Bond J F, Robinson G S, Farmer S R
Mol Cell Biol. 1984 Jul;4(7):1313-9. doi: 10.1128/mcb.4.7.1313-1319.1984.
We recently demonstrated that beta-tubulin mRNA expression is regulated during rat brain development. This is manifested by a dramatic decrease in both 1.8- and 2.9-kilobase (kb) mRNAs when extensive neurite elongation is occurring. Coincident with these decreases is the increased production of a 2.5-kb mRNA. (J.F. Bond and S.R. Farmer, Mol. Cell. Biol. 3:1333-1342, 1983). In the present study, we have isolated and characterized three different cDNAs corresponding to beta-tubulin mRNAs (R beta T.1, R beta T.2, and R beta T.3). Hybridization of 3' untranslated region subclones of R beta T.1 and R beta T.2 cDNAs to RNA from a variety of rat tissues and cells revealed that these two cDNAs are neural cell specific. R beta T.1 corresponds to an abundant 1.8-kb mRNA expressed only at early stages of rat brain development. R beta T.2 corresponds to the 2.5-kb mRNA expressed at later stages. These data strongly suggest that there is differential expression of the beta-tubulin multigene family during rat brain development.
我们最近证明,β-微管蛋白mRNA的表达在大鼠脑发育过程中受到调控。这表现为在广泛的神经突伸长发生时,1.8千碱基(kb)和2.9千碱基的mRNA均显著减少。与这些减少同时发生的是2.5千碱基mRNA产量的增加。(J.F.邦德和S.R.法默,《分子与细胞生物学》3:1333 - 1342,1983年)。在本研究中,我们分离并鉴定了三种与β-微管蛋白mRNA相对应的不同cDNA(RβT.1、RβT.2和RβT.3)。RβT.1和RβT.2 cDNA的3'非翻译区亚克隆与来自多种大鼠组织和细胞的RNA杂交显示,这两种cDNA是神经细胞特异性的。RβT.1对应于仅在大鼠脑发育早期表达的丰富的1.8千碱基mRNA。RβT.2对应于在后期表达的2.5千碱基mRNA。这些数据强烈表明,在大鼠脑发育过程中β-微管蛋白多基因家族存在差异表达。