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.
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页码:59 / 65
页数:7
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