3′ UTR signals necessary for expression of the Plasmodium gallinaceum ookinete protein, Pgs28, share similarities with those of yeast and plants

被引:10
作者
Cann, H [1 ]
Brown, SV [1 ]
Oguariri, RM [1 ]
Golightly, LM [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Med, Div Int Med & Infect Dis, New York, NY 10021 USA
关键词
3 ' UTR; gene regulation; malaria; sexual stage; protein expression; polyadenylation;
D O I
10.1016/j.molbiopara.2004.06.005
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
During metazoan development, 3' UTR signals mediate the time and place of gene expression. For protozoan Plasmodium parasites, the formation of ookinetes from gametes in the mosquito midgut is an analogous developmental process. Previous studies of the 3' UTR signals necessary for expression of Pgs28, the major surface protein of Plasmodium gallinaceum ookinetes, suggested that a 3' UTR T-rich region and DNA sequences containing an ATTAAA eukaryotic polyadenylation consensus motif were necessary for its expression. During metazoan development, U-rich elements may function in conjunction with eukaryotic polyadenylation consensus signals to mediate developmental protein expression. To define whether the putative Plasmodium elements were mediators of Pgs28 expression mutations of these nucleotide sequences were made in plasmid constructs. The effect of the mutations on Pgs28 expression was tested by the transient gene transfection of sexual stage P. gallinaceum parasites. These studies reveal that two different mutations of the ATTAAA motif, which alter gene expression in higher eukaryotes and yeast, do not alter the expression of Pgs28. However, the U-rich element, adjacent nucleotides UUUACAAAAUUGUUUUAACU and downstream nucleotides UAUAUAAAA are able to mediate expression to varying degrees. The organization and overlapping function of these elements appears to more closely resemble that of yeasts or plants than those of metazoans. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 245
页数:7
相关论文
共 44 条
[1]   Translational control of cyclin B1 mRNA during meiotic maturation: Coordinated repression and cytoplasmic polyadenylation [J].
Barkoff, AF ;
Dickson, KS ;
Gray, NK ;
Wickens, N .
DEVELOPMENTAL BIOLOGY, 2000, 220 (01) :97-109
[2]   The transcriptome of the intraerythrocytic developmental cycle of Plasmodium falciparum [J].
Bozdech, Z ;
Llinás, M ;
Pulliam, BL ;
Wong, ED ;
Zhu, JC ;
DeRisi, JL .
PLOS BIOLOGY, 2003, 1 (01) :85-100
[3]   The malaria parasite Plasmodium falciparum encodes members of the Puf RNA-binding protein family with conserved RNA binding activity [J].
Cui, LW ;
Fan, Q ;
Li, JF .
NUCLEIC ACIDS RESEARCH, 2002, 30 (21) :4607-4617
[4]   TRANSLATIONAL REGULATION IN DEVELOPMENT [J].
CURTIS, D ;
LEHMANN, R ;
ZAMORE, PD .
CELL, 1995, 81 (02) :171-178
[5]   Post-transcriptional gene regulatory mechanisms in eukaryotes: an overview [J].
Day, DA ;
Tuite, MF .
JOURNAL OF ENDOCRINOLOGY, 1998, 157 (03) :361-371
[6]   DIVERSITY OF CYTOPLASMIC FUNCTIONS FOR THE 3' UNTRANSLATED REGION OF EUKARYOTIC TRANSCRIPTS [J].
DECKER, CJ ;
PARKER, P .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (03) :386-392
[7]   Recognition of polyadenylation sites in yeast pre-mRNAs by cleavage and polyadenylation factor [J].
Dichtl, B ;
Keller, W .
EMBO JOURNAL, 2001, 20 (12) :3197-3209
[8]   A novel malaria protein, Pfs28, and Pfs25 are genetically linked and synergistic as falciparum malaria transmission-blocking vaccines [J].
Duffy, PE ;
Kaslow, DC .
INFECTION AND IMMUNITY, 1997, 65 (03) :1109-1113
[9]   PGS28 BELONGS TO A FAMILY OF EPIDERMAL GROWTH-FACTOR LIKE ANTIGENS THAT ARE TARGETS OF MALARIA TRANSMISSION-BLOCKING ANTIBODIES [J].
DUFFY, PE ;
PIMENTA, P ;
KASLOW, DC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :505-510
[10]   THE SEQUENCE 5'-AAUAAA-3' FORMS PART OF THE RECOGNITION SITE FOR POLYADENYLATION OF LATE SV40 MESSENGER-RNAS [J].
FITZGERALD, M ;
SHENK, T .
CELL, 1981, 24 (01) :251-260