https://transhumanist.ru/index.php?action=history&feed=atom&title=CAMKK2 2026-04-07T15:01:31Z История изменений этой страницы в вики MediaWiki 1.43.6 https://transhumanist.ru/index.php?title=CAMKK2&diff=6035&oldid=prev 2021-05-12T15:07:53Z

<p>Новая страница: «Calcium/calmodulin-dependent protein kinase kinase 2 (EC 2.7.11.17) (CaM-KK 2) (CaM-kinase kinase 2) (CaMKK 2) (Calcium/calmodulin-dependent protein kinase kinase...»</p> <p><b>Новая страница</b></p><div>Calcium/calmodulin-dependent protein kinase kinase 2 (EC 2.7.11.17) (CaM-KK 2) (CaM-kinase kinase 2) (CaMKK 2) (Calcium/calmodulin-dependent protein kinase kinase beta) (CaM-KK beta) (CaM-kinase kinase beta) (CaMKK beta) [CAMKKB] [KIAA0787]<br /> <br /> ==Publications==<br /> <br /> {{medline-entry<br /> |title=The GID ubiquitin ligase complex is a regulator of AMPK activity and organismal lifespan.<br /> |pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31795790<br /> |abstract=The AMP-activated protein kinase (AMPK) regulates cellular energy homeostasis by sensing the metabolic status of the cell. AMPK is regulated by phosphorylation and dephosphorylation as a result of changing AMP/ATP levels and by removal of inhibitory ubiquitin residues by [[USP10]]. In this context, we identified the GID-complex, an evolutionarily conserved ubiquitin-ligase-complex (E3), as a negative regulator of AMPK activity. Our data show that the GID-complex targets AMPK for ubiquitination thereby altering its activity. Cells depleted of GID-subunits mimic a state of starvation as shown by increased AMPK activity and macroautophagic/autophagic flux as well as reduced [[MTOR]] activation. Consistently, [i]gid[/i]-genes knockdown in [i]C. elegans[/i] results in increased organismal lifespan. This study may contribute to understand metabolic disorders such as type 2 diabetes mellitus and morbid obesity and implements alternative therapeutic approaches to alter AMPK activity. ACTB: actin, beta; ADP: adenosine diphosphate; AMP: adenosine monophosphate; AMPK: AMP-activated protein kinase; ARMC8: armadillo repeat containing 8; ATP: adenosine triphosphate; BafA1: bafilomycin A ; BCAA: branched chain amino acid; BICC1: BicC family RNA binding protein 1; BSA: bovine serum albumin; [[CAMKK2]] kinase: calcium/calmodulin dependent protein kinase kinase 2, beta; CHX: cycloheximide; DMEM: Dulbecco&#039;s modified Eagle&#039;s medium; E1: ubiquitin-activating enzyme; E2: ubiquitin-conjugating enzyme; E3: ubiquitin ligase; ECAR: extracellular acidification rate; FACS: fluorescent associated cell sorter; FBP1: fructose-bisphosphatase 1; FCCP: carbonyl cyanide-4 (trifluoromethoxy) phenylhydrazone; G6P: glucose-6-phosphate; GDP: guanosine diphosphate; GFP: green fluorescent protein; GID: glucose induced degradation deficient; GMP: guanosine monophosphate; GTP: guanosine triphosphate; HBP1: high mobility group box transcription factor 1; HPRT: hypoxanthine guanine phosphoribosyl transferase; KO: knock out; LE: long exposure; MAEA: macrophage erythroblast attacher; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MKLN1: muskelin 1; mRNA: messenger RNA; [[MTOR]]: mechanistic target of rapamycin; NES: normalized enrichment score; OCR: oxygen consumption rate; PBS: phosphate buffered saline; PCK1: phosphoenolpyruvate carboxykinase 1, cytosolic; PCR: polymerase chain reaction; PFA: paraformaldehyde; [[RAN]]BP9: [[RAN]] binding protein 9; RING: really interesting new gene; RMND5: required for meiotic nuclear division5 homolog; RPS6: ribosomal protein S6; RPTOR: regulatory associated protein of [[MTOR]], complex 1; SE: short exposure; SEM: standard error of the mean; SQSTM1/p62: sequestosome 1; TSC2: tuberous sclerosis complex 2; TUBA4A: tubulin; TUBE: tandem ubiquitin binding entities; Ub: ubiquitin; UPS: ubiquitin proteasome system; WDR26: WD repeat domain 26; WT: wild type.<br /> <br /> |keywords=* AMPK<br /> * GID<br /> * autophagy<br /> * longevity<br /> * primary cilium<br /> * ubiquitination<br /> |full-text-url=https://sci-hub.do/10.1080/15548627.2019.1695399<br /> }}</div>

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