Home CAS Center for Excellence
  
  
  
 
Highlights/News
Seminars
Conferences
Media Reports
Jobs
Search
 
Address: 320 Yue Yang Road, Shanghai 200031, P.R. China
Tel: 86-21-54920000
Fax: 86-21-54921011
Email: sibcb@sibs.ac.cn
Website: www.sibcb.ac.cn
 
Haploid Embryonic Stem Cells, a Sperm Replacement Enabling Genetic Screening in Mice
 
Viewed: 1048
 

In 2012, a research group led by Profs. LI Jinsong and XU Guoliang published a Cell paper reporting the creation of androgenetic haploid embryonic stem cells (AG-haESCs) that can support full-term embryonic development upon injection into MII oocytes, leading to the generation of semi-cloned (SC) mice (Cell, 2012, 149: 605-617.). This study represented an important conceptual advance by the creation of a novel, renewable/culturable form of fertilization agent. Nevertheless, one major drawback of the previous work is the frequently observed aberrant development of AG-haESC-derived embryos and the very low birth rate of healthy SC mice (around 2% of total SC embryos); this greatly restricts the applications of AG-haESCs.

On July 9th, a team of researchers from Shanghai Institutes for Biological Sciences, led by LI Jinsong, WU Yuxuan of the Institute of Biochemistry and Cell Biology, and YANG Li of CAS-MPG Partner Institute for Computational Biology, have shown that AG-haESCs carrying deletions in the DMRs (differentially DNA methylated regions) controlling two paternally repressed imprinted genes, H19 and Gtl2, designated as DKO-AG-haESCs, can efficiently support the generation of SC pups at a rate of 20%.

Moreover, ZHONG Cuiqing, YIN Qi, XIE Zhengfei, BAI Meizhu, DONG Rui and their colleagues demonstrate that manipulation of multiple genes is feasible in DKO-AG-haESCs, leading to the generation of SC mice carrying multiple genetic traits at an appropriate efficiency.

Importantly, they further demonstrate that by combination of CRISPR-Cas9 library and DKO-AG-haESCs, SC mice carrying different mutant genes can be efficiently generated in one step, thus enabling functional mutagenic screening at organism level in mice, which can be done currently in lower organisms, such as yeast and C. elegans.

The researchers propose that this new technology is feasible for medium-scale targeted screening at organism level, especially for developmental phenotypes, using the appropriate sgRNA libraries targeting preselected candidate genes.

This work entitled “CRISPR-Cas9-Mediated Genetic Screening in Mice with Haploid Embryonic Stem Cells Carrying a Guide RNA Library” has been published online in Cell Stem Cell on July 9th.

This study was supported by the grants from the Chinese Academy of Sciences (the Strategic Priority Research Program), the Ministry of Science and Technology of China, the National Natural Science Foundation of China and the Science and Technology Commission of Shanghai Municipality.

AUTHOR CONTACT:
LI Jinsong, Principal Investigator
Institute of Biochemistry and Cell Biology, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences
Shanghai 200031, P. R. China
E-mail: jsli@sibcb.ac.cn


Information for the image (Graphic Abstract)
Combined application of altered expression of two imprinted genes and CRISPR-Cas9-based genome editing allows the efficient and stable generation of gene-modified semi-cloned mice from androgenetic haploid embryonic stem cells. This approach has potential for mutagenesis and screening.
(Image provided by Prof. LI Jinsong`s group)

 

Copyright © 2017-2020 Shanghai Institute of Biochemistry and Cell Biology, CAS. All rights reserved