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Alanine-scanning mutagenesis of Aspergillus gamma-tubulin yields diverse and novel phenotypes.对曲霉γ-微管蛋白进行丙氨酸扫描诱变可产生多样且新颖的表型。
Mol Biol Cell. 2001 Jul;12(7):2119-36. doi: 10.1091/mbc.12.7.2119.
2
Mitosis in wild-type and beta-tubulin mutant strains of Aspergillus nidulans.构巢曲霉野生型和β-微管蛋白突变体菌株中的有丝分裂。
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3
Gamma-tubulin and the C-terminal motor domain kinesin-like protein, KLPA, function in the establishment of spindle bipolarity in Aspergillus nidulans.γ-微管蛋白和C端运动结构域驱动蛋白样蛋白KLPA在构巢曲霉纺锤体双极性的建立中发挥作用。
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4
Tubulins in Aspergillus nidulans.构巢曲霉中的微管蛋白。
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8
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1
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9
The functions of myosin II and myosin V homologs in tip growth and septation in Aspergillus nidulans.肌球蛋白 II 和肌球蛋白 V 同源物在 Aspergillus nidulans 顶端生长和分隔中的功能。
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10
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本文引用的文献

1
Gamma-tubulin: the microtubule organizer?γ-微管蛋白:微管组织中心?
Trends Cell Biol. 1992 Jan;2(1):1-5. doi: 10.1016/0962-8924(92)90125-7.
2
The genetics of Aspergillus nidulans.构巢曲霉的遗传学
Adv Genet. 1953;5:141-238. doi: 10.1016/s0065-2660(08)60408-3.
3
Structural models for the self-assembly and microtubule interactions of gamma-, delta- and epsilon-tubulin.γ-、δ-和ε-微管蛋白的自组装及与微管相互作用的结构模型
J Cell Sci. 2001 Jan;114(Pt 2):413-22. doi: 10.1242/jcs.114.2.413.
4
The carboxy terminus of Tub4p is required for gamma-tubulin function in budding yeast.Tub4p的羧基末端对于芽殖酵母中的γ-微管蛋白功能是必需的。
J Cell Sci. 2000 Nov;113 Pt 21:3871-82. doi: 10.1242/jcs.113.21.3871.
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gamma-Tubulin.γ-微管蛋白
Curr Top Dev Biol. 2000;49:27-54. doi: 10.1016/s0070-2153(99)49003-9.
6
Gamma-tubulin nucleation: template or protofilament?γ-微管蛋白成核:模板还是原丝?
Nat Cell Biol. 2000 Jun;2(6):E93-6. doi: 10.1038/35014084.
7
Structure of the gamma-tubulin ring complex: a template for microtubule nucleation.γ-微管蛋白环复合物的结构:微管成核的模板。
Nat Cell Biol. 2000 Jun;2(6):365-70. doi: 10.1038/35014058.
8
A new function for the gamma-tubulin ring complex as a microtubule minus-end cap.γ-微管蛋白环复合物作为微管负端帽的新功能。
Nat Cell Biol. 2000 Jun;2(6):358-64. doi: 10.1038/35014051.
9
Immunostructural evidence for the template mechanism of microtubule nucleation.微管成核模板机制的免疫结构证据。
Nat Cell Biol. 2000 Jun;2(6):352-7. doi: 10.1038/35014045.
10
Suppression of microtubule dynamic instability and treadmilling by deuterium oxide.重水对微管动态不稳定性及踏车行为的抑制作用
Biochemistry. 2000 May 2;39(17):5075-81. doi: 10.1021/bi992217f.

对曲霉γ-微管蛋白进行丙氨酸扫描诱变可产生多样且新颖的表型。

Alanine-scanning mutagenesis of Aspergillus gamma-tubulin yields diverse and novel phenotypes.

作者信息

Jung M K, Prigozhina N, Oakley C E, Nogales E, Oakley B R

机构信息

Department of Molecular Genetics, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

Mol Biol Cell. 2001 Jul;12(7):2119-36. doi: 10.1091/mbc.12.7.2119.

DOI:10.1091/mbc.12.7.2119
PMID:11452008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC55667/
Abstract

We have created 41 clustered charged-to-alanine scanning mutations of the mipA, gamma-tubulin, gene of Aspergillus nidulans and have created strains carrying these mutations by two-step gene replacement and by a new procedure, heterokaryon gene replacement. Most mutant alleles confer a wild-type phenotype, but others are lethal or conditionally lethal. The conditionally lethal alleles exhibit a variety of phenotypes under restrictive conditions. Most have robust but highly abnormal mitotic spindles and some have abnormal cytoplasmic microtubule arrays. Two alleles appear to have reduced amounts of gamma-tubulin at the spindle pole bodies and nucleation of spindle microtubule assembly may be partially inhibited. One allele inhibits germ tube formation. The cold sensitivity of two alleles is strongly suppressed by the antimicrotubule agents benomyl and nocodazole and a third allele is essentially dependent on these compounds for growth. Together our data indicate that gamma-tubulin probably carries out functions essential to mitosis and organization of cytoplasmic microtubules in addition to its well-documented role in microtubule nucleation. We have also placed our mutations on a model of the structure of gamma-tubulin and these data give a good initial indication of the functionally important regions of the molecule.

摘要

我们构建了构巢曲霉mipA(γ-微管蛋白)基因的41个成簇的电荷到丙氨酸扫描突变体,并通过两步基因置换和一种新方法——异核体基因置换,构建了携带这些突变的菌株。大多数突变等位基因表现出野生型表型,但其他一些则是致死的或条件致死的。条件致死等位基因在限制条件下表现出多种表型。大多数具有粗壮但高度异常的有丝分裂纺锤体,有些具有异常的细胞质微管阵列。两个等位基因似乎在纺锤极体处的γ-微管蛋白含量减少,纺锤体微管组装的成核可能受到部分抑制。一个等位基因抑制芽管形成。抗微管药物苯菌灵和诺考达唑强烈抑制两个等位基因的冷敏感性,第三个等位基因的生长基本上依赖于这些化合物。我们的数据共同表明,γ-微管蛋白除了在微管成核中已被充分证明的作用外,可能还执行着对有丝分裂和细胞质微管组织至关重要的功能。我们还将我们的突变定位到γ-微管蛋白的结构模型上,这些数据初步很好地表明了该分子的功能重要区域。