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R2TP/Prefoldin-like component RUVBL1/RUVBL2 directly interacts with ZNHIT2 to regulate assembly of U5 small nuclear ribonucleoprotein.
- Source :
-
Nature communications [Nat Commun] 2017 May 31; Vol. 8, pp. 15615. Date of Electronic Publication: 2017 May 31. - Publication Year :
- 2017
-
Abstract
- The R2TP/Prefoldin-like (R2TP/PFDL) complex has emerged as a cochaperone complex involved in the assembly of a number of critical protein complexes including snoRNPs, nuclear RNA polymerases and PIKK-containing complexes. Here we report on the use of multiple target affinity purification coupled to mass spectrometry to identify two additional complexes that interact with R2TP/PFDL: the TSC1-TSC2 complex and the U5 small nuclear ribonucleoprotein (snRNP). The interaction between R2TP/PFDL and the U5 snRNP is mostly mediated by the previously uncharacterized factor ZNHIT2. A more general function for the zinc-finger HIT domain in binding RUVBL2 is exposed. Disruption of ZNHIT2 and RUVBL2 expression impacts the protein composition of the U5 snRNP suggesting a function for these proteins in promoting the assembly of the ribonucleoprotein. A possible implication of R2TP/PFDL as a major effector of stress-, energy- and nutrient-sensing pathways that regulate anabolic processes through the regulation of its chaperoning activity is discussed.
- Subjects :
- ATPases Associated with Diverse Cellular Activities genetics
Alternative Splicing genetics
Carrier Proteins genetics
Cell Line
DNA Helicases genetics
Energy Metabolism genetics
HEK293 Cells
HeLa Cells
Humans
Phosphoproteins genetics
RNA, Small Interfering genetics
TOR Serine-Threonine Kinases metabolism
Tuberous Sclerosis Complex 1 Protein
Tuberous Sclerosis Complex 2 Protein
ATPases Associated with Diverse Cellular Activities metabolism
Carrier Proteins metabolism
DNA Helicases metabolism
Phosphoproteins metabolism
Ribonucleoprotein, U5 Small Nuclear biosynthesis
Tumor Suppressor Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 28561026
- Full Text :
- https://doi.org/10.1038/ncomms15615