首页> 美国卫生研究院文献>Genetics >The external amino acid signaling pathway promotes activation of Stp1 and Uga35/Dal81 transcription factors for induction of the AGP1 gene in Saccharomyces cerevisiae.
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The external amino acid signaling pathway promotes activation of Stp1 and Uga35/Dal81 transcription factors for induction of the AGP1 gene in Saccharomyces cerevisiae.

机译:外部氨基酸信号转导途径可促进Stp1和Uga35 / Dal81转录因子的激活从而诱导酿酒酵母中的AGP1基因。

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摘要

Yeast cells respond to the presence of amino acids in their environment by inducing transcription of several amino acid permease genes including AGP1, BAP2, and BAP3. The signaling pathway responsible for this induction involves Ssy1, a permease-like sensor of external amino acids, and culminates with proteolytic cleavage and translocation to the nucleus of the zinc-finger proteins Stp1 and Stp2, the lack of which abolishes induction of BAP2 and BAP3. Here we show that Stp1-but not Stp2-plays an important role in AGP1 induction, although significant induction of AGP1 by amino acids persists in stp1 and stp1 stp2 mutants. This residual induction depends on the Uga35/Dal81 transcription factor, indicating that the external amino acid signaling pathway activates not only Stp1 and Stp2, but also another Uga35/Dal81-dependent transcriptional circuit. Analysis of the AGP1 gene's upstream region revealed that Stp1 and Uga35/Dal81 act synergistically through a 21-bp cis-acting sequence similar to the UAS(AA) element previously found in the BAP2 and BAP3 upstream regions. Although cells growing under poor nitrogen-supply conditions display much higher induction of AGP1 expression than cells growing under good nitrogen-supply conditions, the UAS(AA) itself is totally insensitive to nitrogen availability. Nitrogen-source control of AGP1 induction is mediated by the GATA factor Gln3, likely acting through adjacent 5'-GATA-3' sequences, to amplify the positive effect of UAS(AA). Our data indicate that Stp1 may act in combination with distinct sets of transcription factors, according to the gene context, to promote induction of transcription in response to external amino acids. The data also suggest that Uga35/Dal81 is yet another transcription factor under the control of the external amino acid sensing pathway. Finally, the data show that the TOR pathway mediating global nitrogen control of transcription does not interfere with the external amino acid signaling pathway.
机译:酵母细胞通过诱导几种氨基酸渗透酶基因(包括AGP1,BAP2和BAP3)的转录来响应其环境中氨基酸的存在。引起这种诱导的信号传导途径涉及Ssy1,一种外部氨基酸的类似渗透酶的传感器,并最终通过蛋白水解酶裂解并易位到锌指蛋白Stp1和Stp2的核中,缺乏该蛋白消除了BAP2和BAP3的诱导。 。在这里我们显示Stp1但不是Stp2在AGP1诱导中起重要作用,尽管在stp1和stp1 stp2突变体中氨基酸对AGP1的显着诱导仍然存在。这种残留的诱导取决于Uga35 / Dal81转录因子,表明外部氨基酸信号传导途径不仅激活Stp1和Stp2,而且激活了另一个Uga35 / Dal81依赖的转录回路。 AGP1基因上游区域的分析表明,Stp1和Uga35 / Dal81通过21 bp的顺式作用序列协同作用,该序列类似于先前在BAP2和BAP3上游区域中发现的UAS(AA)元件。尽管在氮供应不良的条件下生长的细胞比在氮供应良好的条件下生长的细胞显示出更高的AGP1表达诱导能力,但UAS(AA)本身对氮的可用性完全不敏感。 AGP1诱导的氮源控制是由GATA因子Gln3介导的,可能通过相邻的5'-GATA-3'序列起作用,以放大UAS(AA)的积极作用。我们的数据表明Stp1可能与转录因子的不同集合结合,根据基因环境,促进响应外部氨基酸的转录诱导。数据还表明,Uga35 / Dal81是在外部氨基酸传感途径控制下的又一个转录因子。最后,数据表明介导转录的总体氮控制的TOR途径不干扰外部氨基酸信号传导途径。

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