4.6 Article

Time-dependent regulation analysis dissects shifts between metabolic and gene-expression regulation during nitrogen starvation in baker's yeast

期刊

FEBS JOURNAL
卷 276, 期 19, 页码 5521-5536

出版社

WILEY
DOI: 10.1111/j.1742-4658.2009.07235.x

关键词

fermentative capacity; glycolysis; regulation analysis; Saccharomyces cerevisiae; systems biology

资金

  1. IOP Genomics program of Senter Novem
  2. STW
  3. NGI-Kluyver Centre
  4. NWO-SysMO
  5. BBSRC
  6. EPSRC
  7. AstraZeneca
  8. EU
  9. NucSys
  10. ECMOAN
  11. UniCellSys
  12. Biotechnology and Biological Sciences Research Council [BB/D019079/1, BB/C008219/1] Funding Source: researchfish
  13. BBSRC [BB/D019079/1] Funding Source: UKRI

向作者/读者索取更多资源

Time-dependent regulation analysis is a new methodology that allows us to unravel, both quantitatively and dynamically, how and when functional changes in the cell are brought about by the interplay of gene expression and metabolism. In this first experimental implementation, we dissect the initial and late response of baker's yeast upon a switch from glucose-limited growth to nitrogen starvation. During nitrogen starvation, unspecific bulk degradation of cytosolic proteins and small organelles (autophagy) occurs. If this is the primary cause of loss of glycolytic capacity, one would expect the cells to regulate their glycolytic capacity through decreasing simultaneously and proportionally the capacities of the enzymes in the first hour of nitrogen starvation. This should lead to regulation of the flux which is initially dominated by changes in the enzyme capacity. However, metabolic regulation is also known to act fast. To analyse the interplay between autophagy and metabolism, we examined the first 4 h of nitrogen starvation in detail using time-dependent regulation analysis. Some enzymes were initially regulated more by a breakdown of enzyme capacity and only later through metabolic regulation. However, other enzymes were regulated metabolically in the first hours and then shifted towards regulation via enzyme capacity. We conclude that even initial regulation is subtle and governed by different molecular levels.

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