High-throughput fingerprinting of bacterial artificial chromosomes using the SNaPshot labeling kit and sizing of restriction fragments by capillary electrophoresis

被引:183
作者
Luo, MC
Thomas, C
You, FM
Hsiao, J
Shu, OY
Buell, CR
Malandro, M
McGuire, PE
Anderson, OD
Dvorak, J [1 ]
机构
[1] Univ Calif Davis, Dept Agron & Range Sci, Davis, CA 95616 USA
[2] Inst Genomic Res, Rockville, MD 20850 USA
[3] Sagres Discovery, Davis, CA 95616 USA
[4] Univ Calif Davis, Genet Resources Conservat Program, Davis, CA 95616 USA
[5] USDA ARS, WRRC, GGD, Albany, CA 94710 USA
基金
美国国家科学基金会;
关键词
fingerprint; capillary electrophoresis; contig; physical mapping; BAC; multiple digestion; high-throughput; end labeling;
D O I
10.1016/S0888-7543(03)00128-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have developed an automated, high-throughput fingerprinting technique for large genomic DNA fragments suitable for the construction of physical maps of large genomes. In the technique described here, BAC DNA is isolated in a 96-well plate format and simultaneously digested with four 6-bp-recognizing restriction endonucleases that generate 3' recessed ends and one 4-bp-recognizing restriction endonuclease that generates a blunt end. Each of the four recessed 3' ends is labeled with a different fluorescent dye, and restriction fragments are sized on a capillary DNA analyzer. The resulting fingerprints are edited with a fingerprint-editing computer program and contigs are assembled with the FPC computer program. The technique was evaluated by repeated fingerprinting of several BACs included as controls in plates during routine fingerprinting of a BAC library and by reconstruction of contigs of rice BAC clones with known positions on rice chromosome 10. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:378 / 389
页数:12
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