TcRho1 of Trypanosoma cruzi:: role in metacyclogenesis and cellular localization

被引:13
作者
de Melo, LDB
Nepomuceno-Silva, JL
Sant'Anna, C
Eisele, N
Ferraro, RB
Meyer-Fernandes, JR
de Souza, W
Cunha-e-Silva, NL
Lopes, UG [1 ]
机构
[1] Univ Fed Rio de Janeiro, CCS, Inst Biofis Carlos Chagas Filho, Mol Parasitol Lab, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, CCS, Inst Biofis Carlos Chagas Filho, Lab Ultraestrutura Celular Hertha Meyer, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, CCS, Dept Bioquim Med, Lab Bioquim Celular, Rio De Janeiro, Brazil
关键词
Trypanosoma cruzi; GTPase; Rho; TcRho1;
D O I
10.1016/j.bbrc.2004.08.197
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
Here we have investigated the function of TcRho1, a Rho family orthologue from the parasite Trypanosoma cruzi. We have selected parasites overexpressing wild-type TeRho1 and a truncated form of TeRho1 (TcRho1-DeltaCaaX) which is unable to undergo farnesylation and supposed to interfere with recruitment of Rho effectors to membranes. TcRho1 protein was localized at the anterior region of wild-type and TcRho1 overexpressing epimastigotes, suggesting association with the Golgi apparatus. Accordingly, parasites overexpressing TcRho1-DeltaCaaX presented cytoplasmic fluorescence. To address the function of TcRho1 during differentiation, from epimastigotes to trypomastigotes, we submitted parasites overexpressing the above-cited lineages to metacyclogenesis assays. Parasites overexpressing TcRho1-ACaaX generated a discrete number of metacyclic trypomastigotes when Compared with other lineages. strikingly, TcRho1-DeltaCaaX cells died synchronously during the process of metacyclogenesis. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1009 / 1016
页数:8
相关论文
共 38 条
[11]   GTPases in protozoan parasites: Tools for cell biology and chemotherapy [J].
Field, MC ;
Ali, BRS ;
Field, H .
PARASITOLOGY TODAY, 1999, 15 (09) :365-371
[12]  
Figueiredo RCBQ, 2000, J PARASITOL, V86, P1213, DOI 10.1645/0022-3395(2000)086[1213:DOTCEM]2.0.CO
[13]  
2
[14]   Protein farnesyl and N-myristoyl transferases:: piggy-back medicinal chemistry targets for the development of antitrypanosomatid and antimalarial therapeutics [J].
Gelb, MH ;
Van Voorhis, WC ;
Buckner, FS ;
Yokoyama, K ;
Eastman, R ;
Carpenter, EP ;
Panethymitaki, C ;
Brown, KA ;
Smith, DF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2003, 126 (02) :155-163
[15]   USING SIMULTANEOUS, TANDEM GENE REPLACEMENTS TO STUDY EXPRESSION OF THE MULTICOPY UBIQUITIN-FUSION (FUS) GENE FAMILY OF TRYPANOSOMA-CRUZI [J].
GILLESPIE, RD ;
AJIOKA, J ;
SWINDLE, J .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 60 (02) :281-292
[16]   Trypanosoma cruzi:: Cloning and characterization of a RAB7 gene [J].
Leal, ST ;
Araripe, JR ;
Ürményi, TP ;
Cross, GAM ;
Rondinelli, E .
EXPERIMENTAL PARASITOLOGY, 2000, 96 (01) :23-31
[17]   Heterogeneity of Entamoeba histolytica rac genes encoding p21(rac) homologues [J].
Lohia, A ;
Samuelson, J .
GENE, 1996, 173 (02) :205-208
[18]   THE SMALL GTP-BINDING PROTEIN RHO1P IS LOCALIZED ON THE GOLGI-APPARATUS AND POST-GOLGI VESICLES IN SACCHAROMYCES-CEREVISIAE [J].
MCCAFFREY, M ;
JOHNSON, JS ;
GOUD, B ;
MYERS, AM ;
ROSSIER, J ;
POPOFF, MR ;
MADAULE, P ;
BOQUET, P .
JOURNAL OF CELL BIOLOGY, 1991, 115 (02) :309-319
[19]   Characterization of the association of the actin-binding protein, IQGAP, and activated Cdc42 with Golgi membranes [J].
McCallum, SJ ;
Erickson, JW ;
Cerione, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22537-22544
[20]  
Mendonca Sergio M., 1993, Biological Research, V26, P3