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携带突变型人类IgM基因的转基因小鼠中的等位基因排斥。

Allelic exclusion in transgenic mice carrying mutant human IgM genes.

作者信息

Nussenzweig M C, Shaw A C, Sinn E, Campos-Torres J, Leder P

机构信息

Howard Hughes Medical Institute, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Exp Med. 1988 Jun 1;167(6):1969-74. doi: 10.1084/jem.167.6.1969.

Abstract

Expression of the membrane-bound version of the human mu chain in transgenic mice results in the allelic exclusion of endogenous mouse Ig heavy chain genes (6). The secreted version of the human Ig transgene has no such effect. F1 hybrid animals that carry transgenes for both secreted and membrane-bound human mu chains produce both forms of the human heavy chain while strongly suppressing endogenous mouse mu expression. The simultaneous expression of the two rearranged transgenes in primary B cells suggests that allelic exclusion operates before the formation of a second functionally rearranged heavy chain gene in vivo.

摘要

在转基因小鼠中表达人μ链的膜结合形式会导致内源性小鼠Ig重链基因的等位基因排斥(6)。人Ig转基因的分泌形式则没有这种作用。携带分泌型和膜结合型人μ链转基因的F1杂交动物会产生两种形式的人重链,同时强烈抑制内源性小鼠μ链的表达。两种重排转基因在原代B细胞中的同时表达表明,等位基因排斥在体内第二个功能性重排重链基因形成之前就起作用了。

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