A novel GFP approach for the analysis of genetic exchange in trypanosomes allowing the in situ detection of mating events

被引:40
作者
Bingle, LEH
Eastlake, JL
Bailey, M
Gibson, WC
机构
[1] Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
[2] Univ Bristol, Dept Vet Clin Sci, Bristol BS40 7DU, Avon, England
来源
MICROBIOLOGY-SGM | 2001年 / 147卷
关键词
Trypanosoma brucei; hybrids; meiosis; Green Fluorescent Protein; tsetse fly;
D O I
10.1099/00221287-147-12-3231
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Trypanosoma brucei undergoes genetic exchange in its insect vector by an unknown mechanism. To visualize the production of hybrids in the fly, a tetracycline (Tet)-inducible expression system was adapted. one parental trypanosome clone was transfected with the gene encoding Green Fluorescent Protein (GFP) under control of the Tet repressor in trans; transfection with these constructs also introduced genes for resistance to hygromycin and phleomycin, respectively. An experimental cross with a second parental clone carrying a gene for geneticin resistance produced fluorescent hybrids with both hygromycin and geneticin resistance. These results are consistent with the meiotic segregation and reassortment of the GFP and repressor genes. Fluorescent hybrids were visible in the salivary glands of the fly, but not the midgut, confirming that genetic exchange occurs among the trypanosome life cycle stages present in (or possibly en route to) the salivary glands. in conclusion, the experimental design has successfully produced fluorescent hybrids which can be observed directly in the salivary glands of the fly, and it has been shown that the recombinant genotypes were most probably the result of meiosis.
引用
收藏
页码:3231 / 3240
页数:10
相关论文
共 39 条
[1]   The PARP promoter of Trypanosoma brucei is developmentally regulated in a chromosomal context [J].
Biebinger, S ;
Rettenmaier, S ;
Flaspohler, J ;
Hartmann, C ;
PenaDiaz, J ;
Wirtz, LE ;
Hotz, HR ;
Barry, JD ;
Clayton, C .
NUCLEIC ACIDS RESEARCH, 1996, 24 (07) :1202-1211
[2]   Vectors for inducible expression of toxic gene products in bloodstream and procyclic Trypanosoma brucei [J].
Biebinger, S ;
Wirtz, LE ;
Lorenz, P ;
Clayton, C .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1997, 85 (01) :99-112
[3]   KINGDOM PROTOZOA AND ITS 18 PHYLA [J].
CAVALIERSMITH, T .
MICROBIOLOGICAL REVIEWS, 1993, 57 (04) :953-994
[4]   NEW CULTURE MEDIUM FOR MAINTENANCE OF TSETSE TISSUES AND GROWTH OF TRYPANOSOMATIDS [J].
CUNNINGHAM, I .
JOURNAL OF PROTOZOOLOGY, 1977, 24 (02) :325-329
[5]   GENETIC EXCHANGE IN TRYPANOSOMA-BRUCEI - EVIDENCE FOR MEIOSIS FROM ANALYSIS OF A CROSS BETWEEN DRUG-RESISTANT TRANSFORMANTS [J].
GIBSON, W ;
BAILEY, M .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 64 (02) :241-252
[6]   GENETIC EXCHANGE IN TRYPANOSOMA-BRUCEI - SELECTION OF HYBRID TRYPANOSOMES BY INTRODUCTION OF GENES CONFERRING DRUG-RESISTANCE [J].
GIBSON, W ;
WHITTINGTON, H .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 60 (01) :19-26
[7]   Intraclonal mating in Trypanosoma brucei is associated with out-crossing [J].
Gibson, W ;
Winters, K ;
Mizen, G ;
Kearns, J ;
Bailey, M .
MICROBIOLOGY-UK, 1997, 143 :909-920
[8]   Kinetoplast DNA minicircles are inherited from both parents in genetic crosses of Trypanosoma brucei [J].
Gibson, W ;
Crow, M ;
Kearns, J .
PARASITOLOGY RESEARCH, 1997, 83 (05) :483-488
[9]   KINETOPLAST DNA MINICIRCLES ARE INHERITED FROM BOTH PARENTS IN GENETIC HYBRIDS OF TRYPANOSOMA-BRUCEI [J].
GIBSON, W ;
GARSIDE, L .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1990, 42 (01) :45-53
[10]   Genetic exchange in the trypanosomatidae [J].
Gibson, W ;
Stevens, J .
ADVANCES IN PARASITOLOGY, VOL 43, 1999, 43 :1-46