Protein expression is increased by a class III AU-rich element and tethered CUG-BP1

被引:25
作者
Barreau, Carine [1 ]
Watrin, Tanguy [1 ]
Osborne, H. Beverley [1 ]
Paillard, Luc [1 ]
机构
[1] Univ Rennes 1, CNRS, UMR 6061, IFRI40, F-35043 Rennes, France
关键词
AU-rich element (ARE); post-transcriptional control; embryo deadenylation element-binding protein (EDEN-BP); c-jun; RNA-binding proteins; Xenopus laevis; translation;
D O I
10.1016/j.bbrc.2006.06.177
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
In mammalian somatic cells, the post-transcriptional control of cytokine or proto-oneogene expression is often achieved by factors binding to sequence elements in the 3' untranslated region (3'UTR). The most studied are the AU-rich elements (ARE) that have been divided into three classes. Here, we show that in mammalian cells, the presence of the class III c-jun ARE in the 3'UTR of a reporter mRNA enhanced reporter protein expression. In contrast, the presence of a class II ARE in the 3'UTR decreased reporter protein expression. CUG-BP1/CELF1 is able to bind c-jun ARE. Protein expression was enhanced similarly to what was observed for c-jun ARE when the reporter mRNA contained a synthetic CUG-BP1/CELF1-binding site, or when this protein was tethered to the 3'UTR of a reporter mRNA. These results reveal an unexpected complexity of ARE-mediated post-transcriptional regulations, and indicate a function for CUG-BP1/CELF1 in class III ARE directed regulations., (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:723 / 730
页数:8
相关论文
共 32 条
[21]   Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1 [J].
Lykke-Andersen, J ;
Wagner, E .
GENES & DEVELOPMENT, 2005, 19 (03) :351-361
[22]   POLY(A) ELONGATION DURING XENOPUS OOCYTE MATURATION IS REQUIRED FOR TRANSLATIONAL RECRUITMENT AND IS MEDIATED BY A SHORT SEQUENCE ELEMENT [J].
MCGREW, LL ;
DWORKINRASTL, E ;
DWORKIN, MB ;
RICHTER, JD .
GENES & DEVELOPMENT, 1989, 3 (06) :803-815
[23]   Coupled mRNA stabilization and translational silencing of cyclooxygenase-2 by a novel RNA binding protein, CUGBP2 [J].
Mukhopadhyay, D ;
Houchen, CW ;
Kennedy, S ;
Dieckgraefe, BK ;
Anant, S .
MOLECULAR CELL, 2003, 11 (01) :113-126
[24]   A network of immediate early gene products propagates subtle differences in mitogen-activated protein kinase signal amplitude and duration [J].
Murphy, LO ;
MacKeigan, JP ;
Blenis, J .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (01) :144-153
[25]   Control of mRNA translation and stability in haematopoietic cells: The function of hnRNPs K and E1/E2 [J].
Ostareck-Lederer, A ;
Ostareck, DH .
BIOLOGY OF THE CELL, 2004, 96 (06) :407-411
[26]   c-Jun ARE targets mRNA deadenylation by an EDEN-BP (embryo deadenylation element-binding protein)-dependent pathway [J].
Paillard, L ;
Legagneux, V ;
Maniey, D ;
Osborne, HB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3232-3235
[27]   East of EDEN was a poly(A) tail [J].
Paillard, L ;
Osborne, HB .
BIOLOGY OF THE CELL, 2003, 95 (3-4) :211-219
[28]  
Peng SSY, 1996, MOL CELL BIOL, V16, P1490
[29]   Roles of AUF1 isoforms, HuR and BRF1 in ARE-dependent mRNA turnover studied by RNA interference [J].
Raineri, I ;
Wegmueller, D ;
Gross, B ;
Certa, U ;
Moroni, C .
NUCLEIC ACIDS RESEARCH, 2004, 32 (04) :1279-1288
[30]   The CUG-binding protein binds specifically to UG dinucleotide repeats in a yeast three-hybrid system [J].
Takahashi, N ;
Sasagawa, N ;
Suzuki, K ;
Ishiura, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 277 (02) :518-523