Watanabe-Nagasu N, Itoh Y, Tani T, Okano K, Koga N, Okada N, Ohshima Y
Nucleic Acids Res. 1983 Mar 25;11(6):1791-801. doi: 10.1093/nar/11.6.1791.
Four phage clones which hybridize with U1 small nuclear RNA were obtained from a rat gene library. Two clones contain a presumed pseudogene. A third clone includes two gene candidates that are co-linear with the rat U1-RNA, 3.6kb apart and in the opposite orientation. The two genes are surrounded by identical sequences of 491bp upstream and 178bp downstream. The upstream sequences do not contain a TATA box, but share many block homologies with those for the human U1-RNA gene(1-3). A 101bp "identifier (ID) sequence", which was reported to be specifically expressed in rat brain (4), is inserted immediately after the shared sequence downstream of one of the genes. In the fourth clone, there are two putative pseudogenes, which have one or three nucleotide changes, 3kb apart and in the same orientation. Southern blot analysis of total rat DNA reveals about 50 U1-RNA genes/pseudogenes in the genome.
从大鼠基因文库中获得了四个与U1小核RNA杂交的噬菌体克隆。两个克隆包含一个推测的假基因。第三个克隆包含两个候选基因,它们与大鼠U1-RNA共线,相距3.6kb且方向相反。这两个基因被上游491bp和下游178bp的相同序列所包围。上游序列不含TATA盒,但与人类U1-RNA基因的上游序列有许多区域同源性(1-3)。一个101bp的“识别(ID)序列”,据报道在大鼠脑中特异性表达(4),在其中一个基因下游的共享序列之后立即插入。在第四个克隆中,有两个推定的假基因,它们有一个或三个核苷酸变化,相距3kb且方向相同。大鼠总DNA的Southern印迹分析显示基因组中约有50个U1-RNA基因/假基因。