Cis-acting elements, CArG-, E-, CCAAT- and TATA-boxes may be involved in sexually regulated gene transcription in Schistosoma mansoni

被引:2
作者
Busek, SU
Fantappie, M
Malaquias, LC
Wilson, RA
Corrêa-Oliveira, R
Oliveira, GC [1 ]
机构
[1] Santa Casa Misericordia Belo Horizonte, Programa Posgrad & Pesquisa, Belo Horizonte, MG, Brazil
[2] Fiocruz MS, Ctr Pesquisas Rene Rachou, BR-30190002 Belo Horizonte, MG, Brazil
[3] Univ Fed Rio de Janeiro, Dept Bioquim, Rio De Janeiro, Brazil
[4] Univ Vale Rio Doce, Lab Imunol, Valadares, MG, Brazil
[5] Univ York, Dept Biol, York YO1 5DD, N Yorkshire, England
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2002年 / 97卷
关键词
Schistosoma mansoni; transcription; promoter; nuclear extract; gel shift analysis;
D O I
10.1590/S0074-02762002000900017
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
Schistosomes undergo various morphological and metabolic changes during their development, reflected in a finely tuned regulation of protein and/or gene expression. The mechanisms involved in the control of gene expression during the development of the parasite are not understood. Two actin genes had been previously cloned and observed to be differentially expressed during the maturation of the parasite. The SmAct gene contains four putative observed to be differentially expressed during the maturation of the parasite. The SmAct gene contains four putative cis-regulatory elements(TATA-,CCAAT-,E- and CArG-boxes). Our objective was to investigate in greater detail the expression pattern of two actin genes and verify if the binding of nuclear proteins to the promoter elements of SmAct correlated with the expression profile observed. We detected little variation in the expression of actin genes during the first seven days of schistosomula culture in vitro. However, we observed significantly higher levels of expression in males compared to female adults. CArG and CCAAT elements bound to a greater extent and formed distinct complexes with mate in comparison to female nuclear extracts. In contrast, female extracts bound weakly to the E-box probe while no binding was observed with male extracts. Taken together these results describe cis-acting elements that appear to be involved in sexually regulated gene expression in Schistosoma mansoni.
引用
收藏
页码:85 / 90
页数:6
相关论文
共 42 条
[1]   ANALYSIS OF ISOFORMS OF ACTIN FROM SCHISTOSOMA-MANSONI BY TWO-DIMENSIONAL GEL-ELECTROPHORESIS [J].
ABBAS, MK ;
CAIN, GD .
PARASITOLOGY RESEARCH, 1989, 76 (02) :178-180
[2]   SCHISTOSOMA-MANSONI - ONE-DIMENSIONAL AND TWO-DIMENSIONAL ELECTROPHORESIS OF PROTEINS SYNTHESIZED INVITRO BY MALES, FEMALES, AND JUVENILES [J].
ATKINSON, BG ;
ATKINSON, KH .
EXPERIMENTAL PARASITOLOGY, 1982, 53 (01) :26-38
[4]   Cardiac tissue enriched factors serum response factor and GATA-4 are mutual coregulators [J].
Belaguli, NS ;
Sepulveda, JL ;
Nigam, V ;
Charron, F ;
Nemer, M ;
Schwartz, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7550-7558
[5]   DELIMITATION AND CHARACTERIZATION OF CIS-ACTING DNA-SEQUENCES REQUIRED FOR THE REGULATED EXPRESSION AND TRANSCRIPTIONAL CONTROL OF THE CHICKEN SKELETAL ALPHA-ACTIN GENE [J].
BERGSMA, DJ ;
GRICHNIK, JM ;
GOSSETT, LMA ;
SCHWARTZ, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (07) :2462-2475
[6]   DEVELOPMENTAL REGULATION OF PROTEIN-SYNTHESIS IN SCHISTOSOMES [J].
BLANTON, RE ;
LICATE, LS .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1992, 51 (02) :201-208
[7]   A 29-NUCLEOTIDE DNA SEGMENT CONTAINING AN EVOLUTIONARILY CONSERVED MOTIF IS REQUIRED IN CIS FOR CELL-TYPE-RESTRICTED REPRESSION OF THE CHICKEN ALPHA-SMOOTH MUSCLE ACTIN GENE CORE PROMOTER [J].
CARROLL, SL ;
BERGSMA, DJ ;
SCHWARTZ, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) :241-250
[8]   Muscle specificity encoded by specific serum response factor-binding sites [J].
Chang, PS ;
Li, L ;
McAnally, J ;
Olson, EN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17206-17212
[9]   Role of basic-helix-loop-helix transcription factors in Sertoli cell differentiation: Identification of an E-box response element in the transferrin promoter [J].
Chaudhary, J ;
Cupp, AS ;
Skinner, MK .
ENDOCRINOLOGY, 1997, 138 (02) :667-675
[10]  
CHOMCZYNSKI P, 1993, BIOTECHNIQUES, V15, P532