CLONING AND CHARACTERIZATION OF EAGI YACS FROM HUMAN CHROMOSOME-21

被引:6
作者
GINGRICH, JC
LOWRY, SR
KUO, WL
GRAY, J
SMITH, CL
CANTOR, CR
机构
[1] LAWRENCE BERKELEY LAB,DIV CHEM BIODYNAM,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,DEPT MOLEC & CELL BIOL,BERKELEY,CA 94720
[3] UNIV CALIF SAN FRANCISCO,DEPT LAB MED,SAN FRANCISCO,CA 94143
关键词
D O I
10.1006/geno.1993.1043
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
Yeast artificial chromosomes (YACs) were made from a total EagI digest of DNA from a mouse-human chromosome 21 hybrid cell line. Approximately 3750 YACs, corresponding to 75-125 human YACs, with an average size of approximately 100 kb were recovered. Southern hybridization indicates that the chimera frequency in this library may be less than 3%. Thirty-four of the human Eag I YACs were regionally assigned by a number of methods. Some YACs were regionally assigned to one of six chromosome regions by hybridization of Alu -PCR products from the YAC against Alu-PCR-amplified DNA from a panel of hybrid cell lines that contain various parts of chromosome 21. Additional YACs were regionally assigned by fluorescence in situ hybridization using either biotinylated Alu-PCR products or yeast genomic DNA from the YAC-containing strains as probes. The regionally assigned Eag I YACs are located preferentially in two regions of the chromosome: near the q telomere and in the p-arm ribosomal gene region. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:228 / 230
页数:3
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