MECHANISMS FOR METHYLATION-MEDIATED GENE SILENCING AND AGING

被引:14
作者
TOLLEFSBOL, TO [1 ]
ANDREWS, LG [1 ]
机构
[1] DUKE UNIV, MED CTR, DEPT MICROBIOL & IMMUNOL, DURHAM, NC 27710 USA
关键词
D O I
10.1016/0306-9877(93)90040-W
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Gene silencing is often mediated by CpG methylation of key protein binding sites within gene regulatory sequences (GRSs). An aging mechanism is proposed based on this gene-silencing phenomenon whereby accumulation over time of methylation within GRSs contributes to cellular senescence. The proposed molecular mechanism for age-related gene silencing is the spreading of methylation through the regulatory sequences of genes resulting in progressive reduction of gene transcription. There is considerable experimental evidence for methylation spreading and its role in gene silencing, but the mechanism responsible for this process has not been elucidated. A four-step mechanism is proposed whereby an original methylation occurs, methyltransferase (MTase) molecules progressively move 5' to 3' from this site, neighboring CpG dinucleotides become methylated, and diminished gene expression ensues. Over time, this process may lead to widespread gene silencing in diverse dividing and nondividing cell types contributing to aging of the organism.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 55 条
[1]   DNA METHYLATION - THE EFFECT OF MINOR BASES ON DNA PROTEIN INTERACTIONS [J].
ADAMS, RLP .
BIOCHEMICAL JOURNAL, 1990, 265 (02) :309-320
[2]   GENOMIC FOOTPRINTING REVEALS CELL TYPE SPECIFIC DNA-BINDING OF UBIQUITOUS FACTORS [J].
BECKER, PB ;
RUPPERT, S ;
SCHUTZ, G .
CELL, 1987, 51 (03) :435-443
[3]  
BENVENISTY N, 1989, J ROY COLL PHYS LOND, V23, P156
[4]   GROWTH-DEPENDENT EXPRESSION OF MULTIPLE SPECIES OF DNA METHYLTRANSFERASE IN MURINE ERYTHROLEUKEMIA-CELLS [J].
BESTOR, TH ;
INGRAM, VM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2674-2678
[5]   2 DNA METHYLTRANSFERASES FROM MURINE ERYTHROLEUKEMIA-CELLS - PURIFICATION, SEQUENCE SPECIFICITY, AND MODE OF INTERACTION WITH DNA [J].
BESTOR, TH ;
INGRAM, VM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (18) :5559-5563
[6]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[7]  
BOLDEN A, 1984, J BIOL CHEM, V259, P2437
[8]   THE PRIMARY DNA-SEQUENCE DETERMINES INVITRO METHYLATION BY MAMMALIAN DNA METHYLTRANSFERASES [J].
BOLDEN, AH ;
WARD, CA ;
NALIN, CM ;
WEISSBACH, A .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, 1986, 33 :231-250
[9]   DNA METHYLATION INHIBITS TRANSCRIPTION INDIRECTLY VIA A METHYL-CPG BINDING-PROTEIN [J].
BOYES, J ;
BIRD, A .
CELL, 1991, 64 (06) :1123-1134
[10]  
CARBONE AM, 1988, J IMMUNOL, V141, P1369