Identification and functional outcome of mRNAs associated with RNA-binding protein TIA-1

被引:196
作者
de Silanes, IL
Galbán, S
Martindale, JL
Yang, XL
Mazan-Mamczarz, K
Indig, FE
Falco, G
Zhan, M
Gorospe, M
机构
[1] NIA, IRP, LCMB, NIH, Baltimore, MD 21224 USA
[2] NIA, IRP, Res Resources Branch, NIH, Baltimore, MD 21224 USA
[3] NIA, IRP, Genet Lab, NIH, Baltimore, MD 21224 USA
关键词
D O I
10.1128/MCB.25.21.9520-9531.2005
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 RNA-binding protein TIA-1 (T-cell intracellular antigen 1) functions as a posttranscriptional regulator of gene expression and aggregates to form stress granules following cellular damage. TIA-1 was previously shown to bind mRNAs encoding tumor necrosis factor alpha (TNF-alpha) and cyclooxygenase 2 (COX-2), but TIA-1 target mRNAs have not been systematically identified. Here, immunoprecipitation (IP) of TIA-1-RNA complexes, followed by microarray-based identification and computational analysis of bound transcripts, was used to elucidate a common motif present among TIA-1 target mRNAs. The predicted TIA-1 motif was a U-rich, 30- to 37-nucleotide (nt)-long bipartite element forming loops of variable size and a bent stem. The TIA-1 motif was found in the TNF-alpha and COX-2 mRNAs and in 3,019 additional UniGene transcripts (similar to 3% of the UniGene database), localizing preferentially to the 3' untranslated region. The interactions between TIA-1 and target transcripts were validated by IP of endogenous mRNAs, followed by reverse transcription and PCR-mediated detection, and by pulldown of biotinylated RNAs, followed by Western blotting. Further studies using RNA interference revealed that TIA-1 repressed the translation of bound mRNAs. In summary, we report a signature motif present in mRNAs that associate with TIA-1 and provide support to the notion that TIA-1 represses the translation of target transcripts.
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页码:9520 / 9531
页数:12
相关论文
共 44 条
[1]  
Anderson P, 2002, CELL STRESS CHAPERON, V7, P213, DOI 10.1379/1466-1268(2002)007<0213:VSTROE>2.0.CO
[2]  
2
[3]  
Anderson P, 2002, J CELL SCI, V115, P3227
[4]   Post-transcriptional regulation of proinflammatory proteins [J].
Anderson, P ;
Phillips, K ;
Stoecklin, G ;
Kedersha, N .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 76 (01) :42-47
[5]   Embryonic lethal abnormal visual RNA-binding proteins involved in growth, differentiation, and posttranscriptional gene expression [J].
Antic, D ;
Keene, JD .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :273-278
[6]   Post-transcriptional regulation of gene expression by degradation of messenger RNAs [J].
Bevilacqua, A ;
Ceriani, MC ;
Capaccioli, S ;
Nicolin, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 195 (03) :356-372
[7]   HuR and mRNA stability [J].
Brennan, CM ;
Steitz, JA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (02) :266-277
[8]   Feedback inhibition of macrophage tumor necrosis factor-α production by tristetraprolin [J].
Carballo, E ;
Lai, WS ;
Blackshear, PJ .
SCIENCE, 1998, 281 (5379) :1001-1005
[9]   Analysis of microarray data using Z score transformation [J].
Cheadle, C ;
Vawter, MP ;
Freed, WJ ;
Becker, KG .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2003, 5 (02) :73-81
[10]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470