A cellular cofactor for the constitutive transport element of type D retrovirus

被引:128
作者
Tang, HL
Gaietta, GM
Fischer, WH
Ellisman, MH
WongStaal, F
机构
[1] UNIV CALIF SAN DIEGO,DEPT MED & BIOL,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,DEPT BIOL,LA JOLLA,CA 92093
[3] UNIV CALIF SAN DIEGO,DEPT NEUROSCI,LA JOLLA,CA 92093
[4] UNIV CALIF SAN DIEGO,SAN DIEGO MICROSCOPY IMAGING RESOURCE,LA JOLLA,CA 92093
[5] SALK INST BIOL STUDIES,CLAYTON FDN LABS PEPTIDE BIOL,LA JOLLA,CA 92097
关键词
HELA-CELLS; RNA; INHIBITION; CYTOPLASM; NUCLEUS;
D O I
10.1126/science.276.5317.1412
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A human nuclear protein that specifically interacts with the constitutive transport element (CTE) of simian retrovirus was identified as adenosine 5'-triphosphate-dependent RNA helicase A. This protein could bind to functional CTE but not to inactive CTE mutants. The interaction of helicase A with CTE was distinct from previously described helicase activity of this protein. Helicase A shuttled from the nucleus to the cytoplasm in the presence of a transcription inhibitor or in cells transiently overexpressing CTE-containing RNA. In vivo colocalization of helicase A and CTE was observed in experiments that combined in situ hybridization and immunostaining, These results suggest that helicase A plays a role in the nuclear export of CTE-containing RNA.
引用
收藏
页码:1412 / 1415
页数:4
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