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10.1371/journal.pgen.1006276

http://scihub22266oqcxt.onion/10.1371/journal.pgen.1006276
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suck abstract from ncbi


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pmid27564576      PLoS+Genet 2016 ; 12 (8): e1006276
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  • Mg2+ Extrusion from Intestinal Epithelia by CNNM Proteins Is Essential for Gonadogenesis via AMPK-TORC1 Signaling in Caenorhabditis elegans #MMPMID27564576
  • Ishii T; Funato Y; Hashizume O; Yamazaki D; Hirata Y; Nishiwaki K; Kono N; Arai H; Miki H
  • PLoS Genet 2016[Aug]; 12 (8): e1006276 PMID27564576show ga
  • Mg2+ serves as an essential cofactor for numerous enzymes and its levels are tightly regulated by various Mg2+ transporters. Here, we analyzed Caenorhabditis elegans strains carrying mutations in genes encoding cyclin M (CNNM) Mg2+ transporters. We isolated inactivating mutants for each of the five Caenorhabditis elegans cnnm family genes, cnnm-1 through cnnm-5. cnnm-1; cnnm-3 double mutant worms showed various phenotypes, among which the sterile phenotype was rescued by supplementing the media with Mg2+. This sterility was caused by a gonadogenesis defect with severely attenuated proliferation of germ cells. Using this gonadogenesis defect as an indicator, we performed genome-wide RNAi screening, to search for genes associated with this phenotype. The results revealed that RNAi-mediated inactivation of several genes restores gonad elongation, including aak-2, which encodes the catalytic subunit of AMP-activated protein kinase (AMPK). We then generated triple mutant worms for cnnm-1; cnnm-3; aak-2 and confirmed that the aak-2 mutation also suppressed the defective gonadal elongation in cnnm-1; cnnm-3 mutant worms. AMPK is activated under low-energy conditions and plays a central role in regulating cellular metabolism to adapt to the energy status of cells. Thus, we provide genetic evidence linking Mg2+ homeostasis to energy metabolism via AMPK.
  • |AMP-Activated Protein Kinases[MESH]
  • |Animals[MESH]
  • |Caenorhabditis elegans Proteins/*genetics/metabolism[MESH]
  • |Caenorhabditis elegans/genetics/growth & development[MESH]
  • |Cation Transport Proteins/*genetics[MESH]
  • |Cyclins/biosynthesis/*genetics[MESH]
  • |Germ Cells/growth & development/metabolism[MESH]
  • |Gonads/growth & development/metabolism[MESH]
  • |Intestinal Mucosa/growth & development/metabolism[MESH]
  • |Longevity/*genetics[MESH]
  • |Magnesium/metabolism[MESH]
  • |Mechanistic Target of Rapamycin Complex 1[MESH]
  • |Multigene Family/genetics[MESH]
  • |Multiprotein Complexes/*genetics[MESH]
  • |Mutation[MESH]
  • |Protein Serine-Threonine Kinases/*genetics/metabolism[MESH]
  • |RNA Interference[MESH]
  • |Signal Transduction/genetics[MESH]


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