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杜氏利什曼原虫分化过程中β-微管蛋白合成的翻译控制证据。

Evidence for translational control of beta-tubulin synthesis during differentiation of Leishmania donovani.

作者信息

Bhaumik M, Das S, Adhya S

机构信息

Genetic Engineering Laboratory, Indian Institute of Chemical Biology, Calcutta.

出版信息

Parasitology. 1991 Oct;103 Pt 2:197-205. doi: 10.1017/s0031182000059485.

Abstract

Tubulin biosynthesis was rapidly induced during transformation of the mammalian (amastigote) stage of the kinetoplastid parasite Leishmania donovani to flagellated promastigotes. However, transcription of beta-tubulin genes occurred constitutively, as judged by nascent RNA synthesis in isolated nuclei and Northern blotting of steady-state mRNA. Two mRNA species of 2.2 and 2.4 kb were shared by the two cell-types, while a third 2.6 kb species, constituting about 20% of the total, was present in large amounts in promastigotes. RNase protection experiments demonstrated sequence microheterogeneity in the 5'-untranslated region, the pattern of which was identical in promastigotes and amastigotes. By primer extension assays, heterogeneity in the 5'-terminal cap structure of amastigote beta-tubulin mRNA and differential pausing of reverse transcriptase within the mini-exon leader region were detected. These differences correlated with enhanced translational efficiency of tubulin mRNA from promastigotes in a rabbit reticulocyte lysate system. The results indicate that translational control plays a major role in tubulin induction during L. donovani differentiation.

摘要

在动基体寄生虫杜氏利什曼原虫的哺乳动物(无鞭毛体)阶段转化为有鞭毛的前鞭毛体的过程中,微管蛋白生物合成迅速被诱导。然而,通过分离细胞核中的新生RNA合成以及稳态mRNA的Northern印迹分析判断,β-微管蛋白基因的转录是组成性的。两种细胞类型共有2.2 kb和2.4 kb的两种mRNA,而第三种2.6 kb的mRNA(约占总量的20%)在前鞭毛体中大量存在。核糖核酸酶保护实验证明了5'-非翻译区的序列微异质性,其模式在前鞭毛体和无鞭毛体中是相同的。通过引物延伸分析,检测到无鞭毛体β-微管蛋白mRNA的5'-末端帽结构的异质性以及逆转录酶在小外显子前导区内的差异停顿。这些差异与前鞭毛体微管蛋白mRNA在兔网织红细胞裂解物系统中翻译效率的提高相关。结果表明,翻译控制在杜氏利什曼原虫分化过程中的微管蛋白诱导中起主要作用。

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