Weaver D, Costantini F, Imanishi-Kari T, Baltimore D
Cell. 1985 Aug;42(1):117-27. doi: 10.1016/s0092-8674(85)80107-0.
Transgenic mice containing a microinjected rearranged immunoglobulin (Ig) mu heavy chain gene were examined for the effects on DNA rearrangement of the endogenous Ig genes. Abelson murine leukemia virus (A-MuLV) cell lines were isolated from pre-B cells of transgenic mice and of normal littermates. Microinjected mu gene RNA and a mu heavy chain protein were synthesized in every transgenic A-MuLV cell line. Only 10% of normal mouse A-MuLV transformants synthesized mu protein. A germ-line JH allele was observed in 40% of the transgenic lines, demonstrating that the block to endogenous Ig DNA rearrangement occurred at the first step of heavy chain DNA joining. All alleles were rearranged in normal mouse A-MuLV lines. Germline JH alleles were also detected in 10% of the transgenic hybridomas derived from proliferating B cells. Our results support a model of active prevention of rearrangement by the product of successfully rearranged mu genes.
对含有显微注射重排免疫球蛋白(Ig)μ重链基因的转基因小鼠进行了检测,以研究其对内源Ig基因DNA重排的影响。从转基因小鼠和正常同窝小鼠的前B细胞中分离出阿贝尔森鼠白血病病毒(A-MuLV)细胞系。在每个转基因A-MuLV细胞系中均合成了显微注射的μ基因RNA和μ重链蛋白。只有10%的正常小鼠A-MuLV转化体合成μ蛋白。在40%的转基因系中观察到种系JH等位基因,表明对内源Ig DNA重排的阻断发生在重链DNA连接的第一步。在正常小鼠A-MuLV系中所有等位基因均发生了重排。在10%源自增殖B细胞的转基因杂交瘤中也检测到种系JH等位基因。我们的结果支持一个由成功重排的μ基因产物主动预防重排的模型。