Involvement of DNA methylation in binding of a highly repetitive DNA component to nuclear scaffold proteins from rat liver

被引:13
作者
Hibino, Y
Ohzeki, H
Hirose, N
Morita, Y
Sugano, N
机构
[1] Toyama Med & Pharmaceut Univ, Mol Genet Res Ctr, Toyama 9300194, Japan
[2] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Toyama 9300194, Japan
关键词
D O I
10.1006/bbrc.1998.9620
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Experimental reduction of the amount of CpG methylation in a highly repetitive DNA component was achieved by growth of Ac2F cells in the presence of 5-aza-2'-deoxycytidine or procainamide, as judged by the results of methyl-sensitive restriction endonuclease digestion and colony hybridization. Modification of genomic DNA with these DNA methylation inhibitors increased the release of 370-bp highly repetitive DNA from rat chromosomal DNA by HindIII digestion. This result indicated that highly repetitive DNA components in the nuclear scaffold fraction are hypermethylated. On the other hand, methylated DNA was used for southwestern analysis to investigate the protein(s) which bind specifically to the DNA in the nuclear scaffold fraction. The introduction of additional methylated cytosines within a highly repetitive DNA component affected the binding of DNA to the nuclear scaffold proteins. Thus, cytosine methylation may be involved in the regulation of gene expression and construction of the higher-order structure of chromatin. (C) 1998 Academic Press.
引用
收藏
页码:296 / 301
页数:6
相关论文
共 45 条
[31]   DISSECTION OF THE METHYL-CPG BINDING DOMAIN FROM THE CHROMOSOMAL PROTEIN MECP2 [J].
NAN, XS ;
MEEHAN, RR ;
BIRD, A .
NUCLEIC ACIDS RESEARCH, 1993, 21 (21) :4886-4892
[32]   MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin [J].
Nan, XS ;
Campoy, FJ ;
Bird, A .
CELL, 1997, 88 (04) :471-481
[33]   Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex [J].
Nan, XS ;
Ng, HH ;
Johnson, CA ;
Laherty, CD ;
Turner, BM ;
Eisenman, RN ;
Bird, A .
NATURE, 1998, 393 (6683) :386-389
[34]   POLYMERASE CHAIN REACTION-AIDED GENOMIC SEQUENCING OF AN X-CHROMOSOME-LINKED CPG ISLAND - METHYLATION PATTERNS SUGGEST CLONAL INHERITANCE, CPG SITE AUTONOMY, AND AN EXPLANATION OF ACTIVITY STATE STABILITY [J].
PFEIFER, GP ;
STEIGERWALD, SD ;
HANSEN, RS ;
GARTLER, SM ;
RIGGS, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8252-8256
[35]   CURVATURE OF MOUSE SATELLITE DNA AND CONDENSATION OF HETEROCHROMATIN [J].
RADIC, MZ ;
LUNDGREN, K ;
HAMKALO, BA .
CELL, 1987, 50 (07) :1101-1108
[36]   DNA METHYLATION AND GENOMIC IMPRINTING [J].
RAZIN, A ;
CEDAR, H .
CELL, 1994, 77 (04) :473-476
[37]   SIMILARITY OF DNA SEQUENCES REMAINING BOUND TO SCAFFOLD UPON NUCLEASE TREATMENT OF INTERPHASE NUCLEI AND METAPHASE CHROMOSOMES [J].
RAZIN, SV ;
MANTIEVA, VL ;
GEORGIEV, GP .
NUCLEIC ACIDS RESEARCH, 1979, 7 (06) :1713-1735
[38]  
Sambrook J., 1989, MOL CLONING, V2, P1
[39]   CHARACTERIZATION OF A HIGHLY REPETITIVE SEQUENCE DNA FAMILY IN RAT [J].
SEALY, L ;
HARTLEY, J ;
DONELSON, J ;
CHALKLEY, R ;
HUTCHISON, N ;
HAMKALO, B .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 145 (02) :291-318
[40]   HIGH-FREQUENCY MUTAGENESIS BY A DNA METHYLTRANSFERASE [J].
SHEN, JC ;
RIDEOUT, WM ;
JONES, PA .
CELL, 1992, 71 (07) :1073-1080