Age-associated alteration of gene expression patterns in mouse oocytes

被引:416
作者
Hamatani, T [1 ]
Falco, G [1 ]
Akutsu, H [1 ]
Stagg, CA [1 ]
Sharov, AA [1 ]
Dudekula, DB [1 ]
VanBuren, V [1 ]
Ko, MSH [1 ]
机构
[1] NIA, Dev Genom & Aging Sect, Genet Lab, NIH, Baltimore, MD 21224 USA
关键词
D O I
10.1093/hmg/ddh241
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Decreasing oocyte competence with maternal aging is a major factor in human infertility. To investigate the age-dependent molecular changes in a mouse model, we compared the expression profiles of metaphase II oocytes collected from 5- to 6-week-old mice with those collected from 42- to 45-week-old mice using the NIA 22K 60-mer oligo microarray. Among approximately 11 000 genes whose transcripts were detected in oocytes, about 5% (530) showed statistically significant expression changes, excluding the possibility of global decline in transcript abundance. Consistent with the generally accepted view of aging, the differentially expressed genes included ones involved in mitochondrial function and oxidative stress. However, the expression of other genes involved in chromatin structure, DNA methylation, genome stability and RNA helicases was also altered, suggesting the existence of additional mechanisms for aging. Among the transcripts decreased with aging, we identified and characterized a group of new oocyte-specific genes, members of the human NACHT, leucine-rich repeat and PYD-containing (NALP) gene family. These results have implications for aging research as well as for clinical ooplasmic donation to rejuvenate aging oocytes.
引用
收藏
页码:2263 / 2278
页数:16
相关论文
共 102 条
[61]   Comparing genomic expression patterns across species identifies shared transcriptional profile in aging [J].
McCarroll, SA ;
Murphy, CT ;
Zou, SG ;
Pletcher, SD ;
Chin, CS ;
Jan, YN ;
Kenyon, C ;
Bargmann, CI ;
Li, H .
NATURE GENETICS, 2004, 36 (02) :197-204
[62]  
Meirelles FV, 1997, GENETICS, V145, P445
[63]   Golgi apparatus dynamics during mouse oocyte in vitro maturation: Effect of the membrane trafficking inhibitor brefeldin A [J].
Moreno, RD ;
Schatten, G ;
Ramalho-Santos, J .
BIOLOGY OF REPRODUCTION, 2002, 66 (05) :1259-1266
[64]   POOR OOCYTE QUALITY RATHER THAN IMPLANTATION FAILURE AS A CAUSE OF AGE-RELATED DECLINE IN FEMALE FERTILITY [J].
NAVOT, D ;
BERGH, PA ;
WILLIAMS, MA ;
GARRISI, GJ ;
GUZMAN, I ;
SANDLER, B ;
GRUNFELD, L .
LANCET, 1991, 337 (8754) :1375-1377
[65]   INVOLVEMENT OF SUPEROXIDE RADICALS IN THE MOUSE 2-CELL BLOCK [J].
NODA, Y ;
MATSUMOTO, H ;
UMAOKA, Y ;
TATSUMI, K ;
KISHI, J ;
MORI, T .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1991, 28 (04) :356-360
[66]   The Polycomb-group gene Ezh2 is required for early mouse development [J].
O'Carroll, D ;
Erhardt, S ;
Pagani, M ;
Barton, SC ;
Surani, MA ;
Jenuwein, T .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (13) :4330-4336
[67]   Bmi1, stem cells, and senescence regulation [J].
Park, IK ;
Morrison, SJ ;
Clarke, MF .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (02) :175-179
[68]   Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair [J].
Prolla, TA ;
Baker, SM ;
Harris, AC ;
Tsao, EL ;
Yao, X ;
Bronner, CE ;
Zheng, BH ;
Gordon, M ;
Reneker, J ;
Arnheim, N ;
Shibata, D ;
Bradley, A ;
Liskay, RM .
NATURE GENETICS, 1998, 18 (03) :276-279
[69]   Stemness: Transcriptional profiling of embryonic and adult stem cells [J].
Ramalho-Santos, M ;
Yoon, S ;
Matsuzaki, Y ;
Mulligan, RC ;
Melton, DA .
SCIENCE, 2002, 298 (5593) :597-600
[70]  
Rankin T, 1996, DEVELOPMENT, V122, P2903