TY - JOUR
T1 - Systematic genome editing of the genes on zebrafish Chromosome 1 by CRISPR/Cas9
AU - and The ZAKOC Consortium
AU - Sun, Yonghua
AU - Zhang, Bo
AU - Luo, Lingfei
AU - Shi, De Li
AU - Wang, Han
AU - Cui, Zongbin
AU - Huang, Honghui
AU - Cao, Ying
AU - Shu, Xiaodong
AU - Zhang, Wenqing
AU - Zhou, Jianfeng
AU - Li, Yun
AU - Du, Jiulin
AU - Zhao, Qingshun
AU - Chen, Jun
AU - Zhong, Hanbing
AU - Zhong, Tao P.
AU - Li, Li
AU - Xiong, Jing Wei
AU - Peng, Jinrong
AU - Xiao, Wuhan
AU - Zhang, Jian
AU - Yao, Jihua
AU - Yin, Zhan
AU - Mo, Xianming
AU - Peng, Gang
AU - Zhu, Jun
AU - Chen, Yan
AU - Zhou, Yong
AU - Liu, Dong
AU - Pan, Weijun
AU - Zhang, Yiyue
AU - Ruan, Hua
AU - Liu, Feng
AU - Zhu, Zuoyan
AU - Meng, Anming
N1 - Publisher Copyright:
© 2020 Sun et al.
PY - 2020
Y1 - 2020
N2 - Genome editing by the well-established CRISPR/Cas9 technology has greatly facilitated our understanding of many biological processes. However, a complete whole-genome knockout for any species or model organism has rarely been achieved. Here, we performed a systematic knockout of all the genes (1333) on Chromosome 1 in zebrafish, successfully mutated 1029 genes, and generated 1039 germline-transmissible alleles corresponding to 636 genes. Meanwhile, by high-throughput bioinformatics analysis, we found that sequence features play pivotal roles in effective gRNA targeting at specific genes of interest, while the success rate of gene targeting positively correlates with GC content of the target sites. Moreover, we found that nearly one-fourth of all mutants are related to human diseases, and several representative CRISPR/Cas9-generated mutants are described here. Furthermore, we tried to identify the underlying mechanisms leading to distinct phenotypes between genetic mutants and antisense morpholino-mediated knockdown embryos. Altogether, this work has generated the first chromosome-wide collection of zebrafish genetic mutants by the CRISPR/Cas9 technology, which will serve as a valuable resource for the community, and our bioinformatics analysis also provides some useful guidance to design gene-specific gRNAs for successful gene editing.
AB - Genome editing by the well-established CRISPR/Cas9 technology has greatly facilitated our understanding of many biological processes. However, a complete whole-genome knockout for any species or model organism has rarely been achieved. Here, we performed a systematic knockout of all the genes (1333) on Chromosome 1 in zebrafish, successfully mutated 1029 genes, and generated 1039 germline-transmissible alleles corresponding to 636 genes. Meanwhile, by high-throughput bioinformatics analysis, we found that sequence features play pivotal roles in effective gRNA targeting at specific genes of interest, while the success rate of gene targeting positively correlates with GC content of the target sites. Moreover, we found that nearly one-fourth of all mutants are related to human diseases, and several representative CRISPR/Cas9-generated mutants are described here. Furthermore, we tried to identify the underlying mechanisms leading to distinct phenotypes between genetic mutants and antisense morpholino-mediated knockdown embryos. Altogether, this work has generated the first chromosome-wide collection of zebrafish genetic mutants by the CRISPR/Cas9 technology, which will serve as a valuable resource for the community, and our bioinformatics analysis also provides some useful guidance to design gene-specific gRNAs for successful gene editing.
UR - https://www.scopus.com/pages/publications/85078099434
U2 - 10.1101/gr.248559.119
DO - 10.1101/gr.248559.119
M3 - 文章
C2 - 31831591
AN - SCOPUS:85078099434
SN - 1088-9051
VL - 30
SP - 118
EP - 126
JO - Genome Research
JF - Genome Research
IS - 1
ER -