Epigenetic alterations in aging

被引:169
作者
Gonzalo, Susana [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, Radiat & Canc Biol Div, St Louis, MO 63108 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63108 USA
关键词
cancer; epigenetic changes; A-TYPE LAMINS; DNA METHYLATION; LIFE-SPAN; HISTONE METHYLATION; GENOMIC INSTABILITY; GENE-EXPRESSION; CHROMATIN MODIFICATIONS; PROMOTER METHYLATION; MICRORNA EXPRESSION; CANCER-CELLS;
D O I
10.1152/japplphysiol.00238.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Gonzalo S. Epigenetic alterations in aging. J Appl Physiol 109: 586-597, 2010. First published May 6, 2010; doi: 10.1152/japplphysiol.00238.2010.-Aging is a multifaceted process characterized by genetic and epigenetic changes in the genome. The genetic component of aging received initially all of the attention. Telomere attrition and accumulation of mutations due to a progressive deficiency in the repair of DNA damage with age remain leading causes of genomic instability. However, epigenetic mechanisms have now emerged as key contributors to the alterations of genome structure and function that accompany aging. The three pillars of epigenetic regulation are DNA methylation, histone modifications, and noncoding RNA species. Alterations of these epigenetic mechanisms affect the vast majority of nuclear processes, including gene transcription and silencing, DNA replication and repair, cell cycle progression, and telomere and centromere structure and function. Here, we summarize the lines of evidence indicating that these epigenetic defects might represent a major factor in the pathophysiology of aging and aging-related diseases, especially cancer.
引用
收藏
页码:586 / 597
页数:12
相关论文
共 138 条
[1]   Polycomb Mediated Epigenetic Silencing and Replication Timing at the INK4a/ARF Locus during Senescence [J].
Agherbi, Hanane ;
Gaussmann-Wenger, Anne ;
Verthuy, Christophe ;
Chasson, Lionel ;
Serrano, Manuel ;
Djabali, Malek .
PLOS ONE, 2009, 4 (05)
[2]  
Ahuja N, 1998, CANCER RES, V58, P5489
[3]   Developmentally regulated piRNA clusters implicate MILI in transposon control [J].
Aravin, Alexei A. ;
Sachidanandam, Ravi ;
Girard, Angelique ;
Fejes-Toth, Katalin ;
Hannon, Gregory J. .
SCIENCE, 2007, 316 (5825) :744-747
[4]   Methyl-CpG-binding proteins in cancer: blaming the DNA methylation messenger [J].
Ballestar, E ;
Esteller, M .
BIOCHEMISTRY AND CELL BIOLOGY, 2005, 83 (03) :374-384
[5]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[6]   Suv4-20h deficiency results in telomere elongation and derepression of telomere recombination [J].
Benetti, Roberta ;
Gonzalo, Susana ;
Jaco, Isobel ;
SChotta, Gunnar ;
Klatt, Peter ;
Jenuwein, Thomas ;
Blasco, Maria A. .
JOURNAL OF CELL BIOLOGY, 2007, 178 (06) :925-936
[7]   The complex language of chromatin regulation during transcription [J].
Berger, Shelley L. .
NATURE, 2007, 447 (7143) :407-412
[8]   An operational definition of epigenetics [J].
Berger, Shelley L. ;
Kouzarides, Tony ;
Shiekhattar, Ramin ;
Shilatifard, Ali .
GENES & DEVELOPMENT, 2009, 23 (07) :781-783
[9]   The mammalian epigenome [J].
Bernstein, Bradley E. ;
Meissner, Alexander ;
Lander, Eric S. .
CELL, 2007, 128 (04) :669-681
[10]   MiR-15a and MiR-16 Control Bmi-1 Expression in Ovarian Cancer [J].
Bhattacharya, Resham ;
Nicoloso, Milena ;
Arvizo, Rochelle ;
Wang, Enfeng ;
Cortez, Angelica ;
Rossi, Simona ;
Calin, George A. ;
Mukherjee, Priyabrata .
CANCER RESEARCH, 2009, 69 (23) :9090-9095