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Megabase-scale deletion using CRISPR/Cas9 to generate a fully haploid human cell line.

作者信息

Essletzbichler Patrick, Konopka Tomasz, Santoro Federica, Chen Doris, Gapp Bianca V, Kralovics Robert, Brummelkamp Thijn R, Nijman Sebastian M B, Bürckstümmer Tilmann

机构信息

Haplogen GmbH, 1030 Vienna, Austria;

Research Center for Molecular Medicine of the Austrian Academy of Sciences (CeMM), 1090 Vienna, Austria;

出版信息

Genome Res. 2014 Dec;24(12):2059-65. doi: 10.1101/gr.177220.114. Epub 2014 Nov 4.


DOI:10.1101/gr.177220.114
PMID:25373145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4248322/
Abstract

Near-haploid human cell lines are instrumental for genetic screens and genome engineering as gene inactivation is greatly facilitated by the absence of a second gene copy. However, no completely haploid human cell line has been described, hampering the genetic accessibility of a subset of genes. The near-haploid human cell line HAP1 contains a single copy of all chromosomes except for a heterozygous 30-megabase fragment of Chromosome 15. This large fragment encompasses 330 genes and is integrated on the long arm of Chromosome 19. Here, we employ a CRISPR/Cas9-based genome engineering strategy to excise this sizeable chromosomal fragment and to efficiently and reproducibly derive clones that retain their haploid state. Importantly, spectral karyotyping and single-nucleotide polymorphism (SNP) genotyping revealed that engineered-HAPloid (eHAP) cells are fully haploid with no gross chromosomal aberrations induced by Cas9. Furthermore, whole-genome sequence and transcriptome analysis of the parental HAP1 and an eHAP cell line showed that transcriptional changes are limited to the excised Chromosome 15 fragment. Together, we demonstrate the feasibility of efficiently engineering megabase deletions with the CRISPR/Cas9 technology and report the first fully haploid human cell line.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/c8f185242bc2/2059fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/b05a2b836824/2059fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/2acabc43257f/2059fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/50db2ec6289e/2059fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/c8f185242bc2/2059fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/b05a2b836824/2059fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/2acabc43257f/2059fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/50db2ec6289e/2059fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d7/4248322/c8f185242bc2/2059fig4.jpg

相似文献

[1]
Megabase-scale deletion using CRISPR/Cas9 to generate a fully haploid human cell line.

Genome Res. 2014-12

[2]
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[3]
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[4]
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[6]
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[7]
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[10]
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[4]
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[5]
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[6]
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本文引用的文献

[1]
Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencing.

Cell Stem Cell. 2014-7-3

[2]
Characterization of genomic deletion efficiency mediated by clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 nuclease system in mammalian cells.

J Biol Chem. 2014-8-1

[3]
Genome-wide analysis reveals characteristics of off-target sites bound by the Cas9 endonuclease.

Nat Biotechnol. 2014-5-18

[4]
Targeted genomic rearrangements using CRISPR/Cas technology.

Nat Commun. 2014-4-24

[5]
Genome engineering of mammalian haploid embryonic stem cells using the Cas9/RNA system.

PeerJ. 2013-12-23

[6]
Genetic modification and screening in rat using haploid embryonic stem cells.

Cell Stem Cell. 2013-12-19

[7]
Genetic screens in human cells using the CRISPR-Cas9 system.

Science. 2013-12-12

[8]
Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases.

Genome Res. 2013-11-19

[9]
A reversible gene trap collection empowers haploid genetics in human cells.

Nat Methods. 2013-8-25

[10]
Cas9 as a versatile tool for engineering biology.

Nat Methods. 2013-10

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