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A sustainable mouse karyotype created by programmed chromosome fusion.
Wang, Li-Bin; Li, Zhi-Kun; Wang, Le-Yun; Xu, Kai; Ji, Tian-Tian; Mao, Yi-Huan; Ma, Si-Nan; Liu, Tao; Tu, Cheng-Fang; Zhao, Qian; Fan, Xu-Ning; Liu, Chao; Wang, Li-Ying; Shu, You-Jia; Yang, Ning; Zhou, Qi; Li, Wei.
Affiliation
  • Wang LB; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Li ZK; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
  • Wang LY; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
  • Xu K; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Ji TT; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
  • Mao YH; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
  • Ma SN; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Liu T; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
  • Tu CF; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
  • Zhao Q; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Fan XN; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
  • Liu C; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
  • Wang LY; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Shu YJ; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Yang N; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
  • Zhou Q; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
  • Li W; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Science ; 377(6609): 967-975, 2022 08 26.
Article in En | MEDLINE | ID: mdl-36007034
Chromosome engineering has been attempted successfully in yeast but remains challenging in higher eukaryotes, including mammals. Here, we report programmed chromosome ligation in mice that resulted in the creation of new karyotypes in the lab. Using haploid embryonic stem cells and gene editing, we fused the two largest mouse chromosomes, chromosomes 1 and 2, and two medium-size chromosomes, chromosomes 4 and 5. Chromatin conformation and stem cell differentiation were minimally affected. However, karyotypes carrying fused chromosomes 1 and 2 resulted in arrested mitosis, polyploidization, and embryonic lethality, whereas a smaller fused chromosome composed of chromosomes 4 and 5 was able to be passed on to homozygous offspring. Our results suggest the feasibility of chromosome-level engineering in mammals.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Artificial Gene Fusion / Karyotype / Gene Editing Limits: Animals Language: En Journal: Science Year: 2022 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Artificial Gene Fusion / Karyotype / Gene Editing Limits: Animals Language: En Journal: Science Year: 2022 Document type: Article Affiliation country: China Country of publication: United States