Sullivan K F, Havercroft J C, Machlin P S, Cleveland D W
Mol Cell Biol. 1986 Dec;6(12):4409-18. doi: 10.1128/mcb.6.12.4409-4418.1986.
We have determined the nucleotide sequence of the chicken beta 5 (c beta 5)-tubulin gene. The gene displayed the coding structure common to all previously studied vertebrate beta-tubulin genes and was divided into four exon sequences interrupted by three intervening sequences (located between codons 19 and 20, within codon 56, and within codon 93). Comparison of the predicted polypeptide sequence encoded by c beta 5 with those of four other available chicken beta-tubulin sequences revealed that c beta 5 encoded a highly divergent beta-tubulin polypeptide isotype which was distinguished from previously known sequences primarily by two discrete variable sequence domains. However, c beta 5 uniquely shared identity in 16 residue positions with another divergent chicken beta-tubulin gene, c beta 4. These common sequences distinguished c beta 4 and c beta 5 from the remaining three chicken beta-tubulin genes. Analysis of the expression of c beta 5 and c beta 4 revealed a strikingly complementary pattern of gene expression: c beta 5 was expressed in a wide variety of cell and tissue types but not in neurons, whereas c beta 4 expression was detected uniquely in neuronal cells. Overall, these findings suggest the existence of two divergent families of beta-tubulin sequences in the chicken and further raise the possibility that the complementary expression of the c beta 4 and c beta 5 genes may fulfill a requirement for the presence of a divergent beta-tubulin polypeptide isotype in all cell types.
我们已经确定了鸡β5(cβ5)微管蛋白基因的核苷酸序列。该基因呈现出所有先前研究过的脊椎动物β微管蛋白基因共有的编码结构,被分为四个外显子序列,由三个间隔序列隔开(位于密码子19和20之间、密码子56内以及密码子93内)。将cβ5编码的预测多肽序列与其他四个可用的鸡β微管蛋白序列进行比较,发现cβ5编码了一种高度分化的β微管蛋白多肽亚型,其与先前已知序列的主要区别在于两个离散的可变序列结构域。然而,cβ5在16个残基位置上与另一个分化的鸡β微管蛋白基因cβ4具有独特的相同序列。这些共同序列将cβ4和cβ5与其余三个鸡β微管蛋白基因区分开来。对cβ5和cβ4表达的分析揭示了一种显著互补的基因表达模式:cβ5在多种细胞和组织类型中表达,但在神经元中不表达,而cβ4的表达仅在神经元细胞中检测到。总体而言,这些发现表明鸡中存在两个分化的β微管蛋白序列家族,并进一步增加了cβ4和cβ5基因的互补表达可能满足所有细胞类型中存在分化的β微管蛋白多肽亚型这一需求的可能性。