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Conserved and Diverged Functions of the Calcineurin-Activated Prz1 Transcription Factor in Fission Yeast

机译:钙调磷酸酶激活的Prz1转录因子在裂变酵母中的保守和分散功能。

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摘要

Gene regulation in response to intracellular calcium is mediated by the calcineurin-activated transcription factor Prz1 in the fission yeast Schizosaccharomyces pombe. Genome-wide studies of the and CrzA fungal orthologs have uncovered numerous target genes involved in conserved and species-specific cellular processes. In contrast, very few target genes of Prz1 have been published. This article identifies an extensive list of genes using transcriptome and ChIP-chip analyses under inducing conditions of Prz1, including CaCl2 and tunicamycin treatment, as well as a ∆pmr1 genetic background. We identified 165 upregulated putative target genes of Prz1 in which the majority contained a calcium-dependent response element in their promoters, similar to that of the Saccharomyces cerevisiae ortholog . These genes were functionally enriched for -conserved processes such as cell-wall biosynthesis. Overexpression of prz1+ increased resistance to the cell-wall degradation enzyme zymolyase, likely from upregulation of the O-mannosyltransferase encoding gene omh1+. Loss of omh1+ abrogates this phenotype. We uncovered a novel inhibitory role in flocculation for Prz1. Loss of prz1+ resulted in constitutive flocculation and upregulation of genes encoding the flocculins Gsf2 and Pfl3, as well as the transcription factor Cbf12. The constitutive flocculation of the ∆prz1 strain was abrogated by the loss of gsf2+ or cbf12+. This study reveals that Prz1 functions as a positive and negative transcriptional regulator of genes involved in cell-wall biosynthesis and flocculation, respectively. Moreover, comparison of target genes between /CrzA and Prz1 indicate some conservation in DNA-binding specificity, but also substantial rewiring of the calcineurin-mediated transcriptional regulatory network.
机译:裂殖酵母粟酒裂殖酵母中钙调神经磷酸酶激活的转录因子Prz1介导对细胞内钙的基因调控。 CrzA和CrzA真菌直系同源基因的全基因组研究已经发现了许多参与保守和物种特异性细胞过程的靶基因。相反,Prz1的靶基因很少公开。本文使用转录组和ChIP芯片分析,在Prz1的诱导条件下,包括CaCl2和衣霉素处理,以及∆pmr1遗传背景,利用转录组和ChIP芯片分析鉴定了广泛的基因。我们鉴定了165个上调的Prz1靶基因,其中大多数在其启动子中都含有钙依赖性反应元件,与酿酒酵母直系同源基因相似。这些基因在功能上丰富了保守的过程,例如细胞壁生物合成。 prz1 + 的过度表达增加了对细胞壁降解酶酶的抗性,这可能是由于O-甘露糖基转移酶编码基因omh1 + 的上调所致。 omh1 + 的丧失消除了该表型。我们发现Prz1絮凝中的新型抑制作用。 prz1 + 的缺失导致组成性絮凝和编码絮凝蛋白Gsf2和Pfl3的基因以及转录因子Cbf12的上调。 gsf2 + 或cbf12 + 的丧失消除了Δprz1菌株的本构絮凝。这项研究表明,Prz1分别作为参与细胞壁生物合成和絮凝的基因的正转录和负转录调节子。此外,/ CrzA和Prz1之间靶基因的比较表明DNA结合特异性有一定的保守性,但钙调神经磷酸酶介导的转录调控网络也有大量的重新连接。

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