Engler P, Haasch D, Pinkert C A, Doglio L, Glymour M, Brinster R, Storb U
Department of Molecular Genetics and Cell Biology, University of Chicago.
Cell. 1991 Jun 14;65(6):939-47. doi: 10.1016/0092-8674(91)90546-b.
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.
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。