AGE-RELATED INCREASES IN GLIAL FIBRILLARY ACIDIC PROTEIN DO NOT SHOW PROPORTIONATE CHANGES IN TRANSCRIPTION RATES OR DNA METHYLATION IN THE CEREBRAL-CORTEX AND HIPPOCAMPUS OF MALE-RATS

被引:18
作者
LAPING, NJ
TETER, B
ANDERSON, CP
OSTERBURG, HH
OCALLAGHAN, JP
JOHNSON, SA
FINCH, CE
机构
[1] SMITHKLINE BEECHAM PHARMACEUT, DEPT RENAL PHARMACOL, KING OF PRUSSIA, PA 19406 USA
[2] UNIV SO CALIF, ETHEL PERCY ANDRUS GERONTOL CTR, DIV NEUROGERONTOL, LOS ANGELES, CA 90089 USA
[3] UNIV SO CALIF, DEPT BIOL SCI, LOS ANGELES, CA 90089 USA
[4] CORTEX PHARMACEUT INC, IRVINE, CA USA
[5] US EPA, DIV NEUROTOXICOL, RES TRIANGLE PK, NC 27711 USA
关键词
GLIAL FIBRILLARY ACIDIC PROTEIN; AGE-RELATED INCREASES; DNA METHYLATION; RAT CEREBRAL CORTEX; RAT HIPPOCAMPUS; TRANSCRIPTION RATES;
D O I
10.1002/jnr.490390612
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Age-related increases in the expression of glial fibrillary acidic protein (GFAP) in many brain regions are observed in short- and long-lived mammals, Possible genomic mechanisms for the increase of GFAP mRNA and protein were studied in the hippocampus and cortex of male F344 rats and a longer-lived hybrid F-1 (F344 x Brown Norway), No age-related changes were found in the extent of cytosine methylation at 19 CpG sites in the 5'-upstream GFAP promoter and in exon 1, With the nuclear runon assay, no change was found in the transcription rate of GFAP in the cerebral cortex or hippocampus, Thus, age-related increases in GFAP are not associated with proportionate changes in transcription rates or DNA methylation, However, the transcription of glutamine synthetase was increased by about 60%. These findings contrast with age-related loss of bulk tissue DNA methylation and decreased transcription rates of other genes reported in non-neural tissues. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:710 / 717
页数:8
相关论文
共 60 条
  • [1] DYNAMICS OF DNA METHYLATION DURING DEVELOPMENT
    BRANDEIS, M
    ARIEL, M
    CEDAR, H
    [J]. BIOESSAYS, 1993, 15 (11) : 709 - 713
  • [2] GFAP PROMOTER DIRECTS ASTROCYTE-SPECIFIC EXPRESSION IN TRANSGENIC MICE
    BRENNER, M
    KISSEBERTH, WC
    SU, Y
    BESNARD, F
    MESSING, A
    [J]. JOURNAL OF NEUROSCIENCE, 1994, 14 (03) : 1030 - 1037
  • [3] Bronson R., 1990, GENETIC EFFECTS AGIN, VII, P279
  • [4] AGE-RELATED GLIOSIS IN THE WHITE MATTER OF MICE
    BRONSON, RT
    LIPMAN, RD
    HARRISON, DE
    [J]. BRAIN RESEARCH, 1993, 609 (1-2) : 124 - 128
  • [5] METHYLATION AND EXPRESSION OF NEUROFILAMENT GENES IN TISSUES AND IN CELL-LINES OF THE MOUSE
    BRUCE, J
    SCHWARTZ, ML
    SHNEIDMAN, PS
    SCHLAEPFER, WW
    [J]. MOLECULAR BRAIN RESEARCH, 1993, 17 (3-4): : 269 - 278
  • [6] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [7] BRAIN POLY(A)RNA DURING AGING - STABILITY OF YIELD AND SEQUENCE COMPLEXITY IN 2 RAT STRAINS
    COLMAN, PD
    KAPLAN, BB
    OSTERBURG, HH
    FINCH, CE
    [J]. JOURNAL OF NEUROCHEMISTRY, 1980, 34 (02) : 335 - 345
  • [8] COONEY CA, 1993, GROWTH DEVELOP AGING, V57, P261
  • [9] DAS BR, 1989, BIOCHEM ARCH, V5, P359
  • [10] NEURON ATROPHY DURING AGING - PROGRAMMED OR SPORADIC
    FINCH, CE
    [J]. TRENDS IN NEUROSCIENCES, 1993, 16 (03) : 104 - 110