Muth K, Bruyns R, Thorey I S, von Melchner H
Department of Hematology, University of Frankfurt Medical School, Germany.
Dev Dyn. 1998 Jun;212(2):277-83. doi: 10.1002/(SICI)1097-0177(199806)212:2<277::AID-AJA12>3.0.CO;2-1.
A retroviral gene trap vector (U3Tkneo) that selects for integrations in or near expressed 5' exons has been used to identify genes that are repressed during hematopoietic differentiation of mouse totipotent embryonic stem cells. The vector contains coding sequences for an HSV-thymidine kinase/neomycin phosphotransferase fusion protein in the U3 region of a Moloney murine leukemia virus LTR and allows selection for (G418) and against (Ganciclovir; GC) U3 gene expression. A total of 208 neomycin-resistant clones were isolated following infection with U3tkneo and screened for integrations into regulated genes by using a two-step, semisolid culture system that supports hematopoietic differentiation. Two clones contained U3Tkneo integrations in genes that were repressed selectively in hematopoietic cells. Analysis of upstream proviral flanking sequences indicated that both integrations occurred into unknown genes. One up-stream sequence identified a cellular transcript that was expressed differentially in the kidneys and liver of adult mice. When this fusion gene was passaged to the germ line, homozygous offspring with nearly null mutations were obtained. However, mutant mice were normal, suggesting that potential loss of function phenotypes are subtle and may be restricted to the kidneys and the liver.
一种逆转录病毒基因捕获载体(U3Tkneo)可用于选择在表达的5'外显子内或附近的整合,已被用于鉴定在小鼠全能胚胎干细胞造血分化过程中被抑制的基因。该载体在莫洛尼鼠白血病病毒LTR的U3区域包含单纯疱疹病毒胸苷激酶/新霉素磷酸转移酶融合蛋白的编码序列,并允许对U3基因表达进行正向选择(G418)和反向选择(更昔洛韦;GC)。用U3tkneo感染后共分离出208个新霉素抗性克隆,并通过使用支持造血分化的两步半固体培养系统筛选整合到调控基因中的克隆。两个克隆在造血细胞中被选择性抑制的基因中含有U3Tkneo整合。对上游前病毒侧翼序列的分析表明,两种整合均发生在未知基因中。一个上游序列鉴定出一种在成年小鼠肾脏和肝脏中差异表达的细胞转录本。当这个融合基因传递到种系时,获得了几乎无突变的纯合后代。然而,突变小鼠是正常的,这表明潜在的功能丧失表型很细微,可能仅限于肾脏和肝脏。