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Repression of ADH1 and ADH3 during zinc deficiency by Zap1-induced intergenic RNA transcripts
被引:90
作者:
Bird, Amanda J.
Gordon, Mat
Eide, David J.
Winge, Dennis R.
机构:
[1] Univ Utah, Hlth Sci Ctr, Dept Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Hlth Sci Ctr, Dept Biochem, Salt Lake City, UT 84132 USA
[3] Univ Utah, Sch Med, Huntsman Canc Inst, Salt Lake City, UT USA
[4] Univ Wisconsin, Dept Nutrit Sci, Madison, WI USA
关键词:
gene repression;
metalloregulation;
non-coding RNA;
Zap1;
zinc;
D O I:
10.1038/sj.emboj.7601453
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 transcriptional activator Zap1 induces target gene expression in response to zinc deficiency. We demonstrate that during zinc starvation, Zap1 is required for the repression of ADH1 expression. ADH1 encodes the major zinc-dependent alcohol dehydrogenase that is utilized during fermentation. During zinc starvation, Zap1 binds upstream of the activator Rap1 and induces an intergenic RNA transcript, ZRR1. ZRR1 expression leads to the transient displacement of Rap1 from the ADH1 promoter resulting in ADH1 repression. Using a microarray-based approach, we screened for additional genes repressed by Zap1 intergenic transcripts. We found that ADH3, the major mitochondrial alcohol dehydrogenase, is regulated in a manner similar to ADH1. Thus, during zinc deficiency, Zap1 mediates the repression of two of the most abundant zinc-requiring enzymes.
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页码:5726 / 5734
页数:9
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