Soriano P, Gridley T, Jaenisch R
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
Genes Dev. 1987 Jun;1(4):366-75. doi: 10.1101/gad.1.4.366.
Thirty-four transgenic mouse strains, each carrying a single proviral insert, were generated by infection of preimplantation and postimplantation embryos with retroviruses. Animals homozygous for proviral integrations were derived for all strains with the exception of Mov 24, where the provirus is inserted on the Y chromosome, and Mov 34. Embryos homozygous at the Mov 34 locus develop normally to the blastocyst stage and die shortly after implantation, indicating that virus integration resulted in a recessive lethal mutation. The provirus and flanking sequences were cloned and the virus was mapped to the 5' side of an abundantly and ubiquitously transcribed gene. Similar to the previously derived Mov 13 mutation, proviral integration at the Mov 34 locus interferes with the expression of the adjacent gene. These and our previous results indicate that of a total of 48 proviral integrations in the germ line, two resulted in transgenic mouse strains with recessive lethal mutations.
通过用逆转录病毒感染植入前和植入后的胚胎,产生了34种转基因小鼠品系,每个品系携带一个单一的前病毒插入片段。除了Mov 24(其前病毒插入在Y染色体上)和Mov 34外,所有品系都获得了前病毒整合的纯合动物。在Mov 34位点纯合的胚胎正常发育到囊胚阶段,并在植入后不久死亡,这表明病毒整合导致了隐性致死突变。克隆了前病毒和侧翼序列,并将该病毒定位到一个大量且普遍转录的基因的5'端。与先前获得的Mov 13突变相似,Mov 34位点的前病毒整合干扰了相邻基因的表达。这些以及我们之前的结果表明,在生殖系中总共48次前病毒整合中,有两次导致了具有隐性致死突变的转基因小鼠品系。