Patterns of coordinate down-regulation of ARE-containing transcripts following immune cell activation

被引:47
作者
Raghavan, A
Dhalla, M
Bakheet, T
Ogilvie, RL
Vlasova, IA
Khabar, KSA
Williams, BRG
Bohjanen, PR
机构
[1] Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA
[2] King Faisal Specialist Hosp & Res Ctr, Dept Biol & Med Res, Riyadh, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Bioinformat Sect, Riyadh, Saudi Arabia
[4] Cleveland Clin, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44106 USA
[5] Univ Minnesota, Dept Med, Div Infect Dis, Minneapolis, MN 55455 USA
[6] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
关键词
D O I
10.1016/j.ygeno.2004.08.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We evaluated the expression of over 900 AU-rich element (ARE)-containing transcripts in primary human T lymphocytes following stimulation with anti-CD3 and anti-CD28 antibodies and found that approximately 48% of these transcripts were regulated following T cell activation. We identified approximately 145 ARE-containing transcripts that were rapidly induced and then rapidly disappeared within I h after activation. Another 250 ARE-containing transcripts expressed in resting T cells were rapidly turned off within 30 min after activation. The rates of transcript disappearance correlated well with rapid mRNA decay measured following transcriptional arrest with actinomycin D. We identified a subset of ARE-containing transcripts that were rapidly induced following T cell activation that were also induced following lipopolysaccharide stimulation of THP-1 monocytes, and these transcripts exhibited rapid decay in both cell types. Our results suggest that ARE-mediated mRNA decay plays an important role in the precisely coordinated down-regulation of gene expression following immune cell activation. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1002 / 1013
页数:12
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