Impacts of transcriptional regulation on aging and senescence

被引:58
作者
Roy, AK
Oh, T
Rivera, O
Mubiru, J
Song, CS
Chatterjee, B
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[2] S Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA
关键词
transcription factors; aging; gene regulation; senescence phenotype; reactive oxygen species;
D O I
10.1016/S1568-1637(02)00006-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The genetic makeup of the organism appears to dictate the species-specific rate of aging and the maximum life-span potential. The genotype is converted to phenotype through transcriptional and translational regulation. A group of gene regulatory proteins (transcription factors) play critical roles in controlling the rates of transcription of specific genes by directly interacting with regulatory sequences at gene promoters. Here, we review the basic mechanism of transcriptional control and the role of a number of transcription factors whose level and/or activity alter with age. Among these age-dependent transcription factors, many are involved in the regulation of stress and inflammatory responses and are subjected to functional alterations by reactive oxygen species (ROSs). A progressive rise of oxidative stress, impaired ability to cope with stressful stimuli and prolongation of the inflammatory response are some of the hallmarks of the senescent phenotype. Results published to date are supportive of the concept that a species-specific program of the temporal regulation of genes with additional modulation by a number of epigenetic factors, mediates the age-dependent deterioration of physiological functions and development of the senescent phenotype. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:367 / 380
页数:14
相关论文
共 80 条
[1]  
AMMENDOLA R, 1992, J BIOL CHEM, V267, P17944
[2]   THE DNA-BINDING EFFICIENCY OF SP1 IS AFFECTED BY REDOX CHANGES [J].
AMMENDOLA, R ;
MESURACA, M ;
RUSSO, T ;
CIMINO, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 225 (01) :483-489
[3]  
An MR, 1996, MOL CELL BIOL, V16, P2295
[4]   TRANSCRIPTION FACTOR LOADING ON THE MMTV PROMOTER - A BIMODAL MECHANISM FOR PROMOTER ACTIVATION [J].
ARCHER, TK ;
LEFEBVRE, P ;
WOLFORD, RG ;
HAGER, GL .
SCIENCE, 1992, 255 (5051) :1573-1576
[5]   NF-kappa B: Ten years after [J].
Baeuerle, PA ;
Baltimore, D .
CELL, 1996, 87 (01) :13-20
[6]   The CBP co-activator is a histone acetyltransferase [J].
Bannister, AJ ;
Kouzarides, T .
NATURE, 1996, 384 (6610) :641-643
[7]   Acetylation of p53 activates transcription through recruitment of coactivators/histone acetyltransferases [J].
Barlev, NA ;
Liu, L ;
Chehab, NH ;
Mansfield, K ;
Harris, KG ;
Halazonetis, TD ;
Berger, SL .
MOLECULAR CELL, 2001, 8 (06) :1243-1254
[8]   Hormone activation induces nucleosome positioning in vivo [J].
Belikov, S ;
Gelius, B ;
Almouzni, G ;
Wrange, Ö .
EMBO JOURNAL, 2000, 19 (05) :1023-1033
[9]   Interaction of human apurinic endonuclease and DNA polymerase beta in the base excision repair pathway [J].
Bennett, RAO ;
Wilson, DM ;
Wong, D ;
Demple, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7166-7169
[10]  
Berger Shelley L., 2001, Molecular Cell, V8, P263, DOI 10.1016/S1097-2765(01)00330-6