Goldring A, Michaeli S
Department of Membrane Research and Biophysics, Weizmann Institute of Science, Rehovot, Israel.
Gene. 1995 Apr 14;156(1):139-44. doi: 10.1016/0378-1119(95)00048-b.
The U6 snRNA (U6) is the most conserved small nuclear RNA (snRNA) and apparently plays a central role in catalysis of the cis-splicing reaction. In trans-splicing, U6 may have an additional function. In the nematode trans-splicing system, a direct interaction between the U6 and spliced leader (SL) RNAs has been demonstrated, suggesting that U6 may serve as a bridge between the SL RNA and the acceptor pre-mRNA. To examine possible phylogenetic conservation of trypanosomatid U6 sequences that may interact with spliceosomal RNAs, we have cloned and sequenced the U6 gene from the monogenetic trypanosomatid Leptomonas collosoma (Lc). The Lc U6 deviates from the Trypanosoma brucei (Tb) RNA only in four positions located in the 5' stem-loop and the central domains. As in Tb, U6 is a single-copy gene and two tRNA genes, tRNAGln and tRNAIle, are found upstream to the gene. The tRNAs are differentially expressed; tRNAGln is transcribed in the opposite direction to U6, whereas tRNAIle is not transcribed. Possible base-pairing between U6 and the U2 and SL RNAs, similar to the interactions that take place in the nematode trans-splicing system, are proposed.
U6小核RNA(U6)是最保守的小核RNA(snRNA),显然在顺式剪接反应的催化中起核心作用。在反式剪接中,U6可能具有额外的功能。在线虫反式剪接系统中,已证实U6与剪接前导(SL)RNA之间存在直接相互作用,这表明U6可能作为SL RNA与受体前体mRNA之间的桥梁。为了研究可能与剪接体RNA相互作用的锥虫U6序列的系统发育保守性,我们从单基因锥虫粗线细滴虫(Lc)中克隆并测序了U6基因。Lc U6与布氏锥虫(Tb)RNA仅在位于5'茎环和中央结构域的四个位置存在差异。与Tb一样,U6是单拷贝基因,并且在该基因上游发现了两个tRNA基因,即tRNAGln和tRNAIle。这些tRNA的表达存在差异;tRNAGln与U6的转录方向相反,而tRNAIle不转录。有人提出,U6与U2和SL RNA之间可能存在碱基配对,类似于线虫反式剪接系统中发生的相互作用。