DNA METHYLATION AND EPIGENETIC INHERITANCE

被引:116
作者
HOLLIDAY, R
机构
[1] CSIRO Laboratory for Molecular Biology, North Ryde, New South Wales
关键词
D O I
10.1098/rstb.1990.0015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Classical genetics has revealed the mechanisms for the transmission of genes from generation to generation, but the strategy of the genes in unfolding the developmental programme remains obscure. Epigenetics comprises the study of the mechanisms that impart temporal and spatial control on the activities of all those genes required for the development of a complex organism from the zygote to the adult. Epigenetic changes in gene activity can be studied in relation to DNA methylation in cultured mammalian cells and it is also possible to isolate and characterize mutants with altered DNA methylase activity. Although this experimental system is quite far removed from the epigenetic controls acting during development it does provide the means to clarify the rules governing the silencing of genes by specific DNA methylation and their reactivation by demethylation. This in turn will facilitate studies on the control of gene expression in somatic cells of the developing organism or the adult. The general principles of epigenetic mechanisms can be defined. There are extreme contrasts between instability or switches in gene expression, such as those in stem-line cells, and the stable heritability of a specialized pattern of gene activities. In some situations cell lineages are known to be important, whereas in others coordinated changes in groups of cells have been demonstrated. Control of numbers of cell divisions and the size of organisms, or parts of organisms, is also essential. The epigenetic determination of gene expression can be reversed or reprogrammed in the germ line. The extent to which methylation or demethylation of specific DNA sequences can help explain these basic epigenetic mechanisms is briefly reviewed.
引用
收藏
页码:329 / 338
页数:10
相关论文
共 40 条
[1]   REACTIVATION OF X-LINKED GENES IN HUMAN-FIBROBLASTS TRANSFORMED BY ORIGIN-DEFECTIVE SV40 [J].
BEGGS, AH ;
AXELMAN, J ;
MIGEON, BR .
SOMATIC CELL AND MOLECULAR GENETICS, 1986, 12 (06) :585-594
[2]  
BORRELLO MG, 1987, CANCER RES, V47, P75
[3]   ADENOSINE KINASE AS A NEW SELECTIVE MARKER IN SOMATIC-CELL GENETICS - ISOLATION OF ADENOSINE KINASE-DEFICIENT MOUSE CELL LINES AND HUMAN-MOUSE HYBRID CELL LINES CONTAINING ADENOSINE KINASE [J].
CHAN, TS ;
CREAGAN, RP ;
REARDON, MP .
SOMATIC CELL GENETICS, 1978, 4 (01) :1-12
[4]   HUMAN-MOUSE SOMATIC HYBRID LINE SELECTED FOR HUMAN DEOXYCYTIDINE DEAMINASE [J].
CHAN, TS ;
LONG, C ;
GREEN, H .
SOMATIC CELL GENETICS, 1975, 1 (01) :81-90
[5]   COMPARTMENTS AND POLYCLONES IN INSECT DEVELOPMENT [J].
CRICK, FHC ;
LAWRENCE, PA .
SCIENCE, 1975, 189 (4200) :340-347
[6]  
Davidson E. H., 1986, GENE ACTIVITY EARLY, V3rd
[7]   STUDIES ON 1-BETA-D-ARABINOFURANOSYL-CYTOSINE (ARA-C) RESISTANT MUTANTS OF CHINESE-HAMSTER FIBROBLASTS .2. HIGH RESISTANCE TO ARA-C AS A GENETIC MARKER FOR CELLULAR HYBRIDIZATION [J].
DECHAMPS, M ;
DESAINTV.BR ;
EVRARD, C ;
SASSI, M ;
BUTTIN, G .
EXPERIMENTAL CELL RESEARCH, 1974, 86 (02) :269-279
[8]   HIGH-FREQUENCY REACTIVATION OF X-LINKED GENES IN CHINESE HAMSTERXHUMAN HYBRID-CELLS [J].
ELLIS, N ;
KEITGES, E ;
GARTLER, SM ;
ROCCHI, M .
SOMATIC CELL AND MOLECULAR GENETICS, 1987, 13 (03) :191-204
[9]  
ESPOSITO RE, 1968, GENETICS, V59, P191
[10]   INACTIVATION OF A TRANSFECTED GENE IN HUMAN-FIBROBLASTS CAN OCCUR BY DELETION, AMPLIFICATION, PHENOTYPIC SWITCHING, OR METHYLATION [J].
GEBARA, MM ;
DREVON, C ;
HARCOURT, SA ;
STEINGRIMSDOTTIR, H ;
JAMES, MR ;
BURKE, JF ;
ARLETT, CF ;
LEHMANN, AR .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (04) :1459-1464