Age-Specific Gene Expression Profiles of Rhesus Monkey Ovaries Detected by Microarray Analysis
文献类型: 外文期刊
作者: Wei, Hengxi 1 ; Liu, Xiangjie 1 ; Yuan, Jihong 2 ; Li, Li 1 ; Zhang, Dongdong 3 ; Guo, Xinzheng 1 ; Liu, Lin; Zhang, S 1 ;
作者机构: 1.South China Agr Univ, Guangdong Prov Key Lab Agroanim Genom & Mol Breed, Natl Engn Res Ctr Breeding Swine Ind, Coll Anim Sci, Guangzhou 510642, Guangdong, Peoples R China
2.Nankai Univ, Dept Cell Biol & Genet, Coll Life Sci, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
3.Nankai Univ, Dept Cell Biol & Genet, Coll Life Sci
期刊名称:BIOMED RESEARCH INTERNATIONAL ( 影响因子:3.411; 五年影响因子:3.62 )
ISSN: 2314-6133
年卷期: 2015 年
页码:
收录情况: SCI
摘要: The biological function of human ovaries declines with age. To identify the potential molecular changes in ovarian aging, we performed genome-wide gene expression analysis by microarray of ovaries from young, middle-aged, and old rhesus monkeys. Microarray data was validated by quantitative real-time PCR. Results showed that a total of 503 (60 upregulated, 443 downregulated) and 84 (downregulated) genes were differentially expressed in old ovaries compared to young and middle-aged groups, respectively. No difference in gene expression was found between middle-aged and young groups. Differentially expressed genes were mainly enriched in cell and organelle, cellular and physiological process, binding, and catalytic activity. These genes were primarily associated with KEGG pathways of cell cycle, DNA replication and repair, oocyte meiosis and maturation, MAPK, TGF-beta, and p53 signaling pathway. Genes upregulated were involved in aging, defense response, oxidation reduction, and negative regulation of cellular process; genes downregulated have functions in reproduction, cell cycle, DNA and RNA process, macromolecular complex assembly, and positive regulation of macromolecule metabolic process. These findings show that monkey ovary undergoes substantial change in global transcription with age. Gene expression profiles are useful in understanding the mechanisms underlying ovarian aging and age-associated infertility in primates.
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