ANALYSIS OF HOMOZYGOUS MUTANT CHIMERIC MICE - DELETION OF THE IMMUNOGLOBULIN HEAVY-CHAIN JOINING REGION BLOCKS B-CELL DEVELOPMENT AND ANTIBODY-PRODUCTION

被引:53
作者
JAKOBOVITS, A
VERGARA, GJ
KENNEDY, JL
HALES, JF
MCGUINNESS, RP
CASENTINIBOROCZ, DE
BRENNER, DG
OTTEN, GR
机构
[1] Cell Genesys, Inc., Foster City, CA 94404
关键词
B-CELL DEFICIENCY; IMMUNOGLOBULIN GENE REARRANGEMENT; GENE TARGETING; EMBRYONIC STEM CELLS;
D O I
10.1073/pnas.90.6.2551
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using a recently described method for efficiently deriving homozygous targeted alleles in embryonic stem cells, we produced chimeric mice whose tissues were derived partially from embryonic stem cells bearing homozygous deletion of the mouse immunoglobulin heavy-chain joining (J(H)) region. Characterization of these chimeric mice indicated that homozygous J(H) deletion leads to arrest of B-cell development at an early stage, resulting in a total lack of peripheral B cells and serum IgM. These results were confirmed in mice containing the homozygous J(H) deletion in their germ line. This novel B-cell-deficient mouse strain provides a tool for studying the recombination and expression of exogenous immunoglobulin genes introduced into the mouse germ line.
引用
收藏
页码:2551 / 2555
页数:5
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