TY - JOUR
T1 - Active regulator of SIRT1 is required for ribosome biogenesis and function
AU - Knight, John R.P.
AU - Willis, Anne E.
AU - Milner, Jo
N1 - Funding Information:
Yorkshire Cancer Research (to J.M.); Medical Research Council and Biotechnology and Biological Sciences Research Council (to A.E.W.). Funding for open access charge: Medical Research Council.
PY - 2013/4
Y1 - 2013/4
N2 - Active regulator of SIRT1 (AROS) binds and upregulates SIRT1, an NAD +-dependent deacetylase. In addition, AROS binds RPS19, a structural ribosomal protein, which also functions in ribosome biogenesis and is implicated in multiple disease states. The significance of AROS in relation to ribosome biogenesis and function is unknown. Using human cells, we now show that AROS localizes to (i) the nucleolus and (ii) cytoplasmic ribosomes. Co-localization with nucleolar proteins was verified by confocal immunofluorescence of endogenous protein and confirmed by AROS depletion using RNAi. AROS association with cytoplasmic ribosomes was analysed by sucrose density fractionation and immunoprecipitation, revealing that AROS selectively associates with 40S ribosomal subunits and also with polysomes. RNAi-mediated depletion of AROS leads to deficient ribosome biogenesis with aberrant precursor ribosomal RNA processing, reduced 40S subunit ribosomal RNA and 40S ribosomal proteins (including RPS19). Together, this results in a reduction in 40S subunits and translating polysomes, correlating with reduced overall cellular protein synthesis. Interestingly, knockdown of AROS also results in a functionally significant increase in eIF2α phosphorylation. Overall, our results identify AROS as a factor with a role in both ribosome biogenesis and ribosomal function.
AB - Active regulator of SIRT1 (AROS) binds and upregulates SIRT1, an NAD +-dependent deacetylase. In addition, AROS binds RPS19, a structural ribosomal protein, which also functions in ribosome biogenesis and is implicated in multiple disease states. The significance of AROS in relation to ribosome biogenesis and function is unknown. Using human cells, we now show that AROS localizes to (i) the nucleolus and (ii) cytoplasmic ribosomes. Co-localization with nucleolar proteins was verified by confocal immunofluorescence of endogenous protein and confirmed by AROS depletion using RNAi. AROS association with cytoplasmic ribosomes was analysed by sucrose density fractionation and immunoprecipitation, revealing that AROS selectively associates with 40S ribosomal subunits and also with polysomes. RNAi-mediated depletion of AROS leads to deficient ribosome biogenesis with aberrant precursor ribosomal RNA processing, reduced 40S subunit ribosomal RNA and 40S ribosomal proteins (including RPS19). Together, this results in a reduction in 40S subunits and translating polysomes, correlating with reduced overall cellular protein synthesis. Interestingly, knockdown of AROS also results in a functionally significant increase in eIF2α phosphorylation. Overall, our results identify AROS as a factor with a role in both ribosome biogenesis and ribosomal function.
UR - http://www.scopus.com/inward/record.url?scp=84876521221&partnerID=8YFLogxK
U2 - 10.1093/nar/gkt129
DO - 10.1093/nar/gkt129
M3 - Article
C2 - 23462953
AN - SCOPUS:84876521221
SN - 0305-1048
VL - 41
SP - 4185
EP - 4197
JO - Nucleic acids research
JF - Nucleic acids research
IS - 7
ER -