A new approach using multiplex long accurate PCR and yeast artificial chromosomes for bacterial chromosome mapping and sequencing

被引:32
作者
Sorokin, A
Lapidus, A
Capuano, V
Galleron, N
Pujic, P
Ehrlich, SD
机构
[1] Lab. de Genet. Microbienne, Inst. Natl. de la Rech. Agronomique, Domaine de Vilvert
来源
GENOME RESEARCH | 1996年 / 6卷 / 05期
关键词
D O I
10.1101/gr.6.5.448
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
An efficient approach for structural studies on bacterial chromosomes is presented. It is based on high-resolution PCR map construction by using a multiplex long accurate PCR (MLA PCR) protocol and a YAC clone carrying the region to be mapped as indicator. The high-resolution PCR map of the Bacillus subtilis rmB-dnaB region is presented as an example. Data are also presented on the use of DNA generated by LA PCR for sequencing; they are relevant to LA PCR induced mutations and justify the application of such mapping for sequencing long stretches of bacterial chromosomes.
引用
收藏
页码:448 / 453
页数:6
相关论文
共 17 条
[1]  
Anagnostopoulos C., 1993, P425
[2]   CONSTRUCTION OF YEAST ARTIFICIAL CHROMOSOME LIBRARIES WITH LARGE INSERTS USING FRACTIONATION BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
ANAND, R ;
VILLASANTE, A ;
TYLERSMITH, C .
NUCLEIC ACIDS RESEARCH, 1989, 17 (09) :3425-3433
[3]   AN ORDERED COLLECTION OF BACILLUS-SUBTILIS DNA SEGMENTS CLONED IN YEAST ARTIFICIAL CHROMOSOMES [J].
AZEVEDO, V ;
ALVAREZ, E ;
ZUMSTEIN, E ;
DAMIANI, G ;
SGARAMELLA, V ;
EHRLICH, SD ;
SERROR, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (13) :6047-6051
[4]   PCR AMPLIFICATION OF UP TO 35-KB DNA WITH HIGH-FIDELITY AND HIGH-YIELD FROM LAMBDA-BACTERIOPHAGE TEMPLATES [J].
BARNES, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2216-2220
[5]   CLONING OF LARGE SEGMENTS OF EXOGENOUS DNA INTO YEAST BY MEANS OF ARTIFICIAL CHROMOSOME VECTORS [J].
BURKE, DT ;
CARLE, GF ;
OLSON, MV .
SCIENCE, 1987, 236 (4803) :806-812
[6]   EFFECTIVE AMPLIFICATION OF LONG TARGETS FROM CLONED INSERTS AND HUMAN GENOMIC DNA [J].
CHENG, S ;
FOCKLER, C ;
BARNES, WM ;
HIGUCHI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5695-5699
[7]   A 1ST-GENERATION PHYSICAL MAP OF THE HUMAN GENOME [J].
COHEN, D ;
CHUMAKOV, I ;
WEISSENBACH, J .
NATURE, 1993, 366 (6456) :698-701
[8]   A SEQUENCE ASSEMBLY AND EDITING PROGRAM FOR EFFICIENT MANAGEMENT OF LARGE PROJECTS [J].
DEAR, S ;
STADEN, R .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :3907-3911
[9]   HIGH-EFFICIENCY TRANSFORMATION OF ESCHERICHIA-COLI BY HIGH-VOLTAGE ELECTROPORATION [J].
DOWER, WJ ;
MILLER, JF ;
RAGSDALE, CW .
NUCLEIC ACIDS RESEARCH, 1988, 16 (13) :6127-6145
[10]  
ERRINGTON J, 1986, J GEN MICROBIOL, V132, P2953