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Structure of sterol aliphatic chains affects yeast cell shape and cell fusion during mating

机译:固醇脂族链的结构影响交配过程中酵母细胞的形状和细胞融合

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摘要

Under mating conditions, yeast cells adopt a characteristic pear-shaped morphology, called a "shmoo," as they project a cell extension toward their mating partners. Mating partners make contact at their shmoo tips, dissolve the intervening cell wall, and fuse their plasma membranes. We identified mutations in ERG4, encoding the enzyme that catalyzes the last step of ergosterol biosynthesis, that impair both shmoo formation and cell fusion. Upon pheromone treatment, erg4△ mutants polarized growth, lipids, and proteins involved in mating but did not form properly shaped shmoos and fused with low efficiency. Supplementation with ergosterol partially suppressed the shmooing defect but not the cell fusion defect. By contrast, removal of the Erg4 substrate ergosta-5,7,22,24(28)-tetraenol, which accumulates in erg△ mutant cells and contains an extra double bond in the aliphatic chain of the sterol, restored both shmooing and cell fusion to wild-type levels. Thus, a two-atom change in the aliphatic moiety of ergosterol is sufficient to obstruct cell shape remodeling and cell fusion.
机译:在交配条件下,酵母细胞会向其交配伴侣投射细胞延伸,因此具有一种称为“ shmoo”的特征性梨形形态。交配伴侣在其shmoo尖端接触,溶解介入的细胞壁,并融合其质膜。我们鉴定了ERG4的突变,该突变编码的酶催化麦角固醇生物合成的最后一步,损害了shmoo的形成和细胞融合。信息素处理后,erg4△突变体使交配中的生长,脂质和蛋白质极化,但未形成适当形状的shmoos并以低效率融合。麦角固醇的补充部分抑制了shmooing缺陷,但没有抑制细胞融合缺陷。相比之下,去除Erg4底物ergosta-5、7、22、24(28)-丁烯醇(其积聚在erg△突变细胞中,并且在甾醇的脂族链中包含一个额外的双键),恢复了shmooing和细胞融合达到野生型水平。因此,麦角固醇的脂族部分中的两个原子变化足以阻碍细胞形状重塑和细胞融合。

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    Howard Hughes Medical Institute, University of California, San Francisco, CA 94158 Departments of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;

    rnHoward Hughes Medical Institute, University of California, San Francisco, CA 94158 Departments of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;

    rnHoward Hughes Medical Institute, University of California, San Francisco, CA 94158 Departments of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;

    rnHoward Hughes Medical Institute, University of California, San Francisco, CA 94158 Departments of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;

    rnMax Planck Institute for Molecular Cell Biology and Genetics, D-01307 Dresden, Germany;

    rnDepartments of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94158;

    rnMax Planck Institute for Molecular Cell Biology and Genetics, D-01307 Dresden, Germany;

    rnHoward Hughes Medical Institute, University of California, San Francisco, CA 94158 Departments of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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