Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000072.xml
Semin Reprod Med 2015; 33(06): 384-388
DOI: 10.1055/s-0035-1567824
DOI: 10.1055/s-0035-1567824
Impaired DNA Repair as a Mechanism for Oocyte Aging: Is It Epigenetically Determined?
Further Information
Publication History
Publication Date:
12 November 2015 (online)
Abstract
DNA damage is one of the most common insults that challenge all cells, and more so in resting cell-like oocytes. Increased DNA damage in aged oocyte has been shown to negatively impact the reproductive outcomes. The underlying molecular mechanism is still not completely comprehended, but based on the literature, this decline in the aging oocyte is attributed to impaired DNA repair and epigenetic modifications of these genes with increasing age. In this review, we discuss these molecular alterations and the epigenetic modifications in the DNA double strand break repair gene expressions as a mechanism of oocyte aging.
-
References
- 1 Tosato M, Zamboni V, Ferrini A, Cesari M. The aging process and potential interventions to extend life expectancy. Clin Interv Aging 2007; 2 (3) 401-412
- 2 Agarwal A, Gupta S, Sharma RK. Role of oxidative stress in female reproduction. Reprod Biol Endocrinol 2005; 3: 28
- 3 Kimberly L, Case A, Cheung AP , et al. Advanced reproductive age and fertility: no. 269, November 2011. Int J Gynaecol Obstet 2012; 117 (1) 95-102
- 4 Liu L, Keefe DL. Ageing-associated aberration in meiosis of oocytes from senescence-accelerated mice. Hum Reprod 2002; 17 (10) 2678-2685
- 5 Hasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J. Aging and genome maintenance: lessons from the mouse?. Science 2003; 299 (5611) 1355-1359
- 6 Ehrlich S. Effect of fertility and infertility on longevity. Fertil Steril 2015; 103 (5) 1129-1135
- 7 Rocca WA, van Duijn CM, Clayton D , et al; EURODEM Risk Factors Research Group. Maternal age and Alzheimer's disease: a collaborative re-analysis of case-control studies. Int J Epidemiol 1991; 20 (Suppl. 02) S21-S27
- 8 Kemkes-Grottenthaler A. Parental effects on offspring longevity—evidence from 17th to 19th century reproductive histories. Ann Hum Biol 2004; 31 (2) 139-158
- 9 Brion MJ, Leary SD, Lawlor DA, Smith GD, Ness AR. Modifiable maternal exposures and offspring blood pressure: a review of epidemiological studies of maternal age, diet, and smoking. Pediatr Res 2008; 63 (6) 593-598
- 10 Gale EA. Maternal age and diabetes in childhood. BMJ 2010; 340: c623
- 11 Livera G, Petre-Lazar B, Guerquin MJ, Trautmann E, Coffigny H, Habert R. p63 null mutation protects mouse oocytes from radio-induced apoptosis. Reproduction 2008; 135 (1) 3-12
- 12 Carroll J, Marangos P. The DNA damage response in mammalian oocytes. Front Genet 2013; 4: 117
- 13 Derijck A, van der Heijden G, Giele M, Philippens M, de Boer P. DNA double-strand break repair in parental chromatin of mouse zygotes, the first cell cycle as an origin of de novo mutation. Hum Mol Genet 2008; 17 (13) 1922-1937
- 14 Chiang HC, Elledge R, Larson P, Jatoi I, Li R, Hu Y. Effects of radiation therapy on breast epithelial cells in BRCA1/2 mutation carriers. Breast Cancer (Auckl) 2015; 9: 25-29
- 15 Gudmundsdottir K, Ashworth A. The roles of BRCA1 and BRCA2 and associated proteins in the maintenance of genomic stability. Oncogene 2006; 25 (43) 5864-5874
- 16 Xiong B, Li S, Ai JS , et al. BRCA1 is required for meiotic spindle assembly and spindle assembly checkpoint activation in mouse oocytes. Biol Reprod 2008; 79 (4) 718-726
- 17 Tirkkonen M, Johannsson O, Agnarsson BA , et al. Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res 1997; 57 (7) 1222-1227
- 18 Wang Q, Zhang H, Fishel R, Greene MI. BRCA1 and cell signaling. Oncogene 2000; 19 (53) 6152-6158
- 19 Soleimani R, Heytens E, Oktay K. Enhancement of neoangiogenesis and follicle survival by sphingosine-1-phosphate in human ovarian tissue xenotransplants. PLoS ONE 2011; 6 (4) e19475
- 20 Titus S, Li F, Stobezki R , et al. Impairment of BRCA1-related DNA double-strand break repair leads to ovarian aging in mice and humans. Sci Transl Med 2013; 5 (172) 172ra21
- 21 Govindaraj V, Keralapura Basavaraju R, Rao AJ. Changes in the expression of DNA double strand break repair genes in primordial follicles from immature and aged rats. Reprod Biomed Online 2015; 30 (3) 303-310
- 22 Huber LJ, Yang TW, Sarkisian CJ, Master SR, Deng CX, Chodosh LA. Impaired DNA damage response in cells expressing an exon 11-deleted murine Brca1 variant that localizes to nuclear foci. Mol Cell Biol 2001; 21 (12) 4005-4015
- 23 Zhang D, Zhang X, Zeng M , et al. Increased DNA damage and repair deficiency in granulosa cells are associated with ovarian aging in rhesus monkey. J Assist Reprod Genet 2015; 32 (7) 1069-1078
- 24 Oktay K, Turan V, Titus S, Stobezki R, Liu L. BRCA mutations, DNA repair deficiency and ovarian aging. Biol Reprod 2015;
- 25 Oktay K, Moy F, Titus S , et al. Age-related decline in DNA repair function explains diminished ovarian reserve, earlier menopause, and possible oocyte vulnerability to chemotherapy in women with BRCA mutations. J Clin Oncol 2014; 32 (10) 1093-1094
- 26 Goldberg AD, Allis CD, Bernstein E. Epigenetics: a landscape takes shape. Cell 2007; 128 (4) 635-638
- 27 Wilson VL, Jones PA. DNA methylation decreases in aging but not in immortal cells. Science 1983; 220 (4601) 1055-1057
- 28 Lu T, Pan Y, Kao SY , et al. Gene regulation and DNA damage in the ageing human brain. Nature 2004; 429 (6994) 883-891
- 29 Bird A. DNA methylation patterns and epigenetic memory. Genes Dev 2002; 16 (1) 6-21
- 30 Hannum G, Guinney J, Zhao L , et al. Genome-wide methylation profiles reveal quantitative views of human aging rates. Mol Cell 2013; 49 (2) 359-367
- 31 Liu L, Wylie RC, Andrews LG, Tollefsbol TO. Aging, cancer and nutrition: the DNA methylation connection. Mech Ageing Dev 2003; 124 (10–12) 989-998
- 32 Yue MX, Fu XW, Zhou GB , et al. Abnormal DNA methylation in oocytes could be associated with a decrease in reproductive potential in old mice. J Assist Reprod Genet 2012; 29 (7) 643-650
- 33 Qian Y, Tu J, Tang NL , et al. Dynamic changes of DNA epigenetic marks in mouse oocytes during natural and accelerated aging. Int J Biochem Cell Biol 2015; 67: 121-127
- 34 De La Fuente R, Baumann C, Viveiros MM. Chromatin structure and ATRX function in mouse oocytes. Results Probl Cell Differ 2012; 55: 45-68
- 35 Guglielmino MR, Santonocito M, Vento M , et al. TAp73 is downregulated in oocytes from women of advanced reproductive age. Cell Cycle 2011; 10 (19) 3253-3256
- 36 Jones PA, Baylin SB. The fundamental role of epigenetic events in cancer. Nat Rev Genet 2002; 3 (6) 415-428
- 37 Kim WJ, Vo QN, Shrivastav M, Lataxes TA, Brown KD. Aberrant methylation of the ATM promoter correlates with increased radiosensitivity in a human colorectal tumor cell line. Oncogene 2002; 21 (24) 3864-3871
- 38 Goodarzi AA, Noon AT, Deckbar D , et al. ATM signaling facilitates repair of DNA double-strand breaks associated with heterochromatin. Mol Cell 2008; 31 (2) 167-177
- 39 Meglicki M, Zientarski M, Borsuk E. Constitutive heterochromatin during mouse oogenesis: the pattern of histone H3 modifications and localization of HP1alpha and HP1beta proteins. Mol Reprod Dev 2008; 75 (2) 414-428
- 40 Manosalva I, González A. Aging alters histone H4 acetylation and CDC2A in mouse germinal vesicle stage oocytes. Biol Reprod 2009; 81 (6) 1164-1171
- 41 van den Berg IM, Eleveld C, van der Hoeven M , et al. Defective deacetylation of histone 4 K12 in human oocytes is associated with advanced maternal age and chromosome misalignment. Hum Reprod 2011; 26 (5) 1181-1190
- 42 Van Blerkom J. Mitochondria in human oogenesis and preimplantation embryogenesis: engines of metabolism, ionic regulation and developmental competence. Reproduction 2004; 128 (3) 269-280
- 43 Amicarelli F, Ragnelli AM, Aimola P , et al. Age-dependent ultrastructural alterations and biochemical response of rat skeletal muscle after hypoxic or hyperoxic treatments. Biochim Biophys Acta 1999; 1453 (1) 105-114
- 44 Tatone C, Carbone MC, Falone S , et al. Age-dependent changes in the expression of superoxide dismutases and catalase are associated with ultrastructural modifications in human granulosa cells. Mol Hum Reprod 2006; 12 (11) 655-660
- 45 Lu Y, Chu A, Turker MS, Glazer PM. Hypoxia-induced epigenetic regulation and silencing of the BRCA1 promoter. Mol Cell Biol 2011; 31 (16) 3339-3350