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Description
  • Nutrient sensing and metabolic reprogramming are crucial for metazoan cell aging and tumor growth. Here, we identify metabolic and regulatory parallels between a layered, multicellular yeast colony and a tumor-affected organism. During development, a yeast colony stratifies into U and L cells occupying the upper and lower colony regions, respectively. U cells activate a unique metabolism controlled by the glutamine-induced TOR pathway, amino acid sensing systems (SPS and Gcn4p) and signaling from mitochondria with lowered respiration. These systems jointly modulate U cell physiology, which adapts to nutrient limitations and utilize the nutrients released from L cells. Stress-resistant U cells share metabolic pathways and other similar characteristics with tumor cells, including the ability to proliferate. L cells behave similarly to stressed and starving cells, which activate degradative mechanisms to provide nutrients to U cells. Our data suggest a nutrient flow between both cell types, resembling the Cori cycle and glutamine-NH4 + shuttle between tumor and healthy metazoan cells.
  • Nutrient sensing and metabolic reprogramming are crucial for metazoan cell aging and tumor growth. Here, we identify metabolic and regulatory parallels between a layered, multicellular yeast colony and a tumor-affected organism. During development, a yeast colony stratifies into U and L cells occupying the upper and lower colony regions, respectively. U cells activate a unique metabolism controlled by the glutamine-induced TOR pathway, amino acid sensing systems (SPS and Gcn4p) and signaling from mitochondria with lowered respiration. These systems jointly modulate U cell physiology, which adapts to nutrient limitations and utilize the nutrients released from L cells. Stress-resistant U cells share metabolic pathways and other similar characteristics with tumor cells, including the ability to proliferate. L cells behave similarly to stressed and starving cells, which activate degradative mechanisms to provide nutrients to U cells. Our data suggest a nutrient flow between both cell types, resembling the Cori cycle and glutamine-NH4 + shuttle between tumor and healthy metazoan cells. (en)
Title
  • Cell Differentiation within a Yeast Colony: Metabolic and Regulatory Parallels with a Tumor-Affected Organism
  • Cell Differentiation within a Yeast Colony: Metabolic and Regulatory Parallels with a Tumor-Affected Organism (en)
skos:prefLabel
  • Cell Differentiation within a Yeast Colony: Metabolic and Regulatory Parallels with a Tumor-Affected Organism
  • Cell Differentiation within a Yeast Colony: Metabolic and Regulatory Parallels with a Tumor-Affected Organism (en)
skos:notation
  • RIV/00216208:11310/12:10120765!RIV13-GA0-11310___
http://linked.open...avai/riv/aktivita
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  • I, P(GA204/08/0718), P(LC531), Z(MSM0021620858)
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  • 4
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  • 126223
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  • RIV/00216208:11310/12:10120765
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  • amino acid sensing systems; TOR pathway; U and L cells; yeast colony; metabolic reprogramming; nutrient sensing (en)
http://linked.open.../riv/klicoveSlovo
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  • US - Spojené státy americké
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  • [97F096800C7E]
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  • Molecular Cell
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  • 46
http://linked.open...iv/tvurceVysledku
  • Váchová, Libuše
  • Čáp, Michal
  • Palková, Zdena
  • Harant, Karel
  • Štěpánek, Luděk
http://linked.open...ain/vavai/riv/wos
  • 000304518900008
http://linked.open...n/vavai/riv/zamer
issn
  • 1097-2765
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.molcel.2012.04.001
http://localhost/t...ganizacniJednotka
  • 11310
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