Burgoyne R D, Cambray-Deakin M A, Lewis S A, Sarkar S, Cowan N J
Physiological Laboratory, University of Liverpool, UK.
EMBO J. 1988 Aug;7(8):2311-9. doi: 10.1002/j.1460-2075.1988.tb03074.x.
We describe the structure and expression of a mammalian beta-tubulin isotype (M beta 6) that is weakly expressed in testis but is abundant in developing brain, with transcripts declining to lower levels in the adult brain. The expression of M beta 6 was undetectable in any other mouse tissue examined. A serum specific for this isotype was prepared using a cloned fusion protein as immunogen. M beta 6 is one of five known beta-tubulin isotypes expressed in brain, and using the anti-M beta 6 serum along with sera, anti-M beta 2, anti-M beta 3/4 and anti-M beta 5, previously characterized, we have examined the pattern of expression of beta-tubulin isotypes in rat cerebellum. The isotypes each have characteristic cell-type specific patterns of localization in cerebellum. M beta 2, M beta 3/4 and M beta 5 are present in both neuronal and non-neuronal cells, but in contrast M beta 6 was only detectable in neurons in tissue sections and in dissociated cerebellar cell culture. The majority of sequence differences among the beta-tubulin isotypes lie at the carboxy terminus, the region of beta-tubulin involved in MAP binding. In the case of M beta 2 and M beta 6, the patterns of expression are similar or identical to the patterns of expression of MAP3 and MAP1A respectively. These results suggest that beta-tubulin isotypes may contribute to the determination of the specific association of MAPs with microtubules of diverse function. However, the strict subcellular segregation of other MAPs in brain may be determined by other factors.
我们描述了一种哺乳动物β-微管蛋白亚型(Mβ6)的结构和表达情况。该亚型在睾丸中表达较弱,但在发育中的大脑中大量表达,其转录本在成年大脑中降至较低水平。在检测的任何其他小鼠组织中均未检测到Mβ6的表达。使用克隆的融合蛋白作为免疫原制备了针对该亚型的特异性血清。Mβ6是大脑中表达的五种已知β-微管蛋白亚型之一,利用抗Mβ6血清以及先前鉴定的抗Mβ2、抗Mβ3/4和抗Mβ5血清,我们研究了大鼠小脑β-微管蛋白亚型的表达模式。这些亚型在小脑中各自具有特征性的细胞类型特异性定位模式。Mβ2、Mβ3/4和Mβ5存在于神经元和非神经元细胞中,但相比之下,Mβ6仅在组织切片中的神经元以及解离的小脑细胞培养物中可检测到。β-微管蛋白亚型之间的大多数序列差异位于羧基末端,即β-微管蛋白中与微管相关蛋白(MAP)结合的区域。就Mβ2和Mβ6而言,其表达模式分别与MAP3和MAP1A的表达模式相似或相同。这些结果表明,β-微管蛋白亚型可能有助于确定MAP与具有不同功能的微管的特异性结合。然而,大脑中其他MAP的严格亚细胞分隔可能由其他因素决定。