Manipulation of human minichromosomes to carry greater than megabase-sized chromosome inserts

被引:112
作者
Yoshimi, K
Tomizuka, K
Shinohara, T
Kazuki, Y
Yoshida, H
Ohguma, A
Yamamoto, T
Tanaka, S
Oshimura, M
Ishida, I
机构
[1] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Takasaki, Gumma 3701295, Japan
[2] Tottori Univ, Fac Med, Sch Life Sci, Dept Mol & Cell Genet, Tottori 6838503, Japan
关键词
chromosome cloning; human artificial chromosomes;
D O I
10.1038/80287
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
For introducing regions of human chromosomes greater than a megabase into cells or animals, we have developed a chromosome-cloning system in which defined regions of human chromosomes can be cloned into a stable human minichromosome vector in homologous recombination-proficient chicken DT40 cells. The stable minichromosome vector allowed a 10 Mb-sized region of the mitotically unstable human chromosome 22 to be stably maintained in mouse embryonic stem (ES) cells, and in mice. Furthermore, we demonstrated functional expression of human genes from the HAC in mice, This study describes a stable cloning and expression system for greater than megabase-sized regions of human chromosomes.
引用
收藏
页码:1086 / 1090
页数:5
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