Regulatory sequences and a novel gene in the msp (GP63) gene cluster of Leishmania chagasi

被引:22
作者
McCoy, JJ
Beetham, JK
Ochs, DE
Donelson, JE
Wilson, ME [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
[4] VA Med Ctr, Iowa City, IA 52242 USA
关键词
Leishmania; gene organization; gene expression; GP63;
D O I
10.1016/S0166-6851(98)00112-1
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 surface protease GP63 of Leishmania chagasi is encoded by a cluster of more than 18 tandem major surface protease (msp) genes belonging to three classes (mspL, mspS, mspC). mspL and mspS transcripts are differentially expressed during parasite growth. RNAs from mspS genes predominate during stationary phase, the time when parasite virulence and GP63 expression are maximal. We hypothesized that the unique regions downstream of mspS genes contain signals important for gene expression. The 2.8 kb region between tandem mspS genes was found to contain an 882 bp open reading frame designated mag. Copies of mag were found downstream of all mspS genes in the cluster, mag hybridized faintly to bands on Northern blots and a fully processed mag cDNA was identified in a promastigote cDNA library, providing evidence that mag genes are expressed at low levels. Similar to mspS RNAs, the abundance of mag RNAs was greater in stationary phase than logarithmic phase organisms, although mag RNAs were less abundant than mspS RNAs throughout growth. Northern blots and enzyme assays of promastigotes containing plasmid constructs in which the beta-galactosidase gene was followed by sequences between mspS coding regions, either with or without mag and its downstream sequences, suggest these regions have several regulatory effects accounting for the growth-associated changes in mspS expression. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:251 / 265
页数:15
相关论文
共 37 条
[1]   Glycoprotein 46 mRNA abundance is post-transcriptionally regulated during development of Leishmania chagasi promastigotes to an infectious form [J].
Beetham, JK ;
Myung, KS ;
McCoy, JJ ;
Wilson, ME ;
Donelson, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (28) :17360-17366
[2]  
Berberof M, 1996, MOL CELL BIOL, V16, P914
[3]   SIMPLE MONOPHASIC MEDIUM FOR AXENIC CULTURE OF HEMOFLAGELLATES [J].
BERENS, RL ;
BRUN, R ;
KRASSNER, SM .
JOURNAL OF PARASITOLOGY, 1976, 62 (03) :360-365
[4]   THE PROMASTIGOTE SURFACE PROTEASE OF LEISHMANIA [J].
BORDIER, C .
PARASITOLOGY TODAY, 1987, 3 (05) :151-153
[5]  
CHANG KP, 1990, ANNU REV MICROBIOL, V44, P499, DOI 10.1146/annurev.mi.44.100190.002435
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   STABLE DNA TRANSFECTION OF A WIDE-RANGE OF TRYPANOSOMATIDS [J].
COBURN, CM ;
OTTEMAN, KM ;
MCNEELY, T ;
TURCO, SJ ;
BEVERLEY, SM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1991, 46 (01) :169-180
[8]   COORDINATE TRANSCRIPTION OF VARIANT SURFACE GLYCOPROTEIN GENES AND AN EXPRESSION SITE ASSOCIATED GENE FAMILY IN TRYPANOSOMA BRUCEI [J].
CULLY, DF ;
IP, HS ;
CROSS, GAM .
CELL, 1985, 42 (01) :173-182
[9]   METACYCLOGENESIS IS A MAJOR DETERMINANT OF LEISHMANIA PROMASTIGOTE VIRULENCE AND ATTENUATION [J].
DASILVA, R ;
SACKS, DL .
INFECTION AND IMMUNITY, 1987, 55 (11) :2802-2806
[10]   GENE-EXPRESSION IN LEISHMANIA - ANALYSIS OF ESSENTIAL 5' DNA-SEQUENCES [J].
DELAFAILLE, MAC ;
LABAN, A ;
WIRTH, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2703-2707