Leishmania mexicana:: Identification of genes that are preferentially expressed in amastigotes

被引:26
作者
Bellatin, JA
Murray, AS
Zhao, M
McMaster, WR
机构
[1] Univ British Columbia, Dept Med Genet, Vancouver, BC V6H 3Z6, Canada
[2] Vancouver Hosp Jack Bell Res Ctr, Immunol Res Ctr, Vancouver, BC V6H 3Z6, Canada
基金
加拿大健康研究院;
关键词
Leishmania mexicana; amastigote; gene expression;
D O I
10.1006/expr.2001.4677
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The protozoan parasite Leishmania has a digenetic life cycle, alternating between the promastigote and the amastigote stages. Amastigotes infect macrophage cells and reside in the hydrolytic environment of the phagolysosome. Leishmania show distinct morphological and biochemical changes during differentiation into amastigotes. These alterations are believed to be regulated by stage-specific expression of a discrete number of genes. Selective-suppression PCR, a PCR-based subtractive hybridization technique, identified two genes preferentially expressed in L. mexicana lesion amastigotes: a novel gene family, A600, and a differentially expressed beta-tubulin gene. Northern blot analysis confirmed amastigote-specific expression of these genes and quantitation showed a sixfold higher abundance of A600 and beta-tubulin transcripts in lesion amastigotes. The A600 gene was predicted to contain a 293-bp open reading frame (ORF) that was tandemly repeated in the L. mexicana genome. Sequence analysis predicted that the A600 ORF encodes either a membrane-bound or a secreted protein that may have a functional role in amastigote differentiation or intraphagolysosomal parasite survival. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:44 / 53
页数:10
相关论文
共 36 条
[1]   RECURRENT CUTANEOUS LEISHMANIASIS - A ROLE FOR PERSISTENT PARASITES [J].
AEBISCHER, T .
PARASITOLOGY TODAY, 1994, 10 (01) :25-28
[2]   TRANSSPLICING OF NUCLEAR PRE-MESSENGER-RNAS [J].
AGABIAN, N .
CELL, 1990, 61 (07) :1157-1160
[3]  
ALEXANDER J, 1992, ADV PARASIT, V31, P75
[4]  
BOGDAN C, 1998, INT J PARASITOL, V28, P2
[5]   Differential regulation of multiple glucose transporter genes in Leishmania mexicana [J].
Burchmore, RJS ;
Landfear, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :29118-29126
[6]   MOLECULAR-CLONING OF THE MAJOR SURFACE-ANTIGEN OF LEISHMANIA [J].
BUTTON, LL ;
MCMASTER, WR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (02) :724-729
[7]   The developmental expression of Leishmania donovani A2 amastigote-specific genes is post-transcriptionally mediated and involves elements located in the 3'-untranslated region [J].
Charest, H ;
Zhang, WW ;
Matlashewski, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) :17081-17090
[8]   DEVELOPMENTAL GENE-EXPRESSION IN LEISHMANIA-DONOVANI - DIFFERENTIAL CLONING AND ANALYSIS OF AN AMASTIGOTE-STAGE-SPECIFIC GENE [J].
CHAREST, H ;
MATLASHEWSKI, G .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :2975-2984
[9]   Differential expression of Leishmania major beta-tubulin genes during the acquisition of promastigote infectivity [J].
Coulson, RMR ;
Conner, V ;
Chen, JC ;
Ajioka, JW .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1996, 82 (02) :227-236
[10]   Prediction of transmembrane alpha-helices in prokaryotic membrane proteins: the dense alignment surface method [J].
Cserzo, M ;
Wallin, E ;
Simon, I ;
vonHeijne, G ;
Elofsson, A .
PROTEIN ENGINEERING, 1997, 10 (06) :673-676