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
[1]  
ASANO S, 1989, BIOCHEM INT, V19, P871
[2]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[3]   DNA METHYLATION INHIBITS TRANSCRIPTION INDIRECTLY VIA A METHYL-CPG BINDING-PROTEIN [J].
BOYES, J ;
BIRD, A .
CELL, 1991, 64 (06) :1123-1134
[4]   A SPECIFIC MISMATCH REPAIR EVENT PROTECTS MAMMALIAN-CELLS FROM LOSS OF 5-METHYLCYTOSINE [J].
BROWN, TC ;
JIRICNY, J .
CELL, 1987, 50 (06) :945-950
[5]   DIFFERENT BASE BASE MISPAIRS ARE CORRECTED WITH DIFFERENT EFFICIENCIES AND SPECIFICITIES IN MONKEY KIDNEY-CELLS [J].
BROWN, TC ;
JIRICNY, J .
CELL, 1988, 54 (05) :705-711
[6]  
BRUTLAG DL, 1980, ANNU REV GENET, V14, P122
[7]   DNA METHYLATION AND THE REGULATION OF GLOBIN GENE-EXPRESSION [J].
BUSSLINGER, M ;
HURST, J ;
FLAVELL, RA .
CELL, 1983, 34 (01) :197-206
[8]   DNA METHYLATION AND GENE ACTIVITY [J].
CEDAR, H .
CELL, 1988, 53 (01) :3-4
[9]   INFLUENCE OF CPG METHYLATION AND TARGET SPACING ON V(D)J RECOMBINATION IN A TRANSGENIC SUBSTRATE [J].
ENGLER, P ;
WENG, A ;
STORB, U .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) :571-577
[10]   COHABITATION OF SCAFFOLD BINDING REGIONS WITH UPSTREAM ENHANCER ELEMENTS OF 3 DEVELOPMENTALLY REGULATED GENES OF DROSOPHILA-MELANOGASTER [J].
GASSER, SM ;
LAEMMLI, UK .
CELL, 1986, 46 (04) :521-530