Villasante A, Wang D, Dobner P, Dolph P, Lewis S A, Cowan N J
Mol Cell Biol. 1986 Jul;6(7):2409-19. doi: 10.1128/mcb.6.7.2409-2419.1986.
Five mouse alpha-tubulin isotypes are described, each distinguished by the presence of unique amino acid substitutions within the coding region. Most, though not all of these isotype-specific amino acids, are clustered at the carboxy terminus. One of the alpha-tubulin isotypes described is expressed exclusively in testis and is encoded by two closely related genes (M alpha 3 and M alpha 7) which have homologous 3' untranslated regions but which differ at multiple third codon positions and in their 5' untranslated regions. We show that a subfamily of alpha-tubulin genes encoding the same testis-specific isotype also exists in humans. Thus, we conclude that the duplication event leading to a pair of genes encoding a testis-specific alpha-tubulin isotype predated the mammalian radiation, and both members of the duplicated sequence have been maintained since species divergence. A second alpha-tubulin gene, M alpha 6, is expressed ubiquitously at a low level, whereas a third gene, M alpha 4, is unique in that it does not encode a carboxy-terminal tyrosine residue. This gene yields two transcripts: a 1.8-kilobase (kb) mRNA that is abundant in muscle and a 2.4-kb mRNA that is abundant in testis. Whereas the 1.8-kb mRNA encodes a distinct alpha-tubulin isotype, the 2.4-kb mRNA is defective in that the methionine residue required for translational initiation is missing. Patterns of developmental expression of the various alpha-tubulin isotypes are presented. Our data support the view that individual tubulin isotypes are capable of conferring functional specificity on different kinds of microtubules.
已描述了五种小鼠α-微管蛋白同种型,每种同种型在编码区内存在独特的氨基酸取代,以此相互区分。这些同种型特异性氨基酸中的大多数(并非全部)聚集在羧基末端。所描述的一种α-微管蛋白同种型仅在睾丸中表达,由两个密切相关的基因(Mα3和Mα7)编码,这两个基因具有同源的3'非翻译区,但在多个第三位密码子位置以及5'非翻译区存在差异。我们发现人类中也存在一个编码相同睾丸特异性同种型的α-微管蛋白基因亚家族。因此,我们得出结论,导致一对编码睾丸特异性α-微管蛋白同种型的基因的复制事件发生在哺乳动物辐射之前,并且自物种分化以来,复制序列的两个成员都得以保留。第二个α-微管蛋白基因Mα6在全身低水平表达,而第三个基因Mα4的独特之处在于它不编码羧基末端酪氨酸残基。该基因产生两种转录本:一种1.8千碱基(kb)的mRNA在肌肉中丰富,另一种2.4 kb的mRNA在睾丸中丰富。虽然1.8 kb的mRNA编码一种独特的α-微管蛋白同种型,但2.4 kb的mRNA存在缺陷,因为缺少翻译起始所需的甲硫氨酸残基。本文展示了各种α-微管蛋白同种型的发育表达模式。我们的数据支持这样一种观点,即单个微管蛋白同种型能够赋予不同类型微管功能特异性。