REVERSAL OF CREATINE-KINASE TRANSLATIONAL REPRESSION BY 3' UNTRANSLATED SEQUENCES

被引:65
作者
CHNG, JLC
SHOEMAKER, DL
SCHIMMEL, P
HOLMES, EW
机构
[1] DUKE UNIV,DEPT MED,DURHAM,NC 27710
[2] DUKE UNIV,DEPT BIOCHEM,DURHAM,NC 27710
[3] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
关键词
D O I
10.1126/science.2343304
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 subline of U937 cells (U937D) was obtained in which creatine kinase B (CK-B) messenger RNA was present and bound to ribosomes, but CK activity was undetectable. Transformation of U937D cells with retrovirus vectors that contain the 3′ untranslated region (3′ UTR) of CK-B messenger RNA exhibited CK activity with no change in abundance of CK-B mRNA. The 3′ UTR formed a complex in vitro with a component of S100 extracts from wild-type cells. This binding activity was not detectable in S100 extracts from cells that expressed CK activity after transformation with the 3′ UTR-containing vector. These results suggest that translation of CK-B is repressed by binding of a soluble factor or factors to the 3′ UTK.
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收藏
页码:1003 / 1006
页数:4
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