DIFFERENT PATHWAYS MEDIATE VIRUS INDUCIBILITY OF THE HUMAN IFN-ALPHA-1 AND IFN-BETA GENES

被引:155
作者
MACDONALD, NJ
KUHL, D
MAGUIRE, D
NAF, D
GALLANT, P
GOSWAMY, A
HUG, H
BUELER, H
CHATURVEDI, M
DELAFUENTE, J
RUFFNER, H
MEYER, F
WEISSMANN, C
机构
[1] Institut für Molekularbiologie I Universität Zürich
关键词
D O I
10.1016/0092-8674(90)90091-R
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
Multimerization of GAAANN generates sequences frequent in virus-inducible promoters. We distinguished different types of (GAAANN)4 sequences mediating virus inducibility. Type I (NN = GT, GC, CT, or CC) responds to IFNs and to IRF-1 and causes silencing. Type II (NN = TG) and type III (NN = CG) neither silence nor respond to IRF-1 or IFN. Type III mediates constitutive transcription and binds the constitutive IEFga factor, whereas type II binds the novel "TG protein‡. IFN-β and IFN-α1 promoters contain different response elements: The former has a type I-like sequence (PRDI) and an NF-κB-binding sequence (PRDII); the latter has a type II-like "TG sequence" and possibly additional elements but does not bind NF-κB. Type I, type II, and NF-κB elements represent three distinct terminal pathways mediating virus induction. © 1990.
引用
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页码:767 / 779
页数:13
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