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Human DNA helicase IV is nucleolin, an RNA helicase modulated by phosphorylation
Authors:Narendra Tuteja  Ning Wu Huang  Doris Skopac  Renu Tuteja  Sara Hrvatic  Jianwen Zhang  Sandor Pongor  Grard Joseph  Christian Faucher  Franois Amalric  Arturo Falaschi
Affiliation:

a International Centre for Genetic Engineering and Biotechnology, Area Science Park, Padriciano 99, 1-34012, Trieste, Italy

b Centre de Recherche de Biochimie et de Génétique Cellulaires du CNRS, Toulouse, France. Tel. (33-61) 335-859

Abstract:The cDNA encoding human DNA helicase IV (HDH IV), a 100-kDa protein which unwinds DNA in the 5′ to 3′ direction with respect to the bound strand, was cloned and sequenced. It was found to be identical to the human cDNA encoding nucleolin, a ubiquitous eukaryotic protein essential for pre-ribosome assembly. HDH IV/nucleolin can unwind RNA-RNA duplexes, as well as DNA-DNA and DNA-RNA duplexes. Phosphorylation of HDH IV/nucleolin by cdc2 kinase and casein kinase II enhanced its unwinding activity in an additive way. The Gly-rich C-terminal domain possesses a limited ATP-dependent duplex-unwinding activity which contributes to the helicase activity of HDH IV/nucleolin.
Keywords:Unwinding enzyme  cdc2  casein kinase  nucleolus  pre-ribosome assembly
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