CHROMOSOMAL ASSIGNMENT OF HUMAN YAC CLONES BY FLUORESCENCE INSITU HYBRIDIZATION - USE OF SINGLE-YEAST-COLONY PCR AND MULTIPLE LABELING

被引:64
作者
BALDINI, A
ROSS, M
NIZETIC, D
VATCHEVA, R
LINDSAY, EA
LEHRACH, H
SINISCALCO, M
机构
[1] CNR,IST GENET MOLEC,PORTO CONTE RES & TRAINING LABS,ALGHERO,ITALY
[2] ST MARKS HOSP,DEPT BIOCHEM & MOLEC GENET,LONDON EC1V 2PS,ENGLAND
关键词
D O I
10.1016/S0888-7543(05)80303-9
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
Alu-PCR provides a convenient tool for amplification of human-specific sequences from yeast DNA containing yeast artificial chromosomes (YAC) clones. PCR products can be labeled nonisotopically and hybridized in situ, and the chromosomal origin of the clones can be determined. This avoids time-consuming gel purification of the yeast artificial chromosome and the low-efficiency procedure of labeling whole yeast DNA containing the YAC. The application of Alu-PCR to single-yeast colonies permits the mapping of YACs at a very early stage of their characterization. In situ hybridization can detect clones with noncontiguous fragments of DNA, and these can be discarded without further time-consuming characterization. To increase further the potential of the method, we show the application of multicolor hybridization techniques. © 1992 Academic Press, Inc. All rights reserved.
引用
收藏
页码:181 / 184
页数:4
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