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10.7554/eLife.21491 http://scihub22266oqcxt.onion/10.7554/eLife.21491 C5127644!5127644!27852435     free     free     free Deprecated: Implicit conversion from float 225.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 225.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 225.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 225.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       eLife 2016 ; 5 (ä): ä Nephropedia Template TP {{tp|p=27852435|t=2016. SPRTN is a mammalian DNA-binding metalloprotease that resolves DNA-protein crosslinks |pdf=|usr=}}{{27852435}} gab.com Text SPRTN is a mammalian DNA-binding metalloprotease that resolves DNA-protein crosslinks JO: eLife http://www.kidney.de/pget.php?&tw=1&pmid=27852435 #FOAvip Ruijs-Aalfs syndrome is a segmental progeroid syndrome resulting from mutations in the SPRTN gene. Cells derived from patients with SPRTN mutations elicit genomic instability and people afflicted with this syndrome developed hepatocellular carcinoma. Here we describe the molecular mechanism by which SPRTN contributes to genome stability and normal cellular homeostasis. We show that SPRTN is a DNA-dependent mammalian protease required for resolving cytotoxic DNA-protein crosslinks (DPCs)? a function that had only been attributed to the metalloprotease Wss1 in budding yeast. We provide genetic evidence that SPRTN and Wss1 function distinctly in vivo to resolve DPCs. Upon DNA and ubiquitin binding, SPRTN can elicit proteolytic activity; cleaving DPC substrates and itself. SPRTN null cells or cells derived from patients with Ruijs-Aalfs syndrome are impaired in the resolution of covalent DPCs in vivo. Collectively, SPRTN is a mammalian protease required for resolving DNA-protein crosslinks in vivo whose function is compromised in Ruijs-Aalfs syndrome patients.DOI:http://dx.doi.org/10.7554/eLife.21491.001 Twit Text FOAVip SPRTN is a mammalian DNA-binding metalloprotease that resolves DNA-protein crosslinks ????eLife http://www.kidney.de/pget.php?&tw=1&pmid=27852435 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27852435 #FOAvip English Wikipedia <ref>{{Cite pmid|27852435}}</ref> SPRTN is a mammalian DNA-binding metalloprotease that resolves DNA-protein crosslinks #MMPMID27852435 Lopez-Mosqueda J; Maddi K; Prgomet S; Kalayil S; Marinovic-Terzic I; Terzic J; Dikic I eLife 2016[]; 5 (ä): ä PMID27852435show ga Ruijs-Aalfs syndrome is a segmental progeroid syndrome resulting from mutations in the SPRTN gene. Cells derived from patients with SPRTN mutations elicit genomic instability and people afflicted with this syndrome developed hepatocellular carcinoma. Here we describe the molecular mechanism by which SPRTN contributes to genome stability and normal cellular homeostasis. We show that SPRTN is a DNA-dependent mammalian protease required for resolving cytotoxic DNA-protein crosslinks (DPCs)? a function that had only been attributed to the metalloprotease Wss1 in budding yeast. We provide genetic evidence that SPRTN and Wss1 function distinctly in vivo to resolve DPCs. Upon DNA and ubiquitin binding, SPRTN can elicit proteolytic activity; cleaving DPC substrates and itself. SPRTN null cells or cells derived from patients with Ruijs-Aalfs syndrome are impaired in the resolution of covalent DPCs in vivo. Collectively, SPRTN is a mammalian protease required for resolving DNA-protein crosslinks in vivo whose function is compromised in Ruijs-Aalfs syndrome patients.DOI:http://dx.doi.org/10.7554/eLife.21491.001 äSPRTN is a mammalian DNA-binding metalloprotease that resolves DNA-pro(epmc).pdf DeepDyve Pubget Overpricing