An erythromycin resistance cassette and mini-transposon for constructing transcriptional fusions to cat

被引:9
作者
Baron, GS [1 ]
Nano, FE [1 ]
机构
[1] Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8W 3P6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ermC '; F-novicida; mglA; ori(fd); reporter gene; TnMaxErCm;
D O I
10.1016/S0378-1119(99)00032-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A new cassette (Er-Cm cassette) and mini-transposon (mTn) (TnMaxErCm) based on the previously described mTn, TnMax2 [Haas et al., Gene 130, 23-31.], have been constructed. The cassette and mTn make use of an erythromycin resistance (Er-R) marker encoded by ermC'. Both the Er-Cm cassette and TnMaxErCm also carry a promoterless cat gene to allow the construction of transcriptional fusions and the measurement of transcriptional activity by assaying for chloramphenicol acetyltransferase. We show the function of these genetic elements by analyzing the regulation of expression of the mglA gene of Francisella novicida and by using TnMaxErCm to probe for promoter activity within an F. novicida recombinant clone. The reporter cassette and mTn described here further expand the family of TnMax transposons and facilitate the study of gene expression in organisms where direct Tn mutagenesis methods are unavailable. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:59 / 65
页数:7
相关论文
共 25 条
[1]   GROWTH OF FRANCISELLA-SPP IN RODENT MACROPHAGES [J].
ANTHONY, LSD ;
BURKE, RD ;
NANO, FE .
INFECTION AND IMMUNITY, 1991, 59 (09) :3291-3296
[2]   MgIA and MgIB are required for the intramacrophage growth of Francisella novicida [J].
Baron, GS ;
Nano, FE .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :247-259
[3]  
BARON GS, 1998, THESIS U VICTORIA VI
[4]   NUCLEOTIDE-SEQUENCE AND GENOME ORGANIZATION OF FILAMENTOUS BACTERIOPHAGES FL AND FD [J].
BECK, E ;
ZINK, B .
GENE, 1981, 16 (1-3) :35-58
[5]  
BULLOCK WO, 1987, BIOTECHNIQUES, V5, P376
[6]   EVALUATION OF LIVE TULAREMIA VACCINE PREPARED IN A CHEMICALLY DEFINED MEDIUM [J].
CHAMBERL.RE .
APPLIED MICROBIOLOGY, 1965, 13 (02) :232-&
[7]   USE OF XYLE FUSIONS TO DEMONSTRATE THAT LSI-1, A NEISSERIA-GONORRHOEAE LIPOOLIGOSACCHARIDE BIOSYNTHETIC GENE, AND LSI-3 ARE NOT TRANSCRIPTIONALLY LINKED [J].
DANAHER, RJ ;
PETRICOIN, EF ;
STEIN, DC .
JOURNAL OF BACTERIOLOGY, 1994, 176 (11) :3428-3432
[8]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION AND CELL BIOLOGY OF MYCOBACTERIAL INTERACTIONS WITH MACROPHAGES [J].
DHANDAYUTHAPANI, S ;
VIA, LE ;
THOMAS, CA ;
HOROWITZ, PM ;
DERETIC, D ;
DERETIC, V .
MOLECULAR MICROBIOLOGY, 1995, 17 (05) :901-912
[9]   A VERSATILE CLASS OF POSITIVE-SELECTION VECTORS BASED ON THE NONVIABILITY OF PALINDROME-CONTAINING PLASMIDS THAT ALLOWS CLONING INTO LONG POLYLINKERS [J].
ELHAI, J ;
WOLK, CP .
GENE, 1988, 68 (01) :119-138
[10]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051