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酵母中由突变和过表达引起的双极出芽的破坏。

Mutational and hyperexpression-induced disruption of bipolar budding in yeast.

作者信息

Freedman Toby, Porter Alexandra, Haarer Brian

机构信息

Section of Molecular Cell and Developmental Biology, The University of Texas, Austin, TX 78712, USA2.

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, MA 02138, USA1.

出版信息

Microbiology (Reading). 2000 Nov;146 ( Pt 11):2833-2843. doi: 10.1099/00221287-146-11-2833.

DOI:10.1099/00221287-146-11-2833
PMID:11065362
Abstract

Analysis of bud-site selection in the yeast Saccharomyces cerevisiae has helped to identify many genes that are generally important for eukaryotic cell polarization. Colony morphology screens were used to identify factors relevant to the process of bipolar budding in yeast. Mutants defective in bipolar budding were identified by virtue of their inability to grow as pseudohyphae in a haploid bud3 background. A mutant allele of the MYO2 gene, encoding a class-V unconventional myosin was identified that perturbs bipolar budding without affecting axial budding and without grossly affecting the role of Myo2p in secretion and maintenance of the actin cytoskeleton. Several genes were also identified whose products, when overexpressed, are capable of disrupting bipolar budding. Among these are the actin-monomer-binding protein profilin and the Aip3p/Bud6p-interacting protein Atc1p. The results strongly support involvement of the actin cytoskeleton in the establishment of bipolar budding and in the maintenance of pseudohyphal growth.

摘要

对酿酒酵母芽位选择的分析有助于鉴定许多对真核细胞极化普遍重要的基因。通过菌落形态筛选来鉴定与酵母双极出芽过程相关的因子。在单倍体bud3背景下,不能以假菌丝形式生长的突变体被鉴定为双极出芽缺陷型。鉴定出一个编码V类非常规肌球蛋白的MYO2基因突变等位基因,它扰乱双极出芽,但不影响轴向出芽,也不严重影响Myo2p在肌动蛋白细胞骨架分泌和维持中的作用。还鉴定出几个基因,其产物在过表达时能够破坏双极出芽。其中包括肌动蛋白单体结合蛋白原肌球蛋白以及与Aip3p/Bud6p相互作用的蛋白Atc1p。结果有力地支持了肌动蛋白细胞骨架参与双极出芽的建立和假菌丝生长的维持。

相似文献

1
Mutational and hyperexpression-induced disruption of bipolar budding in yeast.酵母中由突变和过表达引起的双极出芽的破坏。
Microbiology (Reading). 2000 Nov;146 ( Pt 11):2833-2843. doi: 10.1099/00221287-146-11-2833.
2
Immunofluorescence localization of the unconventional myosin, Myo2p, and the putative kinesin-related protein, Smy1p, to the same regions of polarized growth in Saccharomyces cerevisiae.酿酒酵母中非常规肌球蛋白Myo2p和假定的驱动蛋白相关蛋白Smy1p在极化生长相同区域的免疫荧光定位。
J Cell Biol. 1994 May;125(4):825-42. doi: 10.1083/jcb.125.4.825.
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The secretory pathway mediates localization of the cell polarity regulator Aip3p/Bud6p.分泌途径介导细胞极性调节因子Aip3p/Bud6p的定位。
Mol Biol Cell. 2000 Feb;11(2):647-61. doi: 10.1091/mbc.11.2.647.
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Type II myosin heavy chain encoded by the myo2 gene composes the contractile ring during cytokinesis in Schizosaccharomyces pombe.由myo2基因编码的II型肌球蛋白重链在粟酒裂殖酵母的胞质分裂过程中组成收缩环。
J Cell Biol. 1997 Jun 16;137(6):1309-19. doi: 10.1083/jcb.137.6.1309.
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Type II myosin involved in cytokinesis in the fission yeast, Schizosaccharomyces pombe.II型肌球蛋白参与裂殖酵母粟酒裂殖酵母的胞质分裂过程。
Cell Motil Cytoskeleton. 1997;38(4):385-96. doi: 10.1002/(SICI)1097-0169(1997)38:4<385::AID-CM8>3.0.CO;2-2.
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Sro7p, a Saccharomyces cerevisiae counterpart of the tumor suppressor l(2)gl protein, is related to myosins in function.Sro7p是肿瘤抑制蛋白l(2)gl的酿酒酵母对应物,在功能上与肌球蛋白相关。
Genetics. 1998 Aug;149(4):1717-27. doi: 10.1093/genetics/149.4.1717.
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The tail of a yeast class V myosin, myo2p, functions as a localization domain.酵母V类肌球蛋白myo2p的尾部作为一个定位结构域发挥作用。
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The yeast kinesin-related protein Smy1p exerts its effects on the class V myosin Myo2p via a physical interaction.酵母驱动蛋白相关蛋白Smy1p通过物理相互作用对V类肌球蛋白Myo2p发挥作用。
Mol Biol Cell. 2000 Feb;11(2):691-702. doi: 10.1091/mbc.11.2.691.
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Two distinct regions in a yeast myosin-V tail domain are required for the movement of different cargoes.酵母肌球蛋白-V尾部结构域中的两个不同区域是不同货物运输所必需的。
J Cell Biol. 2000 Aug 7;150(3):513-26. doi: 10.1083/jcb.150.3.513.
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Fission yeast Rng3p: an UCS-domain protein that mediates myosin II assembly during cytokinesis.裂殖酵母Rng3p:一种在胞质分裂过程中介导肌球蛋白II组装的UCS结构域蛋白。
J Cell Sci. 2000 Jul;113 ( Pt 13):2421-32. doi: 10.1242/jcs.113.13.2421.

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