A sustainable mouse karyotype created by programmed chromosome fusion

Author:

Wang Li-Bin123ORCID,Li Zhi-Kun123ORCID,Wang Le-Yun123ORCID,Xu Kai123ORCID,Ji Tian-Tian14ORCID,Mao Yi-Huan123,Ma Si-Nan15,Liu Tao6,Tu Cheng-Fang6,Zhao Qian6,Fan Xu-Ning6,Liu Chao123,Wang Li-Ying1,Shu You-Jia14,Yang Ning14,Zhou Qi123ORCID,Li Wei123ORCID

Affiliation:

1. State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.

2. Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.

3. Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.

4. University of Chinese Academy of Sciences, Beijing 100049, China.

5. College of Life Science, Northeast Agricultural University, Harbin 150030, China.

6. Annoroad Gene Technology (Beijing) Co., Ltd., Beijing 100176, China.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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