Henry Theresa C, Power Juliette E, Kerwin Christine L, Mohammed Aishat, Weissman Jonathan S, Cameron Dale M, Wykoff Dennis D
Department of Biology, Villanova University, 800 Lancaster Ave., Villanova, PA 19085, USA.
Eukaryot Cell. 2011 Feb;10(2):198-206. doi: 10.1128/EC.00216-10. Epub 2010 Dec 17.
The phosphate signal transduction (PHO) pathway, which regulates genes in response to phosphate starvation, is well defined in Saccharomyces cerevisiae. We asked whether the PHO pathway was the same in the distantly related fission yeast Schizosaccharomyces pombe. We screened a deletion collection for mutants aberrant in phosphatase activity, which is primarily a consequence of pho1(+) transcription. We identified a novel zinc finger-containing protein (encoded by spbc27b12.11c(+)), which we have named pho7(+), that is essential for pho1(+) transcriptional induction during phosphate starvation. Few of the S. cerevisiae genes involved in the PHO pathway appear to be involved in the regulation of the phosphate starvation response in S. pombe. Only the most upstream genes in the PHO pathway in S. cerevisiae (ADO1, DDP1, and PPN1) share a similar role in both yeasts. Because ADO1 and DDP1 regulate ATP and IP(7) levels, we hypothesize that the ancestor of these yeasts must have sensed similar metabolites in response to phosphate starvation but have evolved distinct mechanisms in parallel to sense these metabolites and induce phosphate starvation genes.
磷酸信号转导(PHO)途径可响应磷酸盐饥饿调节基因,在酿酒酵母中已得到充分阐明。我们研究了在亲缘关系较远的裂殖酵母粟酒裂殖酵母中PHO途径是否相同。我们筛选了一个缺失文库,寻找磷酸酶活性异常的突变体,磷酸酶活性异常主要是pho1(+)转录的结果。我们鉴定出一种新型含锌指蛋白(由spbc27b12.11c(+)编码),我们将其命名为pho7(+),它在磷酸盐饥饿期间对pho1(+)转录诱导至关重要。参与酿酒酵母PHO途径的基因中,似乎很少有参与粟酒裂殖酵母磷酸盐饥饿反应调控的。只有酿酒酵母PHO途径中最上游的基因(ADO1、DDP1和PPN1)在两种酵母中发挥类似作用。由于ADO1和DDP1调节ATP和IP(7)水平,我们推测这些酵母的祖先在响应磷酸盐饥饿时一定感知到了类似的代谢物,但已平行进化出不同机制来感知这些代谢物并诱导磷酸盐饥饿基因。