Bacterial DNA methylation and gene transfer efficiency

被引:14
作者
Allamane, S [1 ]
Jourdes, P [1 ]
Ratel, D [1 ]
Vicat, JM [1 ]
Dupré, I [1 ]
Lainé, M [1 ]
Berger, F [1 ]
Benabid, AL [1 ]
Wion, D [1 ]
机构
[1] CHU Michallon, INSERM U318, F-38043 Grenoble 09, France
关键词
plasmid; bacteria; Dam; Dcm; gene therapy; patent;
D O I
10.1006/bbrc.2000.3603
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
The necessary amplification step in bacteria of any plasmid currently used in DNA immunization or gene therapy introduces modification in the nucleotide sequence of plasmid DNA used in gene transfer. These changes affect the adenine and the internal cytosine in respectively all of the GATC and CC(A/T)GG sequences. These modifications which introduce 6-methyladenine and 5-methylcytosine in plasmidic DNA are the consequence of the existence of the bacterial modification systems Dam and Dcm. In eucaryotes, the presence of B-methylcytosine at dinucleotides -CG- is involved in silencing gene expression, bud the possible consequences of the presence of the bacterial G(m)ATC and (CC)-C-m(A/T)GG sequences in the plasmids used in gene transfer experiments are presently unknown. Since the possibility exists to obtain plasmid DNA lacking this specific bacterial pattern of methylation by using (dam(-), dcm(-)) bacteria we performed experiments to compare in vitro and in vivo gene transfer efficiency of a pCMV-luc reporter plasmid amplified either in the JM109 (dam(+), dcm(+)) or JM110 (dam(-), dcm(-)) bacteria. Data obtained demonstrated that the presence of 6-methyladenine in GATC sequences and 5-methylcytosine in the second C of CC(A/T)GG motifs does not reduce the levels of luciferase activity detected following in vitro or in vivo gene transfer. On the contrary, gene transfer with a pCMV-luc amplified in JM109 (dam(+), dcm(+)) bacteria gives greater amounts of luciferase than the same transfection performed with a plasmid amplified in the mutated JM110 (dam(-), dcm(-)) counterpart. Therefore, these data do not suggest that the use of (dam(-), dcm(-)) bacteria to amplify plasmid DNA may increase gene transfer efficiency. However, the persistence of the use of (dam(+) dcm(+)) bacteria in order to amplify plasmid DNA raises the question of the possible biological consequences of the introduction of the bacterial G(m)ATC and (CC)-C-m(A/T)GG sequences in eukaryotic cells or organisms. (C) 2000 Academic Press.
引用
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页码:1261 / 1264
页数:4
相关论文
共 16 条
[1]   THE GREAT GATC - DNA METHYLATION IN ESCHERICHIA-COLI [J].
BARRAS, F ;
MARINUS, MG .
TRENDS IN GENETICS, 1989, 5 (05) :139-143
[2]   Are sequences of plasmid DNA used in gene therapy erroneous? [J].
Berger, F ;
Canova, C ;
Benabid, AL ;
Wion, D .
NATURE BIOTECHNOLOGY, 1999, 17 (06) :517-517
[3]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[4]   DNA METHYLATION AND CELLULAR AGING [J].
CATANIA, J ;
FAIRWEATHER, DS .
MUTATION RESEARCH, 1991, 256 (2-6) :283-293
[5]   MOLECULAR-BASIS OF BASE SUBSTITUTION HOTSPOTS IN ESCHERICHIA-COLI [J].
COULONDRE, C ;
MILLER, JH ;
FARABAUGH, PJ ;
GILBERT, W .
NATURE, 1978, 274 (5673) :775-780
[6]   How are alkynes scrambled? [J].
Bunz, UHF .
SCIENCE, 2005, 308 (5719) :216-217
[7]   CpG motifs present in bacterial DNA rapidly induce lymphocytes to secrete interleukin 6, interleukin 12, and interferon gamma [J].
Klinman, DM ;
Yi, AK ;
Beaucage, SL ;
Conover, J ;
Krieg, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :2879-2883
[8]   THE DAM AND DCM STRAINS OF ESCHERICHIA-COLI - A REVIEW [J].
PALMER, BR ;
MARINUS, MG .
GENE, 1994, 143 (01) :1-12
[9]  
RATEL D, 2000, J NATL CANC I
[10]   CpG methylation, chromatin structure and gene silencing - a three-way connection [J].
Razin, A .
EMBO JOURNAL, 1998, 17 (17) :4905-4908