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酵母肽类信息素,即a-因子和α-因子,在其靶细胞中激活共同的反应机制。

Yeast peptide pheromones, a-factor and alpha-factor, activate a common response mechanism in their target cells.

作者信息

Bender A, Sprague G F

出版信息

Cell. 1986 Dec 26;47(6):929-37. doi: 10.1016/0092-8674(86)90808-1.

DOI:10.1016/0092-8674(86)90808-1
PMID:3022943
Abstract

We show that in yeast the cell type specificity of pheromone response is determined solely by the species of receptor that a cell synthesizes. The two receptor-pheromone interactions are functionally interchangeable and involve the creation of a common intracellular signal. In particular, we find that provision of a-factor receptor or alpha-factor receptor in mat alpha 1 mutants, which normally do not express either receptor or any other a- or alpha-specific products, allows response to the appropriate pheromone. Moreover, provision of a-factor receptor in a cells lacking alpha-factor receptor restores mating competence to those cells. Finally, an aspect of pheromone response that is normally unique to a-factor action on alpha cells--increased transcription from the alpha-specific STE3 gene--can also be observed following alpha-factor treatment of pseudo-a cells (mat alpha 2 ste3 ste13), special mutants that respond to alpha-factor and also have an active STE3 promoter.

摘要

我们发现,在酵母中,信息素反应的细胞类型特异性完全由细胞合成的受体种类决定。两种受体 - 信息素相互作用在功能上是可互换的,并且涉及共同细胞内信号的产生。具体而言,我们发现,在通常不表达任何一种受体或任何其他a - 或α - 特异性产物的matα1突变体中提供a - 因子受体或α - 因子受体,可使细胞对相应的信息素产生反应。此外,在缺乏α - 因子受体的a细胞中提供a - 因子受体可恢复这些细胞的交配能力。最后,在对α - 因子有反应且具有活性STE3启动子的特殊突变体——假a细胞(matα2 ste3 ste13)经α - 因子处理后,也能观察到信息素反应中通常是a - 因子作用于α细胞所特有的一个方面——α - 特异性STE3基因转录增加。

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Yeast peptide pheromones, a-factor and alpha-factor, activate a common response mechanism in their target cells.酵母肽类信息素,即a-因子和α-因子,在其靶细胞中激活共同的反应机制。
Cell. 1986 Dec 26;47(6):929-37. doi: 10.1016/0092-8674(86)90808-1.
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Evidence the yeast STE3 gene encodes a receptor for the peptide pheromone a factor: gene sequence and implications for the structure of the presumed receptor.酵母STE3基因编码肽类信息素α因子受体的证据:基因序列及其对假定受体结构的影响。
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J Mol Biol. 1984 Oct 5;178(4):835-52. doi: 10.1016/0022-2836(84)90314-0.

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