Eng F J, Warner J R
Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461.
Cell. 1991 May 31;65(5):797-804. doi: 10.1016/0092-8674(91)90387-e.
In S. cerevisiae, ribosomal protein L32 regulates the splicing of the transcript of its own gene, RPL32. We have identified an RNA structure within the transcript that is responsible for this regulation. Initial deletions limited essential sequences to the 5' exon and the first few nucleotides of the intron. To take advantage of phylogenetic comparison of RNA structures, RPL32 was cloned from the closely related species, Kluyveromyces lactis. The splicing of its transcript is similarly regulated. Sequences conserved between the S. cerevisiae and K. lactis transcripts suggested a structure involving base pairing of a region encompassing the 5' splice site with another near the 5' end of the transcript. Analysis of numerous site-directed mutations supports this structure. We infer that stabilization of this structure by L32 inhibits splicing by precluding the interaction of U1 RNA with the 5' splice site.
在酿酒酵母中,核糖体蛋白L32调节其自身基因RPL32转录本的剪接。我们在该转录本中鉴定出一个负责这种调节的RNA结构。最初的缺失将必需序列限制在5'外显子和内含子的前几个核苷酸。为了利用RNA结构的系统发育比较,从密切相关的乳酸克鲁维酵母物种中克隆了RPL32。其转录本的剪接受到类似的调节。酿酒酵母和乳酸克鲁维酵母转录本之间保守的序列提示了一种结构,该结构涉及包含5'剪接位点的区域与转录本5'端附近另一个区域的碱基配对。对大量定点突变的分析支持了这种结构。我们推断,L32对这种结构的稳定作用通过阻止U1 RNA与5'剪接位点的相互作用来抑制剪接。