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利用CRISPR/Cas9基因筛选研究细胞识别

Investigating Cellular Recognition Using CRISPR/Cas9 Genetic Screening.

作者信息

Chong Zheng-Shan, Wright Gavin J, Sharma Sumana

机构信息

Cell Surface Signalling Laboratory, Wellcome Sanger Institute, Cambridge CB10 1SA, UK.

Cell Surface Signalling Laboratory, Wellcome Sanger Institute, Cambridge CB10 1SA, UK.

出版信息

Trends Cell Biol. 2020 Aug;30(8):619-627. doi: 10.1016/j.tcb.2020.05.005. Epub 2020 Jun 25.

Abstract

Neighbouring cells can recognise and communicate with each other by direct binding between cell surface receptor and ligand pairs. Examples of cellular recognition events include pathogen entry into a host cell, sperm-egg fusion, and self/nonself discrimination by the immune system. Despite growing appreciation of cell surface recognition molecules as potential therapeutic targets, identifying key factors contributing to cellular recognition remains technically challenging to perform on a genome-wide scale. Recently, genome-scale clustered regularly interspaced short palindromic repeats (CRISPR) knockout or activation (CRISPR-KO/CRISPRa) screens have been applied to identify the molecular determinants of cellular recognition. In this review, we discuss how CRISPR-KO/CRISPRa screening has contributed to our understanding of cellular recognition processes, and how it can be applied to investigate these important interactions in a range of biological contexts.

摘要

相邻细胞可通过细胞表面受体与配体对之间的直接结合相互识别并进行通讯。细胞识别事件的例子包括病原体进入宿主细胞、精卵融合以及免疫系统的自我/非自我识别。尽管人们越来越认识到细胞表面识别分子作为潜在治疗靶点的重要性,但在全基因组范围内鉴定促成细胞识别的关键因素在技术上仍具有挑战性。最近,全基因组规模的成簇规律间隔短回文重复序列(CRISPR)敲除或激活(CRISPR-KO/CRISPRa)筛选已被用于鉴定细胞识别的分子决定因素。在本综述中,我们讨论了CRISPR-KO/CRISPRa筛选如何有助于我们理解细胞识别过程,以及它如何应用于在一系列生物学背景下研究这些重要的相互作用。

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