Helfman D M, Ricci W M
Cold Spring Harbor Laboratory, NY 11724.
Nucleic Acids Res. 1989 Jul 25;17(14):5633-50. doi: 10.1093/nar/17.14.5633.
The rat tropomyosin 1 gene gives rise to two mRNAs encoding rat fibroblast TM-1 and skeletal muscle beta-tropomyosin via an alternative splicing mechanism. The gene is comprised of 11 exons. Exons 1 through 5 and exons 8 and 9 are common to all mRNAs expressed from this gene. Exons 6 and 11 are used in fibroblasts as well as smooth muscle whereas exons 7 and 10 are used exclusively in skeletal muscle. In the present studies we have focused on the mutually exclusive internal alternative splice choice involving exon 6 (fibroblast-type splice) and exon 7 (skeletal muscle-type splice). To study the mechanism and regulation of alternative splice site selection we have characterized the branch points used in processing of the tropomyosin pre-mRNAs in vitro using nuclear extracts obtained from HeLa cells. Splicing of exon 5 to exon 6 (fibroblast-type splice) involves the use of three branch points located 25, 29, and 36 nucleotides upstream of the 3' splice site of exon 6. Splicing of exon 6 (fibroblast-type splice) or exon 7 (skeletal muscle type-splice) to exon 8 involves the use of the same branch point located 24 nucleotides upstream of this shared 3' splice site. In contrast, the splicing of exon 5 to exon 7 (skeletal muscle-type splice) involves the use of three branch sites located 144, 147 and 153 nucleotides, upstream of the 3' splice site of exon 7. In addition, the pyrimidine content of the region between these unusual branch points and the 3' splice site of exon 7 was found to be greater than 80%. These studies raise the possibility that the use of branch points located a long distance from a 3' splice site may be an essential feature of some alternatively spliced exons. The possible significance of these unusual branch points as well as a role for the polypyrimidine stretch in intron 6 in splice site selection are discussed.
大鼠原肌球蛋白1基因通过可变剪接机制产生两种mRNA,分别编码大鼠成纤维细胞TM-1和骨骼肌β-原肌球蛋白。该基因由11个外显子组成。外显子1至5以及外显子8和9是该基因表达的所有mRNA所共有的。外显子6和11用于成纤维细胞和平滑肌,而外显子7和10仅用于骨骼肌。在本研究中,我们重点关注了涉及外显子6(成纤维细胞型剪接)和外显子7(骨骼肌型剪接)的互斥性内部可变剪接选择。为了研究可变剪接位点选择的机制和调控,我们使用从HeLa细胞获得的核提取物,对体外原肌球蛋白前体mRNA加工过程中使用的分支点进行了表征。外显子5与外显子6的剪接(成纤维细胞型剪接)涉及使用位于外显子6的3'剪接位点上游25、29和36个核苷酸处的三个分支点。外显子6(成纤维细胞型剪接)或外显子7(骨骼肌型剪接)与外显子8的剪接涉及使用位于这个共享的3'剪接位点上游24个核苷酸处的同一个分支点。相比之下,外显子5与外显子7的剪接(骨骼肌型剪接)涉及使用位于外显子7的3'剪接位点上游144、147和153个核苷酸处的三个分支位点。此外,发现这些异常分支点与外显子7的3'剪接位点之间区域的嘧啶含量大于80%。这些研究提出了一种可能性,即使用距离3'剪接位点较远的分支点可能是一些可变剪接外显子的一个基本特征。讨论了这些异常分支点的可能意义以及内含子6中的多嘧啶序列在剪接位点选择中的作用。