PREFERENTIAL ISOLATION OF DNA FRAGMENTS ASSOCIATED WITH CPG ISLANDS

被引:22
作者
SHIRAISHI, M [1 ]
LERMAN, LS [1 ]
SEKIYA, T [1 ]
机构
[1] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
关键词
DENATURING GRADIENT GEL ELECTROPHORESIS; STRAND DISSOCIATION KINETICS; GENE IDENTIFICATION;
D O I
10.1073/pnas.92.10.4229
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We describe a procedure for preferential isolation of DNA fragments with G+C-rich portions. Such fragments occur in known genes within or adjacent to CpG islands. Since about 56% of human genes are associated with CpG islands, isolation of these fragments permits detection and probing of many genes within much larger segments of DNA, such as cosmids or yeast artificial chromosomes, which have not been sequenced, Cloned DNA fragments digested with four restriction endonucleases were subjected to denaturing gradient gel electrophoresis. Long G+C-rich sections in fragments inhibit strand dissociation after the fragments reach retardation level in the gradient; such fragments are retained in the gel after most others disappear. Nucleotide sequences of the retained fragments show that about half of these fragments appear to be derived from CpG islands, Northern analysis indicated the presence of RNA complementary to most of the retained fragments. A heuristic approach to the relation between base sequence and the kinetics of strand dissociation of partly melted molecules appears to account for retention and nonretention. The expectation that CpG island fragments will be enriched among fragments retained in a denaturing gradient is supported by rate estimates based on melting theory applied to known sequences, This method, designated SPM for segregation of partly melted molecules, is expected to provide a means for convenient and efficient isolation of genes from unsequenced DNA.
引用
收藏
页码:4229 / 4233
页数:5
相关论文
共 18 条
[1]  
ABRAMS ES, 1992, METHOD ENZYMOL, V212, P71
[2]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[3]  
BICKMORE WA, 1992, METHOD ENZYMOL, V216, P224
[4]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[5]   EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING [J].
BUCKLER, AJ ;
CHANG, DD ;
GRAW, SL ;
BROOK, JD ;
HABER, DA ;
SHARP, PA ;
HOUSMAN, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :4005-4009
[6]   PURIFICATION OF CPG ISLANDS USING A METHYLATED DNA-BINDING COLUMN [J].
CROSS, SH ;
CHARLTON, JA ;
NAN, XS ;
BIRD, AP .
NATURE GENETICS, 1994, 6 (03) :236-244
[7]   EXON TRAPPING - A GENETIC SCREEN TO IDENTIFY CANDIDATE TRANSCRIBED SEQUENCES IN CLONED MAMMALIAN GENOMIC DNA [J].
DUYK, GM ;
KIM, SW ;
MYERS, RM ;
COX, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8995-8999
[8]   CPG ISLANDS IN VERTEBRATE GENOMES [J].
GARDINERGARDEN, M ;
FROMMER, M .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 196 (02) :261-282
[9]   IDENTIFICATION OF GENES WITHIN CPG-ENRICHED DNA FROM HUMAN-CHROMOSOME 4P16.3 [J].
JOHN, RM ;
ROBBINS, CA ;
MYERS, RM .
HUMAN MOLECULAR GENETICS, 1994, 3 (09) :1611-1616
[10]   CPG ISLANDS AS GENE MARKERS IN THE HUMAN GENOME [J].
LARSEN, F ;
GUNDERSEN, G ;
LOPEZ, R ;
PRYDZ, H .
GENOMICS, 1992, 13 (04) :1095-1107