Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition
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We thank Dr B Volgelstein Johns Hopkins University for providing HCT116-WT and HCT116-DKO cells [17]. We also thank Dr R Nagarajan University of California, San Francisco for ChIP-PCR primer sequences of SNRPN and GABRB3 regions, and Qingsong Tang NHLBI for assistance with GAII sequencing. The sequencing of RNA-Seq samples was performed by the DNA Sequencing and Genomics Core facility of NHLBI. This work was supported by the Intramural Research Program of the National Institutes of Health, National Heart, Lung, and Blood Institute KZ. AKM was additionally supported by a fellowship from the UGSP, National Institutes of Health
2013-11-29(万方平台首次上网日期,不代表论文的发表时间)
共14页
1256-1269