A human chromosome 22 Fosmid resource: Mapping and analysis of 96 clones

被引:6
作者
Birren, BW
TachiIri, Y
Kim, UJ
Nguyen, M
Shizuya, H
Korenberg, JR
Simon, MI
机构
[1] UNIV CALIF LOS ANGELES,CEDARS SINAI MED CTR,AHMANSON DEPT PEDIAT,CTR MED GENET BIRTH DEFECTS,LOS ANGELES,CA 90048
[2] CALTECH,DIV BIOL 14775,PASADENA,CA 91125
[3] HAMAMATSU PHOTON KK,CENT RES LAB,RES GRP 8,HAMAKITA,SHIZUOKA 434,JAPAN
关键词
D O I
10.1006/geno.1996.0246
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 created a resource for chromosome 22 consisting of 96 unique, well-characterized Fosmids, The Fosmid vector permits efficient cloning of DNA fragments averaging 40 kb in a single-copy vector based on the F factor of Escherichia coli, We have found that Fosmid clones from human chromosome 22 show remarkable stability and are useful for a wide variety of applications in genome analysis, These 96 clones have been localized by FISH, using high-resolution fluorescent banding and multicolor mapping techniques, and their position on the chromosome was correlated with their content of a number of common repeated sequence elements, We identified a subset of clones likely to contain genes by restriction analysis using the enzymes NotI, MluI, SacII, and BssHII, This collection of cytogenetically anchored clones, representing nearly 7% of the chromosome, is of immediate value for detecting chromosomal rearrangements, for use in gene isolation, and as a framework for physical mapping. (C) 1996 Academic Press, Inc.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 39 条
[1]   A HUMAN-SPECIFIC SUBFAMILY OF ALU-SEQUENCES [J].
BATZER, MA ;
DEININGER, PL .
GENOMICS, 1991, 9 (03) :481-487
[2]  
BELL CJ, 1995, HUM MOL GENET, V4, P59
[3]   CPG ISLANDS AS GENE MARKERS IN THE VERTEBRATE NUCLEUS [J].
BIRD, AP .
TRENDS IN GENETICS, 1987, 3 (12) :342-347
[4]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[5]   SEQUENCE AND ANALYSIS OF THE HUMAN ABL GENE, THE BCR GENE, AND REGIONS INVOLVED IN THE PHILADELPHIA CHROMOSOMAL TRANSLOCATION [J].
CHISSOE, SL ;
BODENTEICH, A ;
WANG, YF ;
WANG, YP ;
BURIAN, D ;
CLIFTON, SW ;
CRABTREE, J ;
FREEMAN, A ;
IYER, K ;
LI, JA ;
MA, YC ;
MCLAURY, HJ ;
PAN, HQ ;
SARHAN, OH ;
TOTH, S ;
WANG, ZL ;
ZHANG, GZ ;
HEISTERKAMP, N ;
GROFFEN, J ;
ROE, BA .
GENOMICS, 1995, 27 (01) :67-82
[6]   A SURVEY OF THE GENOMIC DISTRIBUTION OF ALPHA-SATELLITE DNA ON ALL THE HUMAN-CHROMOSOMES, AND DERIVATION OF A NEW CONSENSUS SEQUENCE [J].
CHOO, KH ;
VISSEL, B ;
NAGY, A ;
EARLE, E ;
KALITSIS, P .
NUCLEIC ACIDS RESEARCH, 1991, 19 (06) :1179-1182
[7]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[8]   A 1ST-GENERATION PHYSICAL MAP OF THE HUMAN GENOME [J].
COHEN, D ;
CHUMAKOV, I ;
WEISSENBACH, J .
NATURE, 1993, 366 (6456) :698-701
[9]   THE HUMAN THE-LTR(O) AND MSTII INTERSPERSED REPEATS ARE SUBFAMILIES OF A SINGLE WIDELY DISTRIBUTED HIGHLY VARIABLE REPEAT FAMILY [J].
FIELDS, CA ;
GRADY, DL ;
MOYZIS, RK .
GENOMICS, 1992, 13 (02) :431-436
[10]   DEFINING THE BEGINNING AND END OF KPNI FAMILY SEGMENTS [J].
GRIMALDI, G ;
SKOWRONSKI, J ;
SINGER, MF .
EMBO JOURNAL, 1984, 3 (08) :1753-1759