Dimerization of the 3′UTR of bicoid mRNA involves a two-step mechanism

被引:41
作者
Wagner, C
Palacios, I
Jaeger, L
St Johnston, D
Ehresmann, B
Ehresmann, C
Brunel, C
机构
[1] Inst Biol Mol & Cellulaire, CNRS, UPR 9002, F-67084 Strasbourg, France
[2] Wellcome CRC Inst, Cambridge CB2 1QR, England
关键词
RNA dimerization; RNA localization; RNA-protein interactions; bcd mRNA; Staufen;
D O I
10.1006/jmbi.2001.5057
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 proper localization of bicoid (bcd) mRNA requires cis-acting signals within its 3' untranslated region (UTR) and trans-acting factors such as Staufen. Dimerization of bcd mRNA through intermolecular base-pairing between two complementary loops of domain III of the 3'UTR was pro posed to be important for particle formation in the embryo. The participation m the dimerization process of each domain building the 3'UTR Cambridge Tennis Tennis Court Court Road was evaluated by thermodynamic and kinetic analysis of various, mutated and truncated RNAs. Although sequence complementarity between the two loops of domain III is required for initiating mRNA dimerization, the initial reversible loop-loop complex is converted rapidly into an almost irreversible complex. This conversion involves parts of RNA outside of domain III that promote initial recognition, and dimerization can be inhibited by sense or antisense oligonucleotides only before conversion has proceeded. Injection of the different bcd RNA variants into living Drosophila embryos shows that all elements that inhibit RNA dimerization in vitro prevent formation of localized particles containing Staufen. Particle formation appeared to be dependent on both mRNA dimerization and other element(s) in domains IV and V. Domain III of bcd mRNA could be substituted by heterologous dimerization motifs of different geometry. The resulting dimers were converted into stable forms, independently of the dimerization module used. Moreover, these chimeric RNAs were competent in forming localized particles and recruiting Staufen. The finding that the dimerization domain of bcd mRNA is interchangeable suggests that dimerization by itself, and not the precise geometry of the intermolecular interactions, is essential for the localization process. This suggests that the stabilizing interactions that are formed during the second step of the dimerization process might represent crucial elements for Staufen recognition and localization. (C) 2001 Academic Press.
引用
收藏
页码:511 / 524
页数:14
相关论文
共 50 条
[1]   Structural basis for binding of the plasmid ColIb-P9 antisense Inc RNA to its target RNA with the 5′-rUUGGCG-3′ motif in the loop sequence [J].
Asano, K ;
Niimi, T ;
Yokoyama, S ;
Mizobuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11826-11838
[2]   Structural analysis of late intermediate complex formed between plasmid ColIb-P9 Inc RNA and its target RNA - How does a single antisense RNA repress translation of two genes at different rates? [J].
Asano, K ;
Mizobuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (02) :1269-1274
[3]   RNA localization in development [J].
Bashirullah, A ;
Cooperstock, RL ;
Lipshitz, HD .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :335-394
[4]   Role of the DIS hairpin in replication of human immunodeficiency virus type 1 [J].
Berkhout, B ;
vanWamel, JLB .
JOURNAL OF VIROLOGY, 1996, 70 (10) :6723-6732
[5]   GFP IN DROSOPHILA [J].
BRAND, A .
TRENDS IN GENETICS, 1995, 11 (08) :324-325
[6]   A dimer as a building block in assembling RNA - A hexamer that gears bacterial virus phi29 DNA-translocating machinery [J].
Chen, CP ;
Sheng, ST ;
Shao, ZF ;
Guo, PX .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17510-17516
[7]   Requirements for kissing-loop-mediated dimerization of human immunodeficiency virus RNA [J].
Clever, JL ;
Wong, ML ;
Parslow, TG .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5902-5908
[8]   Rules for RNA recognition of GNRA tetraloops deduced by in vitro selection: Comparison with in vivo evolution [J].
Costa, M ;
Michel, F .
EMBO JOURNAL, 1997, 16 (11) :3289-3302
[9]   Solution studies of the dimerization initiation site of HIV-1 genomic RNA [J].
Dardel, F ;
Marquet, R ;
Ehresmann, C ;
Ehresmann, B ;
Blanquet, S .
NUCLEIC ACIDS RESEARCH, 1998, 26 (15) :3567-3571
[10]   FIRST GLIMPSES AT STRUCTURE-FUNCTION-RELATIONSHIPS OF THE NUCLEOCAPSID PROTEIN OF RETROVIRUSES [J].
DARLIX, JL ;
LAPADATTAPOLSKY, M ;
DEROCQUIGNY, H ;
ROQUES, BP .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 254 (04) :523-537