Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9

Fang Yuan; Dongsheng Guo; Ge Gao; Yanli Liu; Yingying Xu; Yuhang Wu; Fan Yang; Xinrong Ke; Keyu Lai; Liangqing Hong; Yin xiong Li

doi:10.1016/j.scr.2017.08.016

Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9

Fang Yuan
, Dongsheng Guo
, Ge Gao
, Yanli Liu
, Yingying Xu
, Yuhang Wu
, Fan Yang
, Xinrong Ke
, Keyu Lai
, Liangqing Hong^*
, Yin xiong Li

^*Corresponding author for this work

University of Science and Technology of China
CAS - Guangzhou Institute of Biomedicine and Health
University of Chinese Academy of Sciences
The Third Affiliated Hospital of Sun Yat-sen University

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

The ATP-sensitive potassium channel is an octameric complex, and one of its subunits, namely Kir6.2, is encoded by the KCNJ11 gene. Mutations in KCNJ11 result in hyperinsulinism or diabetes mellitus, associated with abnormal insulin secretion. Here, using CRISPR/Cas9 editing, we established a homozygous mutant KCNJ11 cell line, WAe001-A-12, which was generated by a 62-bp deletion in the coding sequence of the human embryonic stem cell line H1. It was confirmed that this deletion in the KCNJ11 gene did not affect the protein expression levels of key pluripotent factors. Additionally, normal karyotype and differentiation potency were observed for the cell line.

Original language	English
Pages (from-to)	89-93
Number of pages	5
Journal	Stem Cell Research
Volume	24
DOIs	https://doi.org/10.1016/j.scr.2017.08.016
Publication status	Published - Oct 2017
Externally published	Yes

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10.1016/j.scr.2017.08.016

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@article{b593d1b755c448e1be33580301524742,

title = "Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9",

abstract = "The ATP-sensitive potassium channel is an octameric complex, and one of its subunits, namely Kir6.2, is encoded by the KCNJ11 gene. Mutations in KCNJ11 result in hyperinsulinism or diabetes mellitus, associated with abnormal insulin secretion. Here, using CRISPR/Cas9 editing, we established a homozygous mutant KCNJ11 cell line, WAe001-A-12, which was generated by a 62-bp deletion in the coding sequence of the human embryonic stem cell line H1. It was confirmed that this deletion in the KCNJ11 gene did not affect the protein expression levels of key pluripotent factors. Additionally, normal karyotype and differentiation potency were observed for the cell line.",

author = "Fang Yuan and Dongsheng Guo and Ge Gao and Yanli Liu and Yingying Xu and Yuhang Wu and Fan Yang and Xinrong Ke and Keyu Lai and Liangqing Hong and Li, \{Yin xiong\}",

note = "Publisher Copyright: {\textcopyright} 2017",

year = "2017",

month = oct,

doi = "10.1016/j.scr.2017.08.016",

language = "English",

volume = "24",

pages = "89--93",

journal = "Stem Cell Research",

issn = "1873-5061",

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}

TY - JOUR

T1 - Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9

AU - Yuan, Fang

AU - Guo, Dongsheng

AU - Gao, Ge

AU - Liu, Yanli

AU - Xu, Yingying

AU - Wu, Yuhang

AU - Yang, Fan

AU - Ke, Xinrong

AU - Lai, Keyu

AU - Hong, Liangqing

AU - Li, Yin xiong

PY - 2017/10

Y1 - 2017/10

N2 - The ATP-sensitive potassium channel is an octameric complex, and one of its subunits, namely Kir6.2, is encoded by the KCNJ11 gene. Mutations in KCNJ11 result in hyperinsulinism or diabetes mellitus, associated with abnormal insulin secretion. Here, using CRISPR/Cas9 editing, we established a homozygous mutant KCNJ11 cell line, WAe001-A-12, which was generated by a 62-bp deletion in the coding sequence of the human embryonic stem cell line H1. It was confirmed that this deletion in the KCNJ11 gene did not affect the protein expression levels of key pluripotent factors. Additionally, normal karyotype and differentiation potency were observed for the cell line.

AB - The ATP-sensitive potassium channel is an octameric complex, and one of its subunits, namely Kir6.2, is encoded by the KCNJ11 gene. Mutations in KCNJ11 result in hyperinsulinism or diabetes mellitus, associated with abnormal insulin secretion. Here, using CRISPR/Cas9 editing, we established a homozygous mutant KCNJ11 cell line, WAe001-A-12, which was generated by a 62-bp deletion in the coding sequence of the human embryonic stem cell line H1. It was confirmed that this deletion in the KCNJ11 gene did not affect the protein expression levels of key pluripotent factors. Additionally, normal karyotype and differentiation potency were observed for the cell line.

UR - https://www.scopus.com/pages/publications/85028074922

U2 - 10.1016/j.scr.2017.08.016

DO - 10.1016/j.scr.2017.08.016

M3 - Article

C2 - 29034901

AN - SCOPUS:85028074922

SN - 1873-5061

VL - 24

SP - 89

EP - 93

JO - Stem Cell Research

JF - Stem Cell Research

ER -

Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9

Abstract

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