UNIVERSAL BARRIER TO LATERAL SPREAD OF SPECIFIC GENES AMONG MICROORGANISMS

被引:57
作者
DIAZ, E [1 ]
MUNTHALI, M [1 ]
DELORENZO, V [1 ]
TIMMIS, KN [1 ]
机构
[1] CSIC, CTR INVEST BIOL, E-28006 MADRID, SPAIN
关键词
D O I
10.1111/j.1365-2958.1994.tb00477.x
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
A genetic circuit to suppress the lateral spread of cloned genes from recombinant to indigenous microorganisms in the environment has been developed. It is based on the endonucleolytic activity of the bacterial toxin colicin E3, which has a distinct target at the 3' end of the 16S ribosomal RNA; this sequence is conserved in virtually all prokaryotic and many eukaryotic genera. Cleavage at this sequence separates the mRNA binding sites from the remainder of the 16S rRNA, thereby inhibiting protein synthesis. While host bacteria carrying the genes for both colicin production and colicin immunity are perfectly viable, lateral transfer of the E3 gene to non-immune recipients results in killing of such recipients. This genetic circuit decreases operational transfer frequencies of cloned genes linked to the E3 gene among a variety of bacterial genera by four to five orders of magnitude. In combination with transposon cloning vectors, the circuit is predicted to reduce the rate of lateral spread of specific genes to ecologically insignificant levels. This system therefore represents a useful tool both to explore the evolutionary and ecological consequences of experimentally reducing lateral gene spread among microorganisms, and to increase the ecological predictability of novel recombinant microorganisms.
引用
收藏
页码:855 / 861
页数:7
相关论文
共 34 条
[1]  
BERG CM, 1989, MOBILE DNA, P879
[2]   BIOLOGY OF DNA RESTRICTION [J].
BICKLE, TA ;
KRUGER, DH .
MICROBIOLOGICAL REVIEWS, 1993, 57 (02) :434-450
[3]  
BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
[4]   A COMPLEMENTATION ANALYSIS OF RESTRICTION AND MODIFICATION OF DNA IN ESCHERICHIA COLI [J].
BOYER, HW ;
ROULLAND.D .
JOURNAL OF MOLECULAR BIOLOGY, 1969, 41 (03) :459-&
[5]  
BRAZIL D, 1993, 4TH INT S PSEUD BIOT, P50
[6]   ANALYSIS OF THE PROMOTERS FOR THE 2 IMMUNITY GENES PRESENT IN THE COLE3-CA38 PLASMID USING 2 NEW PROMOTER PROBE VECTORS [J].
CHAK, KF ;
JAMES, R .
NUCLEIC ACIDS RESEARCH, 1985, 13 (07) :2519-2531
[7]   COMPILATION OF SMALL RIBOSOMAL-SUBUNIT RNA SEQUENCES [J].
DAMS, E ;
HENDRIKS, L ;
VANDEPEER, Y ;
NEEFS, JM ;
SMITS, G ;
VANDENBEMPT, I ;
DEWACHTER, R .
NUCLEIC ACIDS RESEARCH, 1988, 16 :R87-R173
[8]   ANALYSIS OF PSEUDOMONAS GENE-PRODUCTS USING LACIQ PTRP-LAC PLASMIDS AND TRANSPOSONS THAT CONFER CONDITIONAL PHENOTYPES [J].
DELORENZO, V ;
ELTIS, L ;
KESSLER, B ;
TIMMIS, KN .
GENE, 1993, 123 (01) :17-24
[9]  
DELORENZO V, 1994, METHOD ENZYMOL, V235, P386
[10]   PROPERTIES OF 6 PESTICIDE DEGRADATION PLASMIDS ISOLATED FROM ALCALIGENES-PARADOXUS AND ALCALIGENES-EUTROPHUS [J].
DON, RH ;
PEMBERTON, JM .
JOURNAL OF BACTERIOLOGY, 1981, 145 (02) :681-686