clip seq紫外交聯(lián)的作用

CLIP-seq,又稱(chēng)為HITS-CLIP，即紫外交聯(lián)免疫沉淀結(jié)合高通量測(cè)序(crosslinking-immunoprecipitation and high-throughput sequencing), 是一項(xiàng)在全基因組水平揭示RNA分子與RNA結(jié)合蛋白相互作用的革命性技術(shù)。

其主要原理是基于RNA分子與RNA結(jié)合蛋白在紫外照射下發(fā)生耦聯(lián)，以RNA結(jié)合蛋白的特異性抗體將RNA-蛋白質(zhì)復(fù)合體沉淀之后，回收其中的RNA片段，經(jīng)添加接頭、RT-PCR等步驟，對(duì)這些分子進(jìn)行高通量測(cè)序，再經(jīng)生物信息學(xué)的分析和處理、總結(jié)，挖掘出其特定規(guī)律，從而深入揭示RNA結(jié)合蛋白與RNA分子的調(diào)控作用及其對(duì)生命的意義。

Cross-Linking and Immunoprecipitation (CLIP)

Cross-Linking and Immunoprecipitation (CLIP) is an antibody-based technique used to study RNA-protein interactions related to RNA immunoprecipitation (RIP), but differs from RIP in the use of UV radiation to cross-link RNA and the binding proteins. Unlike DNA-protein crosslinking which is done with formaldehyde, CLIP uses ultraviolet (UV) light and the crosslinking is irreversible. UV crosslinks are also more specific and only link proteins to RNAs that are in very close proximity. Further, UV crosslinks do not form between two proteins. For these reasons, UV has become the standard in RNA research. The RNA-RBP complexes are then immunoprecipitated. Due to the irreversibility of the crosslinks, the next step is digestion with a proteinase.

UV crosslinking immunoprecipitation (CLIP) is an increasingly popular technique to study protein-RNA interactions in tissues and cells. Whole cells or tissues are ultraviolet irradiated to generate a covalent bond between RNA and proteins that are in close contact. After partial RNase digestion, antibodies specific to an RNA binding protein (RBP) or a protein-epitope tag is then used to immunoprecipitate the protein-RNA complexes. After stringent washing and gel separation the RBP-RNA complex is excised. The RBP is protease digested to allow purification of the bound RNA. Reverse transcription of the RNA followed by high-throughput sequencing of the cDNA library is now often used to identify protein bound RNA on a genome-wide scale. UV irradiation can result in cDNA truncations and/or mutations at the crosslink sites, which complicates the alignment of the sequencing library to the reference genome and the identification of the crosslinking sites. Meanwhile, one or more amino acids of a crosslinked RBP can remain attached to its bound RNA due to incomplete digestion of the protein. As a result, reverse transcriptase may not read through the crosslink sites, and produce cDNA ending at the crosslinked nucleotide. This is harnessed by one variant of CLIP methods to identify crosslinking sites at a nucleotide resolution. This method, individual nucleotide resolution CLIP (iCLIP) circularizes cDNA to capture the truncated cDNA and also increases the efficiency of ligating sequencing adapters to the library. Here, we describe the detailed procedure of iCLIP.