ISOLATION OF GIANT DNA FRAGMENTS FROM FLOW-SORTED HUMAN-CHROMOSOMES

被引:31
作者
MINOSHIMA, S [1 ]
KAWASAKI, K [1 ]
FUKUYAMA, R [1 ]
MAEKAWA, M [1 ]
KUDOH, J [1 ]
SHIMIZU, N [1 ]
机构
[1] KEIO UNIV,DEPT MOLEC BIOL,35 SHINANOMACHI,SHINJUKU KU,TOKYO 160,JAPAN
来源
CYTOMETRY | 1990年 / 11卷 / 04期
关键词
Chromosome; 21; 22; NotI fragments; Pulsed field gel electrophoresis;
D O I
10.1002/cyto.990110413
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have established a method using a conventional cell sorter equipped with a single argon laser to sort intact human chromosomes that can be used as a source for the production of giant DNA fragments. Various improvements were made to both the equipment and sorting method to enhance the sorting resolution and avoid destruction of chromosomal DNA. Using this improved method chromosomes 21 and 22 were sorted from the B‐lymphoblastoid line GM00130B, digested with the rare cutting restriction endonuclease NotI, and analyzed by pulsed field gel electrophoresis followed by Southern hybridization using the Alu repetitive sequence as a probe. More than 25 discrete NotI giant DNA fragments ranging from 50 kb to longer than 2.5 Mb were separated and the size distribution pattern was unique for each chromosome, indicating successful sorting of intact chromosomes. The cumulative size of these Alu‐positive NotI DNA fragments were 22.7 Mb and 25.5 Mb for chromosomes 21 and 22, respectively. These values are 47% and 49% of the estimated size of chromosomes 21 (48 Mb) and 22 (52 Mb). Copyright © 1990 Wiley‐Liss, Inc.
引用
收藏
页码:539 / 546
页数:8
相关论文
共 26 条
[1]  
BARTRAM CR, 1984, BLOOD, V63, P223
[2]   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
[3]   SEPARATION OF CHROMOSOMAL DNA-MOLECULES FROM YEAST BY ORTHOGONAL-FIELD-ALTERNATION GEL-ELECTROPHORESIS [J].
CARLE, GF ;
OLSON, MV .
NUCLEIC ACIDS RESEARCH, 1984, 12 (14) :5647-5664
[4]   MEASUREMENT AND PURIFICATION OF HUMAN-CHROMOSOMES BY FLOW CYTOMETRY AND SORTING [J].
CARRANO, AV ;
GRAY, JW ;
LANGLOIS, RG ;
BURKHARTSCHULTZ, KJ ;
VANDILLA, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (03) :1382-1384
[5]   RAPID, SIMULTANEOUS MEASUREMENT OF DNA, PROTEIN, AND CELL VOLUME IN SINGLE CELLS FROM LARGE MAMMALIAN-CELL POPULATIONS [J].
CRISSMAN, HA ;
STEINKAMP, JA .
JOURNAL OF CELL BIOLOGY, 1973, 59 (03) :766-771
[6]   BASE SEQUENCE STUDIES OF 300 NUCLEOTIDE RENATURED REPEATED HUMAN DNA CLONES [J].
DEININGER, PL ;
JOLLY, DJ ;
RUBIN, CM ;
FRIEDMANN, T ;
SCHMID, CW .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 151 (01) :17-33
[7]   NUCLEOTIDE-SEQUENCE OF THE SIMIAN SARCOMA-VIRUS GENOME - DEMONSTRATION THAT ITS ACQUIRED CELLULAR SEQUENCES ENCODE THE TRANSFORMING GENE-PRODUCT P28SIS [J].
DEVARE, SG ;
REDDY, EP ;
LAW, JD ;
ROBBINS, KC ;
AARONSON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (03) :731-735
[8]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[9]   FRACTIONATION OF LARGE MAMMALIAN DNA RESTRICTION FRAGMENTS USING VERTICAL PULSED-FIELD GRADIENT GEL-ELECTROPHORESIS [J].
GARDINER, K ;
LAAS, W ;
PATTERSON, D .
SOMATIC CELL AND MOLECULAR GENETICS, 1986, 12 (02) :185-195
[10]   HIGH-SPEED CHROMOSOME SORTING [J].
GRAY, JW ;
DEAN, PN ;
FUSCOE, JC ;
PETERS, DC ;
TRASK, BJ ;
VANDENENGH, GJ ;
VANDILLA, MA .
SCIENCE, 1987, 238 (4825) :323-329