4.7 Article

CLIP: Construction of cDNA libraries for high-throughput sequencing from RNAs cross-linked to proteins in vivo

期刊

METHODS
卷 48, 期 3, 页码 287-293

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2009.02.021

关键词

CLIP; UV cross-linking; Immunoprecipitation; RNA-protein binding; High-throughput sequencing

资金

  1. Medical Research Courtcil, UK
  2. European Research Council
  3. MRC [MC_U105185858] Funding Source: UKRI
  4. Medical Research Council [MC_U105185858] Funding Source: researchfish

向作者/读者索取更多资源

UV cross-linking and immunoprecipitation assay (CLIP) can identify direct interaction sites between RNA-binding proteins and RNAs in vivo, and has been used to study several proteins in tissues and cell cultures. The main challenge of the method is to specifically amplify the low amount of isolated RNA. The current protocol is optimised for efficient RNA purification and ligation of barcoded RNA adapters, High-throughput sequencing of the multiplexed cDNA library allows for a comprehensive coverage of the target sequences. (C) 2009 Elsevier Inc. All rights reserved.

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