Gene expression profile of long-lived snell dwarf mice

被引:33
作者
Dozmorov, I
Galecki, A
Chang, YY
Krzesicki, R
Vergara, M
Miller, RA
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Geriatr Ctr, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Ann Arbor VA Med Ctr, Ann Arbor, MI 48109 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2002年 / 57卷 / 03期
关键词
D O I
10.1093/gerona/57.3.B99
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
To gain further insight into the basis for the extended longevity and delayed aging of Snell dwarf (dw/dw) mice, we have measured levels of expression of 2352 genes in liver of mice at 6 months of age. We find 60 genes for the which the Student's t statistic meets the arbitrary criterion of p < .001, and among these 17 meet the Bonferroni-adjusted significance criterion at p < .05, which corresponds to a nominal value of p < .00002. Using the Bonferroni criterion. we find that dwarf mice show increases in liver mRNA for two mannose-binding lectins, two DNA binding protein,,, serum amyloid P component. corticosteroid-binding globulin. and insulin-like growth factor -binding protein 2, as well as decreases in a two phosphodiesterases. a pheromone-binding urinary protein, insulin-like growth factor-I (IGF-I). a calcium-binding protein calgranulin B, a deubiquitinating enzyme. a hydroxysteroid dehydrogenase, a DNA methyltransferase, a glycine transporter, ania placental lactogen. We also use this data set to compare the results of different suggested criteria for evaluating intergroup differences in gene expression. Of the 2352 genes examined, 524 (22%) showed a twofold difference between dwarf and normal mice. but most of these fail to meet the conventional significance criterion of p < .05, let alone criteria C that have been adjusted to compensate for multiple comparison artifacts. The list of genes that show reliable differences between dwarf and control animals provides new insights into the C range of changes induced by deficiencies in growth hormone, thyroid-stimulating hormone. and prolactin, and it will help to guide further studies of the pathways by which these hormone defic- ciencies contribute to delayed aging in these mutant mice.
引用
收藏
页码:B99 / B108
页数:10
相关论文
共 18 条
[1]  
Bartke A, 2000, RES PRO CEL, V29, P181
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   Dwarf mice and the ageing process [J].
BrownBorg, HM ;
Borg, KE ;
Meliska, CJ ;
Bartke, A .
NATURE, 1996, 384 (6604) :33-33
[4]   Microarray expression profiling identifies genes with altered expression in HDL-deficient mice [J].
Callow, MJ ;
Dudoit, S ;
Gong, EL ;
Speed, TP ;
Rubin, EM .
GENOME RESEARCH, 2000, 10 (12) :2022-2029
[5]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[6]   Assessment of growth parameters and life span of GHR/BP gene-disrupted mice [J].
Coschigano, KT ;
Clemmons, D ;
Bellush, LL ;
Kopchick, JJ .
ENDOCRINOLOGY, 2000, 141 (07) :2608-2613
[7]  
DUDOIT S, 2000, STAT METHODS IDENTIF
[8]   INSULIN-LIKE GROWTH FACTOR-I LEVELS IN PROPORTIONATE DOGS, CHONDRODYSTROPHIC DOGS AND IN GIANT DOGS [J].
EIGENMANN, JE ;
AMADOR, A ;
PATTERSON, DF .
ACTA ENDOCRINOLOGICA, 1988, 118 (01) :105-108
[9]   BODY SIZE PARALLELS INSULIN-LIKE GROWTH FACTOR-I LEVELS BUT NOT GROWTH-HORMONE SECRETORY CAPACITY [J].
EIGENMANN, JE ;
PATTERSON, DF ;
FROESCH, ER .
ACTA ENDOCRINOLOGICA, 1984, 106 (04) :448-453
[10]   Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production [J].
Flurkey, K ;
Papaconstantinou, J ;
Miller, RA ;
Harrison, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6736-6741