Nucleocapsid phosphorylation and RNA helicase DDX1 recruitment enables coronavirus transition from discontinuous to continuous transcription

Cell Host and Microbe

Volumn 16, Issue 4, 2014, Pages 462-472

  Wu, Chia Hsin ^a   Chen, Pei Jer ^a,b   Yeh, Shiou Hwei ^a,b,c  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CORONAVIRUS;

DDX1 PROTEIN, MOUSE; DEAD BOX PROTEIN; GLYCOGEN SYNTHASE KINASE 3; MESSENGER RNA; NUCLEOCAPSID PROTEIN; NUCLEOCAPSID PROTEIN, CORONAVIRUS; PROTEIN BINDING; RNA HELICASE; VIRUS RNA;

ANIMAL; BIOSYNTHESIS; CELL LINE; CORONAVIRIDAE; GENETIC TRANSCRIPTION; HOST PATHOGEN INTERACTION; METABOLISM; MOUSE; PHOSPHORYLATION; PHYSIOLOGY; PROTEIN PROCESSING;

ANIMALS; CELL LINE; CORONAVIRUS; DEAD-BOX RNA HELICASES; GLYCOGEN SYNTHASE KINASE 3; HOST-PATHOGEN INTERACTIONS; MICE; NUCLEOCAPSID PROTEINS; PHOSPHORYLATION; PROTEIN BINDING; PROTEIN PROCESSING, POST-TRANSLATIONAL; RNA HELICASES; RNA, MESSENGER; RNA, VIRAL; TRANSCRIPTION, GENETIC;

EID: 84908060960     PISSN: 19313128     EISSN: 19346069     Source Type: Journal    
DOI: 10.1016/j.chom.2014.09.009     Document Type: Article

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