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首页> 外文期刊>Molecular and Cellular Biology >The Cbk1p Pathway Is Important for Polarized Cell Growth and Cell Separation in Saccharomyces cerevisiae
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The Cbk1p Pathway Is Important for Polarized Cell Growth and Cell Separation in Saccharomyces cerevisiae

机译:Cbk1p通路对酿酒酵母中的极化细胞生长和细胞分离很重要。

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摘要

During the early stages of budding, cell wall remodeling and polarized secretion are concentrated at the bud tip (apical growth). The CBK1 gene, encoding a putative serine/threonine protein kinase, was identified in a screen designed to isolate mutations that affect apical growth. Analysis of cbk1Δ cells reveals that Cbk1p is required for efficient apical growth, proper mating projection morphology, bipolar bud site selection in diploid cells, and cell separation. Epitope-tagged Cbk1p localizes to both sides of the bud neck in late anaphase, just prior to cell separation.CBK1 and another gene, HYM1, were previously identified in a screen for genes involved in transcriptional repression and proposed to function in the same pathway. Deletion ofHYM1 causes phenotypes similar to those observed incbk1Δ cells and disrupts the bud neck localization of Cbk1p. Whole-genome transcriptional analysis of cbk1Δsuggests that the kinase regulates the expression of a number of genes with cell wall-related functions, including two genes required for efficient cell separation: the chitinase-encoding gene CTS1and the glucanase-encoding gene SCW11. The Ace2p transcription factor is required for expression of CTS1 and has been shown to physically interact with Cbk1p. Analysis oface2Δ cells reveals that Ace2p is required for cell separation but not for polarized growth. Our results suggest that Cbk1p and Hym1p function to regulate two distinct cell morphogenesis pathways: an ACE2-independent pathway that is required for efficient apical growth and mating projection formation and anACE2-dependent pathway that is required for efficient cell separation following cytokinesis. Cbk1p is most closely related to theNeurospora crassa Cot-1; Schizosaccharomyces pombe Orb6; Caenorhabditis elegans, Drosophila, and human Ndr; and Drosophila and mammalian WARTS/LATS kinases. Many Cbk1-related kinases have been shown to regulate cellular morphology.
机译:在出芽的早期阶段,细胞壁重塑和极化分泌物集中在芽尖(顶端生长)。在旨在隔离影响顶端生长的突变的筛选中鉴定了编码假定的丝氨酸/苏氨酸蛋白激酶的 CBK1 基因。对cbk1Δ细胞的分析表明,Cbk1p是有效的根尖生长,正确的交配投射形态,二倍体细胞中双极芽位点选择和细胞分离所必需的。带有表位标记的Cbk1p在后期后期,即在细胞分离之前,位于芽颈的两侧。 CBK1 和另一个基因 HYM1 在筛选前已被鉴定出来。基因参与转录抑制,并建议在同一途径中发挥作用。删除 HYM1 导致表型类似于在cbk1Δ细胞中观察到的表型,并破坏Cbk1p的芽颈定位。 cbk1Δ的全基因组转录分析表明,该激酶调节许多具有细胞壁相关功能的基因的表达,包括有效分离细胞所需的两个基因:几丁质酶编码基因 CTS1 和葡聚糖酶编码基因 SCW11 。 Ace2p转录因子是表达 CTS1 所必需的,并且已显示与Cbk1p发生物理相互作用。对ace2Δ细胞的分析表明,Ace2p是细胞分离所必需的,而不是极化生长所必需的。我们的结果表明,Cbk1p和Hym1p的功能是调节两个不同的细胞形态发生途径: ACE2 独立途径,这是有效的根尖生长和交配投射形成所必需的;而 ACE2 -胞质分裂后有效细胞分离所需的依赖途径。 Cbk1p与 Neurospora crassa Cot-1关系最密切。 粟酒裂殖酵母 Orb6; 秀丽隐杆线虫,果蝇和人类Ndr;和果蝇和哺乳动物WARTS / LATS激酶。已显示许多与Cbk1相关的激酶可调节细胞形态。

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