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CRISPR系统可对必需基因和基因家族进行基因工程操作。

A CRISPR system permits genetic engineering of essential genes and gene families.

作者信息

Vyas Valmik K, Barrasa M Inmaculada, Fink Gerald R

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA ; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

出版信息

Sci Adv. 2015;1(3):e1500248. doi: 10.1126/sciadv.1500248.

Abstract

is a pathogenic yeast that causes mucosal and systematic infections with high mortality. The absence of facile molecular genetics has been a major impediment to analysis of pathogenesis. The lack of meiosis coupled with the absence of plasmids makes genetic engineering cumbersome, especially for essential functions and gene families. We describe a CRISPR system that overcomes many of the obstacles to genetic engineering in this organism. The high frequency with which CRISPR-induced mutations can be directed to target genes enables easy isolation of homozygous gene knockouts, even without selection. Moreover, the system permits the creation of strains with mutations in multiple genes, gene families, and genes that encode essential functions. This CRISPR system is also effective in a fresh clinical isolate of undetermined ploidy. Our method transforms the ability to manipulate the genome of and provides a new window into the biology of this pathogen.

摘要

是一种致病性酵母,可引起粘膜和全身性感染,死亡率很高。缺乏简便的分子遗传学方法一直是分析其发病机制的主要障碍。减数分裂的缺失加上质粒的缺乏使得基因工程变得繁琐,特别是对于必需功能和基因家族而言。我们描述了一种CRISPR系统,该系统克服了在这种生物体中进行基因工程的许多障碍。CRISPR诱导的突变可以高频靶向目标基因,即使不进行选择也能轻松分离纯合基因敲除。此外,该系统允许创建在多个基因、基因家族和编码必需功能的基因中具有突变的菌株。这种CRISPR系统在一个未确定倍性的新鲜临床分离株中也有效。我们的方法改变了操纵其基因组的能力,并为这种病原体的生物学研究提供了一个新窗口。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eec/4640623/302819844d39/1500248-F1.jpg

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