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鸡原肌球蛋白1基因通过可变剪接产生9种mRNA。

The chicken tropomyosin 1 gene generates nine mRNAs by alternative splicing.

作者信息

Forry-Schaudies S, Hughes S H

机构信息

ABL-Basic Research Program, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201.

出版信息

J Biol Chem. 1991 Jul 25;266(21):13821-7.

PMID:1856215
Abstract

Skeletal muscle beta-tropomyosin, smooth muscle alpha-tropomyosin, and a low molecular weight fibroblast tropomyosin are generated by alternatively splicing RNA transcripts of the chicken tropomyosin 1 (TM 1) gene (Forry-Schaudies, S., Maihle, N. J., and Hughes, S. H. (1990) J. Mol. Biol. 211; 321-330). Two novel tropomyosin cDNAs that derive from mRNAs of the TM 1 gene have been isolated from a chicken embryo brain cDNA library. Brain cDNA BRT-1 is 2.2 kilobases in length and encodes 283 amino acids. It is identical to skeletal muscle beta-tropomyosin from amino acids 1 to 258. The sequence 3' of this point is unique to BRT-1; a comparison to genomic sequence indicates that a new carboxyl-terminal exon is used to generate this sequence. 1.4-kilobase brain cDNA BRT-2 contains sequences found in both fibroblast cDNA FT-beta (5'-end) and skeletal muscle cDNA SKT-beta (3'-end). RNase and S1 nuclease assays using RNA samples from leg muscle, gizzard, fibroblasts, and brain indicate that the TM 1 gene expresses four additional tropomyosin RNAs by alternately splicing previously characterized exons. These results demonstrate that the chicken TM 1 gene encodes nine tropomyosin RNAs through the use of two promoters, two internal exons that are mutually exclusive, and three 3'-exons. Implications for the regulation of alternative splicing are discussed.

摘要

骨骼肌β-原肌球蛋白、平滑肌α-原肌球蛋白和一种低分子量成纤维细胞原肌球蛋白是由鸡原肌球蛋白1(TM 1)基因的RNA转录本选择性剪接产生的(福里-绍迪斯,S.,迈勒,N. J.,和休斯,S. H.(1990年)《分子生物学杂志》211;321 - 330)。从鸡胚脑cDNA文库中分离出了两个源自TM 1基因mRNA的新型原肌球蛋白cDNA。脑cDNA BRT - 1长度为2.2千碱基,编码283个氨基酸。从氨基酸1到258它与骨骼肌β-原肌球蛋白相同。该位点3'端的序列是BRT - 1特有的;与基因组序列比较表明,一个新的羧基末端外显子用于产生该序列。1.4千碱基的脑cDNA BRT - 2包含在成纤维细胞cDNA FT-β(5'端)和骨骼肌cDNA SKT-β(3'端)中都发现的序列。使用来自腿部肌肉、砂囊、成纤维细胞和脑的RNA样本进行的核糖核酸酶和S1核酸酶分析表明,TM 1基因通过选择性剪接先前已鉴定的外显子表达另外四种原肌球蛋白RNA。这些结果表明,鸡TM 1基因通过使用两个启动子、两个相互排斥的内部外显子和三个3'端外显子编码九种原肌球蛋白RNA。讨论了对选择性剪接调控的影响。

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