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Role of Bud3p in producing the axial budding pattern of yeast

机译:Bud3p在产生酵母的轴向出芽模式中的作用

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摘要

Yeast cells can select bud sites in either of two distinct spatial patterns. a cells and alpha cells typically bud in an axial pattern, in which both mother and daughter cells form new buds adjacent to the preceding division site. In contrast, a/alpha cells typically bud in a bipolar pattern, in which new buds can form at either pole of the cell. The BUD3 gene is specifically required for the axial pattern of budding: mutations of BUD3 (including a deletion) affect the axial pattern but not the bipolar pattern. The sequence of BUD3 predicts a product (Bud3p) of 1635 amino acids with no strong or instructive similarities to previously known proteins. However, immunofluorescence localization of Bud3p has revealed that it assembles in an apparent double ring encircling the mother-bud neck shortly after the mitotic spindle forms. The Bud3p structure at the neck persists until cytokinesis, when it splits to yield a single ring of Bud3p marking the division site on each of the two progeny cells. These single rings remain for much of the ensuing unbudded phase and then disassemble. The Bud3p rings are indistinguishable from those of the neck filament- associated proteins (Cdc3p, Cdc10p, Cdc11p, and Cdc12p), except that the latter proteins assemble before bud emergence and remain in place for the duration of the cell cycle. Upon shift of a temperature- sensitive cdc12 mutant to restrictive temperature, localization of both Bud3p and the neck filament-associated proteins is rapidly lost. In addition, a haploid cdc11 mutant loses its axial-budding pattern upon shift to restrictive temperature. Taken together, the data suggest that Bud3p and the neck filaments are linked in a cycle in which each controls the position of the other's assembly: Bud3p assembles onto the neck filaments in one cell cycle to mark the site for axial budding (including assembly of the new ring of neck filaments) in the next cell cycle. As the expression and localization of Bud3p are similar in a, alpha, and a/alpha cells, additional regulation must exist such that Bud3p restricts the position of bud formation in a and alpha cells but not in a/alpha cells.
机译:酵母细胞可以两种不同的空间模式中的任意一种来选择芽位点。细胞和α细胞通常以轴向模式萌芽,其中母细胞和子细胞都形成与先前分裂位点相邻的新芽。相反,a / alpha细胞通常以双极性模式出芽,其中新的芽可以在细胞的任一极形成。 BUD3基因是出芽的轴向模式特别需要的:BUD3的突变(包括缺失)影响轴向模式,但不影响双极模式。 BUD3的序列可预测具有1635个氨基酸的产物(Bud3p),与先前已知的蛋白质没有强烈或具有指导意义的相似性。但是,Bud3p的免疫荧光定位表明,在有丝分裂纺锤体形成后不久,它会在一个明显的双环中组装,环绕母芽颈部。脖子上的Bud3p结构一直持续到胞质分裂为止,当它分裂产生单个Bud3p环时,标志着两个子代细胞各自的分裂位点。这些单环在接下来的大部分未预算阶段中都会保留下来,然后分解。 Bud3p环与与颈部细丝相关的蛋白(Cdc3p,Cdc10p,Cdc11p和Cdc12p)的环没有区别,只是后者的蛋白在芽出芽前组装并在细胞周期的整个过程中保持原位。将温度敏感的cdc12突变体转变为限制性温度后,Bud3p和与颈部细丝相关的蛋白质的定位都迅速消失。此外,单倍体cdc11突变体在转移至限制性温度后会失去其轴向萌芽模式。综上所述,数据表明,Bud3p和颈部细丝以一个周期相连,每个周期都控制对方的装配位置:Bud3p在一个细胞周期内装配到颈部细丝上,以标记轴向出芽的位置(包括在下一个细胞周期中产生新的颈环。由于Bud3p在a,alpha和a / alpha细胞中的表达和定位相似,因此必须存在额外的调节,以使Bud3p限制a和alpha细胞中芽形成的位置,而不限制a / alpha细胞中的芽形成位置。

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