Porter G, Brennwald P, Wise J A
Department of Biochemistry, University of Illinois, Urbana 61801.
Mol Cell Biol. 1990 Jun;10(6):2874-81. doi: 10.1128/mcb.10.6.2874-2881.1990.
We have cloned, sequenced, and disrupted the gene encoding U1 small nuclear RNA (snRNA) in the fission yeast Schizosaccharomyces pombe. This RNA is close in size and exhibits a high degree of secondary structure homology to human U1 RNA. There exist two regions of extended primary sequence identity between S. pombe and human U1 RNAs; the first comprises nucleotides involved in hydrogen bonding to 5' splice junctions, and the second is a single-stranded region which, in the human snRNA, forms part of the A protein binding site. S. pombe U1 lacks two nucleotides just following the 5' cap structure which are present in all other U1 homologs examined to date, and the region which corresponds to the binding site for the human 70K protein (molecular weight of 55,000) is more divergent than in other organisms. A putative upstream transcription signal is conserved in sequence and location among all loci encoding spliceosomal snRNAs in S. pombe with the exception of U6. Disruption of the single-copy U1 gene, designated snu1, reveals that this RNA is indispensable for viability.
我们已经克隆、测序并破坏了裂殖酵母粟酒裂殖酵母中编码U1小核RNA(snRNA)的基因。这种RNA在大小上相近,并且与人类U1 RNA在二级结构上具有高度同源性。粟酒裂殖酵母和人类U1 RNA之间存在两个延伸的一级序列相同区域;第一个区域包含与5'剪接接头形成氢键的核苷酸,第二个区域是一个单链区域,在人类snRNA中,它构成A蛋白结合位点的一部分。粟酒裂殖酵母U1在5'帽结构之后缺少两个核苷酸,而这两个核苷酸在迄今为止检测的所有其他U1同源物中都存在,并且与人类70K蛋白(分子量为55,000)结合位点相对应的区域比其他生物体中的差异更大。除U6外,在粟酒裂殖酵母中所有编码剪接体snRNA的基因座中,一个推定的上游转录信号在序列和位置上都是保守的。破坏单拷贝的U1基因(命名为snu1)表明,这种RNA对于细胞存活是必不可少的。