| Literature DB >> 25514182 |
Martin Machyna1, Stephanie Kehr2, Korinna Straube1, Dennis Kappei3, Frank Buchholz3, Falk Butter4, Jernej Ule5, Jana Hertel2, Peter F Stadler2, Karla M Neugebauer6.
Abstract
Coilin protein scaffolds Cajal bodies (CBs)-subnuclear compartments enriched in small nuclear RNAs (snRNAs)-and promotes efficient spliceosomal snRNP assembly. The molecular function of coilin, which is intrinsically disordered with no defined motifs, is poorly understood. We use UV crosslinking and immunoprecipitation (iCLIP) to determine whether mammalian coilin binds RNA in vivo and to identify targets. Robust detection of snRNA transcripts correlated with coilin ChIP-seq peaks on snRNA genes, indicating that coilin binding to nascent snRNAs is a site-specific CB nucleator. Surprisingly, several hundred small nucleolar RNAs (snoRNAs) were identified as coilin interactors, including numerous unannotated mouse and human snoRNAs. We show that all classes of snoRNAs concentrate in CBs. Moreover, snoRNAs lacking specific CB retention signals traffic through CBs en route to nucleoli, consistent with the role of CBs in small RNP assembly. Thus, coilin couples snRNA and snoRNA biogenesis, making CBs the cellular hub of small ncRNA metabolism.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25514182 DOI: 10.1016/j.molcel.2014.10.004
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970