Johnsen L B, Rasmussen L K, Petersen T E, Berglund L
Protein Chemistry Laboratory, University of Aarhus, Denmark.
Biochem J. 1995 Jul 1;309 ( Pt 1)(Pt 1):237-42. doi: 10.1042/bj3090237.
Here we report the molecular cloning and sequencing of three types of human alpha s1-casein transcripts and present evidence indicating that exon skipping is responsible for deleted mRNA transcripts. The largest transcript comprised 981 bp encoding a signal peptide of 15 amino acids followed by the mature alpha s1-casein sequence of 170 amino acids. Human alpha s1-casein has been reported to exist naturally as a multimer in complex with kappa-casein in mature human milk, thereby being unique among alpha s1-caseins [Rasmussen, Due and Petersen (1995) Comp. Biochem. Physiol., in the press]. The present demonstration of three cysteines in the mature protein provides a molecular explanation of the interactions in this complex. Tissue-specific expression of human alpha s1-casein was indicated by Northern-blot analysis. In addition, two cryptic exons were localized in the bovine alpha s1-casein gene.
在此,我们报告了三种类型的人αs1-酪蛋白转录本的分子克隆和测序,并提供证据表明外显子跳跃是缺失的mRNA转录本的原因。最大的转录本包含981 bp,编码一个15个氨基酸的信号肽,其后是170个氨基酸的成熟αs1-酪蛋白序列。据报道,人αs1-酪蛋白在成熟人乳中天然以与κ-酪蛋白复合的多聚体形式存在,因此在αs1-酪蛋白中是独特的[拉斯穆森、杜和彼得森(1995年)《比较生物化学与生理学》,即将出版]。成熟蛋白中三个半胱氨酸的目前证明为该复合物中的相互作用提供了分子解释。Northern印迹分析表明了人αs1-酪蛋白的组织特异性表达。此外,在牛αs1-酪蛋白基因中定位了两个隐蔽外显子。