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酿酒酵母氮饥饿诱导的Yvh1p和Ptp2p磷酸酶在孢子形成的控制中发挥作用。

The S. cerevisiae nitrogen starvation-induced Yvh1p and Ptp2p phosphatases play a role in control of sporulation.

作者信息

Park H D, Beeser A E, Clancy M J, Cooper T G

机构信息

Department of Microbiology and Immunology, University of Tennessee, Memphis 38163, USA.

出版信息

Yeast. 1996 Sep 15;12(11):1135-51. doi: 10.1002/(sici)1097-0061(19960915)12:11<1135::aid-yea11>3.0.co;2-l.

Abstract

Starvation for nitrogen in the absence of a fermentable carbon source causes diploid Saccharomyces cerevisiae cells to leave vegetative growth, enter meiosis, and sporulare; the former nutritional condition also induces expression of the YVH1 gene that encodes a protein phosphatase. This correlation prompted us to determine whether the Yvh1p phosphatase was a participant in the network that controls the onset of meiosis and sporulation. We found that expression of the IME2 gene, encoding a protein kinase homologue required for meiosis- and sporulation-specific gene expression, is decreased in a yvh1 disrupted strain. We also observed a decrease, albeit a smaller one, in the expression of IME1 which encodes an activator protein required for IME2 expression. Under identical experimental conditions, expression of the MCKI and IME4 genes (which promote sporulation but do not require Ime1p for expression) was not affected. These results demonstrate the specificity of the yvh1 disruption phenotype. They suggest that decreased steady-state levels of IME1 and IME2 mRNA were not merely the result of non-specific adverse affects on nucleic acid metabolism caused by the yvh1 disruption. Sporulation of a homozygous yvh1 disruption mutant was delayed and less efficient overall compared to an isogenic wild-type strain, a result which correlates with decreased IME1 and IME2 gene expression. We also observed that expression of the PTP2 tyrosine phosphatase gene (a negative regulator of the osmosensing MAP kinase cascade), but not the PTP1 gene (also encoding a tyrosine phosphatase) was induced by nitrogen-starvation. Although disruption of PTP2 alone did not demonstrably affect sporulation or IME2 gene expression, sporulation was decreased more in a yvh1, ptp2 double mutant than in a yvh1 single mutant; it was nearly abolished in the double mutant. These data suggest that the YVH1 and PTP2 encoded phosphatases likely participate in the control network regulating meiosis and sporulation. Expression of YVH1 and PTP2 was not affected by nitrogen source quality (asparagine compared to proline) suggesting that nitrogen starvation-induced YVH1 and PTP2 expression and sensitivity to nitrogen catabolite repression are on two different branches of the nitrogen regulatory network.

摘要

在缺乏可发酵碳源的情况下,氮饥饿会导致二倍体酿酒酵母细胞停止营养生长,进入减数分裂并形成孢子;前一种营养条件还会诱导编码蛋白磷酸酶的YVH1基因的表达。这种相关性促使我们确定Yvh1p磷酸酶是否参与了控制减数分裂和孢子形成起始的网络。我们发现,在yvh1缺失菌株中,编码减数分裂和孢子形成特异性基因表达所需的蛋白激酶同源物的IME2基因的表达降低。我们还观察到,编码IME2表达所需的激活蛋白的IME1的表达也有所下降,尽管下降幅度较小。在相同的实验条件下,促进孢子形成但表达不需要Ime1p的MCKI和IME4基因的表达不受影响。这些结果证明了yvh1缺失表型的特异性。它们表明,IME1和IME2 mRNA稳态水平的降低不仅仅是yvh1缺失对核酸代谢造成的非特异性不利影响的结果。与同基因野生型菌株相比,纯合yvh1缺失突变体的孢子形成延迟,总体效率较低,这一结果与IME1和IME2基因表达的降低相关。我们还观察到,氮饥饿会诱导PTP2酪氨酸磷酸酶基因(渗透感应MAP激酶级联的负调节因子)的表达,但不会诱导PTP1基因(也编码酪氨酸磷酸酶)的表达。虽然单独破坏PTP2并没有明显影响孢子形成或IME2基因表达,但yvh1、ptp2双突变体中的孢子形成比yvh1单突变体中的孢子形成减少得更多;在双突变体中几乎完全消除。这些数据表明,YVH1和PTP2编码的磷酸酶可能参与了调节减数分裂和孢子形成的控制网络。YVH1和PTP2的表达不受氮源质量(天冬酰胺与脯氨酸相比)的影响,这表明氮饥饿诱导的YVH1和PTP2表达以及对氮分解代谢物阻遏的敏感性位于氮调节网络的两个不同分支上。

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