The Drosophila hnRNPA/B homolog, Hrp48, is specifically required for a distinct step in osk mRNA localization

被引:87
作者
Huynh, JR
Munro, TP
Smith-Litière, K
Lepesant, JA
Johnston, DS
机构
[1] Univ Cambridge, Wellcome Trust Canc Res UK, Gurdon Inst, Cambridge CB2 1QR, England
[2] Univ Cambridge, Dept Genet, Cambridge CB2 1QR, England
[3] Univ Paris 06, Inst Jacques Monod, CNRS, F-75251 Paris 05, France
[4] Univ Paris 07, Inst Jacques Monod, CNRS, F-75251 Paris 05, France
基金
英国惠康基金;
关键词
D O I
10.1016/S1534-5807(04)00130-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Staufen-dependent localization of oskar mRNA to the posterior of the Drosophila oocyte induces the formation of the pole plasm, which contains the abdominal and germline determinants. In a germline clone screen for mutations that disrupt the posterior localization of GFP-Staufen, we isolated three missense alleles in the hnRNPA/B homolog, Hrp48. These mutants specifically abolish osk mRNA localization, without affecting its translational control or splicing, or the localization of bicoid and gurken mRNAs and the organization of the microtubule cytoskeleton. Hrp48 colocalizes with osk mRNA throughout oogenesis, and interacts with its 5' and 3' regulatory regions, suggesting that it binds directly to oskar mRNA to mediate its posterior transport. The hrp48 alleles cause a different oskar mRNA localization defect from other mutants, and disrupt the formation of GFP-Staufen particles. This suggests a new step in the localization pathway, which may correspond to the assembly of Staufen/oskar mRNA transport particles.
引用
收藏
页码:625 / 635
页数:11
相关论文
共 81 条
[1]   TRANSPORT AND LOCALIZATION OF EXOGENOUS MYELIN BASIC-PROTEIN MESSENGER-RNA MICROINJECTED INTO OLIGODENDROCYTES [J].
AINGER, K ;
AVOSSA, D ;
MORGAN, F ;
HILL, SJ ;
BARRY, C ;
BARBARESE, E ;
CARSON, JH .
JOURNAL OF CELL BIOLOGY, 1993, 123 (02) :431-441
[2]   Localization and anchoring of mRNA in budding yeast [J].
Beach, DL ;
Salmon, ED ;
Bloom, K .
CURRENT BIOLOGY, 1999, 9 (11) :569-578
[3]   Localization of ASH1 mRNA particles in living yeast [J].
Bertrand, E ;
Chartrand, P ;
Schaefer, M ;
Shenoy, SM ;
Singer, RH ;
Long, RM .
MOLECULAR CELL, 1998, 2 (04) :437-445
[4]   ANALYSIS OF THE RNA-RECOGNITION MOTIF AND RS AND RGG DOMAINS - CONSERVATION IN METAZOAN PRE-MESSENGER-RNA SPLICING FACTORS [J].
BIRNEY, E ;
KUMAR, S ;
KRAINER, AR .
NUCLEIC ACIDS RESEARCH, 1993, 21 (25) :5803-5816
[5]   A function for kinesin I in the posterior transport of oskar mRNA and Staufen protein [J].
Brendza, RP ;
Serbus, LR ;
Duffy, JB ;
Saxton, WM .
SCIENCE, 2000, 289 (5487) :2120-2122
[6]   Intracellular trafficking of HnRNP A2 in oligodendrocytes [J].
Brumwell, C ;
Antolik, C ;
Carson, JH ;
Barbarese, E .
EXPERIMENTAL CELL RESEARCH, 2002, 279 (02) :310-320
[7]  
Burnette JM, 1999, GENETICS, V151, P1517
[8]  
Carson JH, 1997, CELL MOTIL CYTOSKEL, V38, P318, DOI 10.1002/(SICI)1097-0169(1997)38:4<318::AID-CM2>3.0.CO
[9]  
2-#
[10]   hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins [J].
Cartegni, L ;
Maconi, M ;
Morandi, E ;
Cobianchi, F ;
Riva, S ;
Biamonti, G .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 259 (03) :337-348