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      Genetics of the ovarian reserve

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          Abstract

          Primordial follicles or non-growing follicles (NGFs) are the functional unit of reproduction, each comprising a single germ cell surrounded by supporting somatic cells. NGFs constitute the ovarian reserve (OR), prerequisite for germ cell ovulation and the continuation of the species. The dynamics of the reserve is determined by the number of NGFs formed and their complex subsequent fates. During the reproductive lifespan, the OR progressively diminishes due to follicle atresia as well as recruitment, maturation, and ovulation. The depletion of the OR is the major determining driver of menopause, which ensues when the number of primordial follicles falls below a threshold of ∼1,000. Therefore, genes and processes involved in follicle dynamics are particularly important to understand the process of menopause, both in the typical reproductive lifespan and in conditions like primary ovarian insufficiency, defined as menopause before age 40. Genes and their variants that affect the timing of menopause thereby provide candidates for diagnosis of and intervention in problems of reproductive lifespan. We review the current knowledge of processes and genes involved in the development of the OR and in the dynamics of ovarian follicles.

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          Most cited references232

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          Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4.

          Oct4 is a mammalian POU transcription factor expressed by early embryo cells and germ cells. We report that the activity of Oct4 is essential for the identity of the pluripotential founder cell population in the mammalian embryo. Oct4-deficient embryos develop to the blastocyst stage, but the inner cell mass cells are not pluripotent. Instead, they are restricted to differentiation along the extraembryonic trophoblast lineage. Furthermore, in the absence of a true inner cell mass, trophoblast proliferation is not maintained in Oct4-/- embryos. Expansion of trophoblast precursors is restored, however, by an Oct4 target gene product, fibroblast growth factor-4. Therefore, Oct4 also determines paracrine growth factor signaling from stem cells to the trophectoderm.
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            MIWI2 is essential for spermatogenesis and repression of transposons in the mouse male germline.

            Small RNAs associate with Argonaute proteins and serve as sequence-specific guides for regulation of mRNA stability, productive translation, chromatin organization, and genome structure. In animals, the Argonaute superfamily segregates into two clades. The Argonaute clade acts in RNAi and in microRNA-mediated gene regulation in partnership with 21-22 nt RNAs. The Piwi clade, and their 26-30 nt piRNA partners, have yet to be assigned definitive functions. In mice, two Piwi-family members have been demonstrated to have essential roles in spermatogenesis. Here, we examine the effects of disrupting the gene encoding the third family member, MIWI2. Miwi2-deficient mice display a meiotic-progression defect in early prophase of meiosis I and a marked and progressive loss of germ cells with age. These phenotypes may be linked to an inappropriate activation of transposable elements detected in Miwi2 mutants. Our observations suggest a conserved function for Piwi-clade proteins in the control of transposons in the germline.
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              Developmentally regulated piRNA clusters implicate MILI in transposon control.

              Nearly half of the mammalian genome is composed of repeated sequences. In Drosophila, Piwi proteins exert control over transposons. However, mammalian Piwi proteins, MIWI and MILI, partner with Piwi-interacting RNAs (piRNAs) that are depleted of repeat sequences, which raises questions about a role for mammalian Piwi's in transposon control. A search for murine small RNAs that might program Piwi proteins for transposon suppression revealed developmentally regulated piRNA loci, some of which resemble transposon master control loci of Drosophila. We also find evidence of an adaptive amplification loop in which MILI catalyzes the formation of piRNA 5' ends. Mili mutants derepress LINE-1 (L1) and intracisternal A particle and lose DNA methylation of L1 elements, demonstrating an evolutionarily conserved role for PIWI proteins in transposon suppression.
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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                15 October 2015
                2015
                : 6
                : 308
                Affiliations
                [1] 1Intramural Research Program, National Institute on Aging, National Institutes of Health , Baltimore, MD, USA
                [2] 2Genomic Research Centre, Cante di Montevecchio Association , Fano, Italy
                Author notes

                Edited by: Shin Murakami, Touro University California, USA

                Reviewed by: Gil Atzmon, Albert Einstein College of Medicine, USA; Anatoliy I. Yashin, Duke University, USA; Mark A. McCormick, Buck Institute for Research on Aging, USA

                *Correspondence: Emanuele Pelosi, pelosie@ 123456mail.nih.gov

                This article was submitted to Genetics of Aging, a section of the journal Frontiers in Genetics.

                Article
                10.3389/fgene.2015.00308
                4606124
                26528328
                d4690fb1-286d-40c0-82a6-c94210957365
                Copyright © 2015 Pelosi, Forabosco and Schlessinger.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 July 2015
                : 24 September 2015
                Page count
                Figures: 1, Tables: 0, Equations: 0, References: 271, Pages: 20, Words: 20311
                Categories
                Genetics
                Review

                Genetics
                ovarian reserve,reproduction,reproductive lifespan,menopause,folliculogenesis
                Genetics
                ovarian reserve, reproduction, reproductive lifespan, menopause, folliculogenesis

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