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Developmental stage-dependent metabolic regulation during meiotic differentiation in budding yeast

Overview of attention for article published in BMC Biology, September 2014
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Title
Developmental stage-dependent metabolic regulation during meiotic differentiation in budding yeast
Published in
BMC Biology, September 2014
DOI 10.1186/s12915-014-0060-x
Pubmed ID
Authors

Thomas Walther, Fabien Létisse, Lindsay Peyriga, Ceren Alkim, Yuchen Liu, Aurélie Lardenois, Hélène Martin-Yken, Jean-Charles Portais, Michael Primig, Jean Marie François\

Abstract

BackgroundThe meiotic developmental pathway in yeast enables both differentiation of vegetative cells into haploid spores that ensure long-term survival, and recombination of the parental DNA to create genetic diversity. Despite the importance of proper metabolic regulation for the supply of building blocks and energy, little is known about the reprogramming of central metabolic pathways in meiotically differentiating cells during passage through successive developmental stages.ResultsMetabolic regulation during meiotic differentiation in budding yeast was analysed by integrating information on genome-wide transcriptional activity, 26 enzymatic activities in the central metabolism, the dynamics of 67 metabolites, and a metabolic flux analysis at mid-stage meiosis. Analyses of mutants arresting sporulation at defined stages demonstrated that metabolic reprogramming is tightly controlled by the progression through the developmental pathway. The correlation between transcript levels and enzymatic activities in the central metabolism varies significantly in a developmental-stage dependent manner. The complete loss of phosphofructokinase activity at mid-stage meiosis enables a unique setup of the glycolytic pathway which facilitates carbon flux repartitioning into synthesis of spore-wall precursors during the co-assimilation of glycogen and acetate. The need for correct homeostasis of purine nucleotides during the meiotic differentiation was demonstrated by the sporulation defect of the AMP deaminase mutant, amd1, which exhibited hyper-accumulation of ATP accompanied by depletion of guanosine nucleotides.ConclusionsOur systems-level analysis shows that reprogramming of the central metabolism during the meiotic differentiation is controlled at different hierarchical levels to meet the metabolic and energetic needs at successive developmental stages.

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The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Slovakia 1 3%
Unknown 34 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 12 34%
Researcher 10 29%
Other 3 9%
Student > Master 3 9%
Unspecified 2 6%
Other 2 6%
Unknown 3 9%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 14 40%
Agricultural and Biological Sciences 13 37%
Unspecified 2 6%
Business, Management and Accounting 1 3%
Immunology and Microbiology 1 3%
Other 0 0%
Unknown 4 11%