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10.1016/j.bbamcr.2016.03.021

http://scihub22266oqcxt.onion/10.1016/j.bbamcr.2016.03.021
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C4886714!4886714!27033521
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suck abstract from ncbi


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pmid27033521      Biochim+Biophys+Acta 2016 ; 1863 (6 Pt A): 1307-18
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  • Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation #MMPMID27033521
  • Kim JH; Ki SM; Joung JG; Scott E; Heynen-Genel S; Aza-Blanc P; Kwon CH; Kim J; Gleeson JG; Lee JE
  • Biochim Biophys Acta 2016[Jun]; 1863 (6 Pt A): 1307-18 PMID27033521show ga
  • Biogenesis of the primary cilium, a cellular organelle mediating various signaling pathways, is generally coordinated with cell cycle exit/re-entry. Although the dynamic cell cycle-associated profile of the primary cilium has been largely accepted, the mechanism governing the link between ciliogenesis and cell cycle progression has been poorly understood. Using a human genome-wide RNAi screen, we identify genes encoding subunits of the spliceosome and proteasome as novel regulators of ciliogenesis. We demonstrate that 1) the mRNA processing-related hits are essential for RNA expression of molecules acting in cilia disassembly, such as AURKA and PLK1, and 2) the ubiquitin-proteasome systems (UPS)-involved hits are necessary for proteolysis of molecules acting in cilia assembly, such as IFT88 and CPAP. In particular, we show that these screen hit-associated mechanisms are crucial for both cilia assembly and cell cycle arrest in response to serum withdrawal. Finally, our data suggest that the mRNA processing mechanism may modulate the UPS-dependent decay of cilia assembly regulators to control ciliary resorption-coupled cell cycle re-entry.
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