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A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21

Authors :
Yasuhiro Kazuki
Feng J Gao
Yicong Li
Anna J Moyer
Benjamin Devenney
Kei Hiramatsu
Sachiko Miyagawa-Tomita
Satoshi Abe
Kanako Kazuki
Naoyo Kajitani
Narumi Uno
Shoko Takehara
Masato Takiguchi
Miho Yamakawa
Atsushi Hasegawa
Ritsuko Shimizu
Satoko Matsukura
Naohiro Noda
Narumi Ogonuki
Kimiko Inoue
Shogo Matoba
Atsuo Ogura
Liliana D Florea
Alena Savonenko
Meifang Xiao
Dan Wu
Denise AS Batista
Junhua Yang
Zhaozhu Qiu
Nandini Singh
Joan T Richtsmeier
Takashi Takeuchi
Mitsuo Oshimura
Roger H Reeves
Source :
eLife, Vol 9 (2020)
Publication Year :
2020
Publisher :
eLife Sciences Publications Ltd, 2020.

Abstract

Animal models of Down syndrome (DS), trisomic for human chromosome 21 (HSA21) genes or orthologs, provide insights into better understanding and treatment options. The only existing transchromosomic (Tc) mouse DS model, Tc1, carries a HSA21 with over 50 protein coding genes (PCGs) disrupted. Tc1 is mosaic, compromising interpretation of results. Here, we “clone” the 34 MB long arm of HSA21 (HSA21q) as a mouse artificial chromosome (MAC). Through multiple steps of microcell-mediated chromosome transfer, we created a new Tc DS mouse model, Tc(HSA21q;MAC)1Yakaz (“TcMAC21”). TcMAC21 is not mosaic and contains 93% of HSA21q PCGs that are expressed and regulatable. TcMAC21 recapitulates many DS phenotypes including anomalies in heart, craniofacial skeleton and brain, molecular/cellular pathologies, and impairments in learning, memory and synaptic plasticity. TcMAC21 is the most complete genetic mouse model of DS extant and has potential for supporting a wide range of basic and preclinical research.

Details

Language :
English
ISSN :
2050084X
Volume :
9
Database :
Directory of Open Access Journals
Journal :
eLife
Publication Type :
Academic Journal
Accession number :
edsdoj.902bee1fcc954ec09607d3e505b90a1b
Document Type :
article
Full Text :
https://doi.org/10.7554/eLife.56223