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将人类γ1免疫球蛋白基因导入受精的小鼠卵中。

Introduction of human gamma 1 immunoglobulin genes into fertilized mouse eggs.

作者信息

Yamamura K, Kikutani H, Takahashi N, Taga T, Akira S, Kawai K, Fukuchi K, Kumahara Y, Honjo T, Kishimoto T

出版信息

J Biochem. 1984 Aug;96(2):357-63. doi: 10.1093/oxfordjournals.jbchem.a134845.

Abstract

A rearranged human gamma 1 immunoglobulin gene was introduced into fertilized mouse eggs. The phage Ch4A-VCE-gamma 1 was constructed by ligating an EcoRI and BglII fragment of pBR322-CESSV(CE-1) containing the VDJ region with an EcoRI and BamHI fragment of Ch4A-HIg gamma 1-10 containing the gamma 1 constant region. About 200 copies of Ch4A-VCE-gamma 1 genes were introduced into fertilized mouse eggs. Of 489 eggs injected with these genes, 319 survived and were transferred to oviducts of foster mothers. Thirtyeight mice were born and were screened for the presence of human gamma 1 immunoglobulin genes by Southern blot hybridization. Five of these 38 mice had integrated human gamma 1 immunoglobulin genes. None of the human gamma 1 copies in each mouse had undergone deletions or rearrangements as judged by the Southern blotting patterns for several restriction enzymes. Human gamma 1 gene was present in several different tissues. All the mice tested so far transmit the human gamma 1 gene to a fraction of their offspring in an autosomal dominant manner. Spleen cells from transgenic mice were analyzed for immunoglobulin production by reverse plaque assay or immunofluorescence staining of cytoplasmic immunoglobulin, but synthesis and secretion of human gamma 1 chains could not be detected. No human gamma 1 immunoglobulin mRNA was detected in the liver and spleen of a transgenic mouse. The presence of the human gamma 1 immunoglobulin gene appeared to have no effect on the expression of endogenous mouse immunoglobulin genes.

摘要

将一个重排的人γ1免疫球蛋白基因导入受精的小鼠卵中。噬菌体Ch4A-VCE-γ1是通过将含有VDJ区域的pBR322-CESSV(CE-1)的EcoRI和BglII片段与含有γ1恒定区的Ch4A-HIgγ1-10的EcoRI和BamHI片段连接而构建的。将约200个Ch4A-VCE-γ1基因拷贝导入受精的小鼠卵中。在注射了这些基因的489个卵中,319个存活并被转移到代孕母亲的输卵管中。38只小鼠出生,并通过Southern印迹杂交筛选人γ1免疫球蛋白基因的存在。这38只小鼠中有5只整合了人γ1免疫球蛋白基因。根据几种限制性酶的Southern印迹图谱判断,每只小鼠中的人γ1拷贝均未发生缺失或重排。人γ1基因存在于几种不同的组织中。到目前为止,所有测试的小鼠都以常染色体显性方式将人γ1基因传递给一部分后代。通过反向空斑试验或细胞质免疫球蛋白的免疫荧光染色分析转基因小鼠脾细胞的免疫球蛋白产生情况,但未检测到人γ1链的合成和分泌。在转基因小鼠的肝脏和脾脏中未检测到人γ1免疫球蛋白mRNA。人γ1免疫球蛋白基因的存在似乎对内源小鼠免疫球蛋白基因的表达没有影响。

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