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PROMOTER CONTROL OF TRANSLATION IN XENOPUS OOCYTES
被引:22
作者:
GUNKEL, N
BRADDOCK, M
THORBURN, AM
MUCKENTHALER, M
KINGSMAN, AJ
KINGSMAN, SM
机构:
[1] EUROPEAN MOLEC BIOL LAB, W-6900 HEIDELBERG, GERMANY
[2] UNIV OXFORD, DEPT BIOCHEM, RETROVIRUS MOLEC BIOL GRP, OXFORD OX1 3QU, ENGLAND
[3] UNIV UTAH, INST HUMAN GENET, DEPT CARDIOL, SALT LAKE CITY, UT USA
关键词:
D O I:
10.1093/nar/23.3.405
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The HIV-1 promoter directs the high level production of transcripts in Xenopus oocytes. However, despite being exported to the cytoplasm, the transcripts are not translated [M. Braddock, A. M. Thorburn, A. Chambers, G. D. Elliott, G. J. Anderson, A. J. Kingsman and S. M. Kingsman (1990) Cell, 62, 1123-1133]. We have shown previously that this is a function of promoter sequences and is independent of the TAR RNA element that is normally located at the 5' end of ail HIV mRNAs. We now show that a three nucleotide substitution at position -340, upstream of the RNA start site, reverses the translation inhibition. This site coincides with a sequence that can bind the haematopoietic transcription factor GATA. The inhibition of translation can also be reversed by treatment with inhibitors of casein kinase II or by injection into the nucleus of antibodies specific for the FRGY2 family of RNP proteins. We suggest that the -340 site influences the quality of the transcription complex such that transcripts are diverted to a nucleus-dependent translation inhibition pathway.
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页码:405 / 412
页数:8
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