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Asymmetrically localized Bud8p and Bud9p proteins control yeast cell polarity and development

机译:不对称定位的Bud8p和Bud9p蛋白控制酵母细胞的极性和发育

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摘要

Diploid strains of the budding yeast Saccharomyces cerevisiae change the pattern of cell division from bipolar to unipolar when switching growth from the unicellular yeast form (YF) to filamentous, pseudohyphal (PH) cells in response to nitrogen starvation. The functions of two transmembrane proteins, Bud8p and Bud9p, in regulating YF and PH cell polarity were investigated. Bud8p is highly concentrated at the distal pole of both YF and PH cells, where it directs initiation of cell division. Asymmetric localization of Bud8p is independent of the Rsr1p/Bud1p GTPase. rsr1/bud1 mutations are epistatic to bud8 mutations, placing Rsr1p/Bud1p downstream of Bud8p. In YF cells, Bud9p is also localized at the distal pole, yet deletion of BUD9 favours distal bud initiation. In PH cells, nutritional starvation for nitrogen efficiently prevents distal localization of Bud9p. Because Bud8p and Bud9p proteins associate in vivo, we propose Bud8p as a landmark for bud initiation at the distal cell pole, where Bud9p acts as inhibitor. In response to nitrogen starvation, asymmetric localization of Bud9p is averted, favouring Bud8p-mediated cell division at the distal pole.
机译:当将生长从单细胞酵母形式(YF)转变为丝状假菌丝(PH)细胞以响应氮饥饿时,发芽酵母酿酒酵母的二倍体菌株将细胞分裂的模式从双极转变为单极。研究了两种跨膜蛋白Bud8p和Bud9p在调节YF和PH细胞极性方面的功能。 Bud8p高度集中在YF和PH细胞的远端,指导细胞分裂的开始。 Bud8p的不对称定位独立于Rsr1p / Bud1p GTPase。 rsr1 / bud1突变是bud8突变的上位基因,将Rsr1p / Bud1p置于Bud8p的下游。在YF细胞中,Bud9p也位于远端,但是BUD9的缺失有利于远端芽的萌发。在PH细胞中,氮的营养饥饿有效地阻止了Bud9p的远端定位。由于Bud8p和Bud9p蛋白在体内缔合,因此我们建议Bud8p作为远端细胞极处芽萌生的标志,而Bud9p充当抑制剂。响应氮饥饿,避免了Bud9p的不对称定位,有利于Bud8p介导的远端细胞分裂。

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