Frankel W N, Potter T A, Rajan T V
Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.
J Virol. 1989 Jun;63(6):2623-8. doi: 10.1128/JVI.63.6.2623-2628.1989.
We describe three B2mb mutants caused by integration of retroviral proviruses into the B2m gene. All three insertions occurred within 500 base pairs of each other in the 5' end of the first intron of the B2mb gene. Mutant cell line i1 contained a nonfunctional Abelson murine leukemia virus-initiated transcript that spliced into B2mb exon II; mutant cell lines i7 and i18 contained transcripts complementary to B2mb exon 1. Both i1 and i7 also contained small amounts of wild-type B2mb transcript. The implications of these studies for the development of retroviral insertional mutagenesis as a strategy for cloning previously uncloned genes are discussed.
我们描述了三种由逆转录病毒前病毒整合到B2m基因中引起的B2mb突变体。所有这三种插入都发生在B2mb基因第一个内含子5'端彼此相距500个碱基对的范围内。突变细胞系i1含有一个无功能的由阿贝尔逊鼠白血病病毒起始的转录本,该转录本剪接到B2mb外显子II中;突变细胞系i7和i18含有与B2mb外显子1互补的转录本。i1和i7还都含有少量野生型B2mb转录本。本文讨论了这些研究对于将逆转录病毒插入诱变作为克隆先前未克隆基因的策略的发展所具有的意义。