Literature DB >> 29748894

The capacity of oocytes for DNA repair.

Jessica M Stringer1, Amy Winship1, Seng H Liew1, Karla Hutt2.   

Abstract

Female fertility and offspring health are critically dependent on the maintenance of an adequate supply of high-quality oocytes. Like somatic cells, oocytes are subject to a variety of different types of DNA damage arising from endogenous cellular processes and exposure to exogenous genotoxic stressors. While the repair of intentionally induced DNA double strand breaks in gametes during meiotic recombination is well characterised, less is known about the ability of oocytes to repair pathological DNA damage and the relative contribution of DNA repair to oocyte quality is not well defined. This review will discuss emerging data suggesting that oocytes are in fact capable of efficient DNA repair and that DNA repair may be an important mechanism for ensuring female fertility, as well as the transmission of high-quality genetic material to subsequent generations.

Keywords:  Base excision repair; Detection and response; Folliculogenesis; Homologous recombination; Mismatch repair; Non-homologous end joining; Nucleotide excision repair; Ovary; Primordial follicles

Mesh:

Year:  2018        PMID: 29748894     DOI: 10.1007/s00018-018-2833-9

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  184 in total

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Authors:  Deborah E Barnes; Tomas Lindahl
Journal:  Annu Rev Genet       Date:  2004       Impact factor: 16.830

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Authors:  Sheila S David; Valerie L O'Shea; Sucharita Kundu
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Review 7.  Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.

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8.  Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma.

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Journal:  Genes Dev       Date:  1996-10-01       Impact factor: 11.361

9.  Inactivation of the poly(ADP-ribose) polymerase gene affects oxygen radical and nitric oxide toxicity in islet cells.

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Journal:  J Biol Chem       Date:  1995-05-12       Impact factor: 5.157

Review 10.  The DNA damage response and cancer therapy.

Authors:  Christopher J Lord; Alan Ashworth
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  21 in total

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4.  Environmentally relevant exposure to dibutyl phthalate disrupts DNA damage repair gene expression in the mouse ovary†.

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6.  Checkpoint inhibitor immunotherapy diminishes oocyte number and quality in mice.

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Review 9.  Genetic Instability and Chromatin Remodeling in Spermatids.

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Review 10.  Crosstalk between PTEN/PI3K/Akt Signalling and DNA Damage in the Oocyte: Implications for Primordial Follicle Activation, Oocyte Quality and Ageing.

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