TY - JOUR
T1 - Dynamic regulation of the COP9 signalosome in response to DNA damage
AU - Fuzesi-Levi, Maria G.
AU - Ben-Nissan, Gili
AU - Bianchi, Elisabetta
AU - Zhou, Houjiang
AU - Deery, Michael J.
AU - Lilley, Kathryn S.
AU - Levin, Yishai
AU - Sharon, Michal
N1 - Starting Grant from the European Research Council (ERC) [239679]; PRIME-XS Project under the European Community's Seventh Framework Programme [262067]M. S. is grateful for the financial support of a Starting Grant from the European Research Council (ERC) (grant agreement no. 239679) and the PRIME-XS Project (grant agreement no. 262067), both under the European Community's Seventh Framework Programme. M. S. is the incumbent of the Elaine Blond Career Development Chair.
PY - 2014/3
Y1 - 2014/3
N2 - The COP9 signalosome (CSN) is an evolutionarily conserved protein complex that participates in the regulation of the ubiquitin/26S proteasome pathway by controlling the function of cullin-RING-ubiquitin ligases. Impressive progress has been made in deciphering its critical role in diverse cellular and developmental processes. However, little is known about the underlying regulatory principles that coordinate its function. Through biochemical and fluorescence microscopy analyses, we determined that the complex is localized in the cytoplasm, nucleoplasm, and chromatin-bound fractions, each differing in the composition of posttranslationally modified subunits, depending on its location within the cell. During the cell cycle, the segregation between subcellular localizations remains steady. However, upon UV damage, a dose-dependent temporal shuttling of the CSN complex into the nucleus was seen, accompanied by upregulation of specific phosphorylations within CSN1, CSN3, and CSN8. Taken together, our results suggest that the specific spatiotemporal composition of the CSN is highly controlled, enabling the complex to rapidly adapt and respond to DNA damage.
AB - The COP9 signalosome (CSN) is an evolutionarily conserved protein complex that participates in the regulation of the ubiquitin/26S proteasome pathway by controlling the function of cullin-RING-ubiquitin ligases. Impressive progress has been made in deciphering its critical role in diverse cellular and developmental processes. However, little is known about the underlying regulatory principles that coordinate its function. Through biochemical and fluorescence microscopy analyses, we determined that the complex is localized in the cytoplasm, nucleoplasm, and chromatin-bound fractions, each differing in the composition of posttranslationally modified subunits, depending on its location within the cell. During the cell cycle, the segregation between subcellular localizations remains steady. However, upon UV damage, a dose-dependent temporal shuttling of the CSN complex into the nucleus was seen, accompanied by upregulation of specific phosphorylations within CSN1, CSN3, and CSN8. Taken together, our results suggest that the specific spatiotemporal composition of the CSN is highly controlled, enabling the complex to rapidly adapt and respond to DNA damage.
UR - http://www.scopus.com/inward/record.url?scp=84894261696&partnerID=8YFLogxK
U2 - 10.1128/MCB.01598-13
DO - 10.1128/MCB.01598-13
M3 - مقالة
SN - 0270-7306
VL - 34
SP - 1066
EP - 1076
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 6
ER -