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构巢曲霉中条件致死性微管蛋白Aα-微管蛋白突变

Conditionally lethal tubA alpha-tubulin mutations in Aspergillus nidulans.

作者信息

Oakley B R, Oakley C E, Rinehart J E

出版信息

Mol Gen Genet. 1987 Jun;208(1-2):135-44. doi: 10.1007/BF00330434.

Abstract

We have mapped 17 extragenic suppressors of benA33, a heat-sensitive beta-tubulin mutation of Aspergillus nidulans, to the tubA alpha tubulin locus. Fifteen of these tubA mutations cause cold sensitivity in a genetic background with benA33 and appear to cause lethality in a background with the wild-type benA allele. We examined the microtubule-mediated processes, nuclear division and nuclear migration, in seven different cold-sensitive double mutants, each carrying benA33 and a different cold-sensitive tubA allele. Nuclear division and migration were inhibited at a restrictive temperature in each case, suggesting that cold sensitivity is due to the inhibition of microtubule function at low temperatures. A single allele, tubA4, suppressed the heat sensitivity conferred by benA33 but did not confer cold sensitivity in a benA33 background, however in a wild-type benA background, tubA4 conferred supersensitivity to antimicrotubule agents and weak cold sensitivity. TubA4 did not suppress the heat sensitivity conferred by two other benA alleles. The cold sensitivity conferred by tubA4 was suppressed by the microtubule stabilizing agent deuterium oxide, and the suppression of heat sensitivity conferred by four other tubA mutations was reversed by deuterium oxide. These results suggest that these mutations may affect hydrophobic interactions between alpha- and beta-tubulin.

摘要

我们已将烟曲霉热敏感β-微管蛋白突变benA33的17个基因外抑制子定位到tubAα-微管蛋白基因座。其中15个tubA突变在benA33的遗传背景下导致冷敏感,在野生型benA等位基因的背景下似乎导致致死性。我们研究了七个不同的冷敏感双突变体中的微管介导过程、核分裂和核迁移,每个双突变体都携带benA33和一个不同的冷敏感tubA等位基因。在每种情况下,核分裂和迁移在限制温度下均受到抑制,这表明冷敏感是由于低温下微管功能受到抑制。单个等位基因tubA4抑制了benA33赋予的热敏感性,但在benA33背景下不赋予冷敏感性,然而在野生型benA背景下,tubA4赋予对抗微管药物的超敏感性和弱冷敏感性。tubA4不抑制其他两个benA等位基因赋予的热敏感性。tubA4赋予的冷敏感性被微管稳定剂氧化氘抑制,其他四个tubA突变赋予的热敏感性抑制被氧化氘逆转。这些结果表明,这些突变可能影响α-微管蛋白和β-微管蛋白之间的疏水相互作用。

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