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A sustainable mouse karyotype created by programmed chromosome fusion.

Li-Bin WangZhi-Kun LiLe-Yun WangKai XuTian-Tian JiYi-Huan MaoSi-Nan MaTao LiuCheng-Fang TuQian ZhaoXu-Ning FanChao LiuLi-Ying WangYou-Jia ShuNing YangSunyang YingWei Li
Published in: Science (New York, N.Y.) (2022)
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.
Keyphrases
  • embryonic stem cells
  • copy number
  • gene expression
  • high fat diet
  • transcription factor
  • genome wide
  • metabolic syndrome
  • adipose tissue
  • molecular dynamics simulations
  • insulin resistance