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小鼠4号染色体上的一个品系特异性修饰因子控制着独立转基因位点的甲基化。

A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci.

作者信息

Engler P, Haasch D, Pinkert C A, Doglio L, Glymour M, Brinster R, Storb U

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago.

出版信息

Cell. 1991 Jun 14;65(6):939-47. doi: 10.1016/0092-8674(91)90546-b.

Abstract

A transgene, pHRD, is highly methylated in 12 independent mouse lines when in a C57BL/6 strain background, but becomes progressively less methylated when bred into a DBA/2 background. Transgenes inherited from the mother are generally more methylated; however, this parental effect disappears following continued breeding into the nonmethylating strain. Mapping experiments using BXD recombinant inbred mice as well as other inbred strains indicate that a single strain-specific modifier (Ssm-1) linked to, but distinct from, Fv-1 is responsible for the strain effect. In addition to the methylated and unmethylated transgenic phenotypes, certain mice exhibit a partial methylation pattern that is a consequence of an unusual cellular mosaicism. The pHRD transgene, containing target sequences for the V(D)J recombinase, undergoes site-specific recombination only in lymphoid tissues. This V-J joining is restricted primarily to unmethylated transgene copies.

摘要

转基因pHRD在C57BL/6品系背景下的12个独立小鼠品系中高度甲基化,但在培育到DBA/2背景中时甲基化程度逐渐降低。从母亲遗传的转基因通常甲基化程度更高;然而,在持续培育到非甲基化品系后,这种亲本效应消失。使用BXD重组近交系小鼠以及其他近交系进行的定位实验表明,与Fv-1连锁但不同的单个品系特异性修饰因子(Ssm-1)负责这种品系效应。除了甲基化和未甲基化的转基因表型外,某些小鼠表现出部分甲基化模式,这是一种不寻常的细胞镶嵌现象的结果。含有V(D)J重组酶靶序列的pHRD转基因仅在淋巴组织中发生位点特异性重组。这种V-J连接主要限于未甲基化的转基因拷贝。

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