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10.1038/ncomms13508

http://scihub22266oqcxt.onion/10.1038/ncomms13508
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C5473638!5473638 !27869116
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suck abstract from ncbi


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pmid27869116
      Nat+Commun 2016 ; 7 (ä): 13508
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  • Autophagy controls centrosome number by degrading Cep63 #MMPMID27869116
  • Watanabe Y ; Honda S ; Konishi A ; Arakawa S ; Murohashi M ; Yamaguchi H ; Torii S ; Tanabe M ; Tanaka S ; Warabi E ; Shimizu S
  • Nat Commun 2016[Nov]; 7 (ä): 13508 PMID27869116 show ga
  • Centrosome number is associated with the chromosome segregation and genomic stability. The ubiquitin-proteasome system is considered to be the main regulator of centrosome number. However, here we show that autophagy also regulates the number of centrosomes. Autophagy-deficient cells carry extra centrosomes. The autophagic regulation of centrosome number is dependent on a centrosomal protein of 63 (Cep63) given that cells lacking autophagy contain multiple Cep63 dots that are engulfed and digested by autophagy in wild-type cells, and that the upregulation of Cep63 increases centrosome number. Cep63 is recruited to autophagosomes via interaction with p62, a molecule crucial for selective autophagy. In vivo, hematopoietic cells from autophagy-deficient and p62(-/-) mice also contained multiple centrosomes. These results indicate that autophagy controls centrosome number by degrading Cep63.
  • |*Autophagy [MESH]
  • |*Centrosome [MESH]
  • |Animals [MESH]
  • |Autophagy-Related Protein 5/metabolism [MESH]
  • |Autophagy-Related Protein 7/genetics/metabolism [MESH]
  • |Cell Cycle Proteins/genetics/*metabolism [MESH]
  • |Cells, Cultured [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Mice, Knockout [MESH]
  • |Neoplasm Proteins/genetics/*metabolism [MESH]


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