4.6 Article

The PPIP5K Family Member Asp1 Controls Inorganic Polyphosphate Metabolism in S. pombe

期刊

JOURNAL OF FUNGI
卷 7, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/jof7080626

关键词

inorganic polyphosphate; phosphate homeostasis; inositol pyrophosphates; Schizosaccharomyces pombe; PPIP5K; Asp1; yeast

资金

  1. Medical Research Council [MR/T028904/1]
  2. Deutsche Forschungsgemeinschaft [FOR1334]
  3. MRC [MR/T028904/1] Funding Source: UKRI

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This study investigated the regulation of polyP metabolism in yeast, revealing that different yeasts utilize different classes of IPPs to regulate polyP synthesis. While the mechanism of polyP synthesis is conserved in yeasts, the regulatory players are diverse.
Inorganic polyphosphate (polyP) which is ubiquitously present in both prokaryotic and eukaryotic cells, consists of up to hundreds of orthophosphate residues linked by phosphoanhydride bonds. The biological role of this polymer is manifold and diverse and in fungi ranges from cell cycle control, phosphate homeostasis and virulence to post-translational protein modification. Control of polyP metabolism has been studied extensively in the budding yeast Saccharomyces cerevisiae. In this yeast, a specific class of inositol pyrophosphates (IPPs), named IP7, made by the IP6K family member Kcs1 regulate polyP synthesis by associating with the SPX domains of the vacuolar transporter chaperone (VTC) complex. To assess if this type of regulation was evolutionarily conserved, we determined the elements regulating polyP generation in the distantly related fission yeast Schizosaccharomyces pombe. Here, the VTC machinery is also essential for polyP generation. However, and in contrast to S. cerevisiae, a different IPP class generated by the bifunctional PPIP5K family member Asp1 control polyP metabolism. The analysis of Asp1 variant S. pombe strains revealed that cellular polyP levels directly correlate with Asp1-made IP8 levels, demonstrating a dose-dependent regulation. Thus, while the mechanism of polyP synthesis in yeasts is conserved, the IPP player regulating polyP metabolism is diverse.

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