc) that together with depletion of ribosomal RNA and m6A immunoprecipitation defined thousands of m6A-circRNAs, with cell-type-specific expression. The presence of m6A-circRNAs is corroborated by interaction between circRNAs and YTHDF1/YTHDF2, proteins that read m6A sites in mRNAs, and by reduced m6A levels upon depletion of METTL3, the m6A writer. Despite sharing m6A readers and writers, m6A-circRNAs are frequently derived from exons that are not methylated in mRNAs, while mRNAs that are methylated on the same exons that compose m6A-circRNAs exhibit less stability, in a process regulated by YTHDF2. These results expand our understanding of the breadth of m6A modifications and uncover regulation of circRNAs through m6A modification.
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