SART3-Dependent Accumulation of Incomplete Spliceosomal snRNPs in Cajal Bodies
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
25600876
DOI
10.1016/j.celrep.2014.12.030
PII: S2211-1247(14)01059-6
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Cajal bodies (CBs) are evolutionarily conserved nuclear structures involved in the metabolism of spliceosomal small nuclear ribonucleoprotein particles (snRNPs). CBs are not present in all cell types, and the trigger for their formation is not yet known. Here, we depleted cells of factors required for the final steps of snRNP assembly and assayed for the presence of stalled intermediates in CBs. We show that depletion induces formation of CBs in cells that normally lack these nuclear compartments, suggesting that CB nucleation is triggered by an imbalance in snRNP assembly. Accumulation of stalled intermediates in CBs depends on the di-snRNP assembly factor SART3. SART3 is required for both the induction of CB formation as well as the tethering of incomplete snRNPs to coilin, the CB scaffolding protein. We propose a model wherein SART3 monitors tri-snRNP assembly and sequesters incomplete particles in CBs, thereby allowing cells to maintain a homeostatic balance of mature snRNPs in the nucleoplasm.
Citace poskytuje Crossref.org
Dynamic interaction of spliceosomal snRNPs with coilin explains Cajal body characteristics
The SMN complex drives structural changes in human snRNAs to enable snRNP assembly
TSSC4 is a component of U5 snRNP that promotes tri-snRNP formation
DIS3L2 and LSm proteins are involved in the surveillance of Sm ring-deficient snRNAs
Assembly of the U5 snRNP component PRPF8 is controlled by the HSP90/R2TP chaperones
Cajal bodies and snRNPs - friends with benefits
Mutations in spliceosomal proteins and retina degeneration