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      Nanos promotes epigenetic reprograming of the germline by down-regulation of the THAP transcription factor LIN-15B

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          Abstract

          Nanos RNA-binding proteins are required for germline development in metazoans, but the underlying mechanisms remain poorly understood. We have profiled the transcriptome of primordial germ cells (PGCs) lacking the nanos homologs nos-1 and nos-2 in C. elegans. nos-1nos-2 PGCs fail to silence hundreds of transcripts normally expressed in oocytes. We find that this misregulation is due to both delayed turnover of maternal transcripts and inappropriate transcriptional activation. The latter appears to be an indirect consequence of delayed turnover of the maternally-inherited transcription factor LIN-15B, a synMuvB class transcription factor known to antagonize PRC2 activity. PRC2 is required for chromatin reprogramming in the germline, and the transcriptome of PGCs lacking PRC2 resembles that of nos-1nos-2 PGCs. Loss of maternal LIN-15B restores fertility to nos-1nos-2 mutants. These findings suggest that Nanos promotes germ cell fate by downregulating maternal RNAs and proteins that would otherwise interfere with PRC2-dependent reprogramming of PGC chromatin.

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          Every new embryo inherits a set of starting instructions from its mother. These instructions are called a ‘maternal dowry’ and help a fertilized egg through the first few stages of development. Later, the maternal dowry is removed so that the embryo’s genetic instructions can take over.

          In animals, some of the cells in this early embryo become specialized to produce eggs (technically called oocytes) or sperm. These cells are called germ cells, and they are needed for reproduction. A protein called Nanos helps germ cells become different to other cells, but it is not clear how Nanos has this effect.

          Lee et al. studied Nanos in the embryos of the worm Caenorhabditis elegans. In many ways, early development is the same in the worm as in many other animals. By examining worms that did not have Nanos, Lee et al. showed that germ cells without Nanos do not lose their maternal dowry. As a result, the cells still contain a molecule called LIN-15B, which makes other types of cells in the worm. Ultimately, without Nanos, the germ cells do not develop and die leaving the worm sterile.

          Germ cells are essential for living things to reproduce and have children. Understanding how they are created can teach scientists a lot about how embryos develop before birth. This could eventually help to boost fertility in endangered species or to treat human sterility.

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          Most cited references62

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          Specific interference by ingested dsRNA.

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            UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development.

            The trithorax and the polycomb group proteins are chromatin modifiers, which play a key role in the epigenetic regulation of development, differentiation and maintenance of cell fates. The polycomb repressive complex 2 (PRC2) mediates transcriptional repression by catalysing the di- and tri-methylation of Lys 27 on histone H3 (H3K27me2/me3). Owing to the essential role of the PRC2 complex in repressing a large number of genes involved in somatic processes, the H3K27me3 mark is associated with the unique epigenetic state of stem cells. The rapid decrease of the H3K27me3 mark during specific stages of embryogenesis and stem-cell differentiation indicates that histone demethylases specific for H3K27me3 may exist. Here we show that the human JmjC-domain-containing proteins UTX and JMJD3 demethylate tri-methylated Lys 27 on histone H3. Furthermore, we demonstrate that ectopic expression of JMJD3 leads to a strong decrease of H3K27me3 levels and causes delocalization of polycomb proteins in vivo. Consistent with the strong decrease in H3K27me3 levels associated with HOX genes during differentiation, we show that UTX directly binds to the HOXB1 locus and is required for its activation. Finally mutation of F18E9.5, a Caenorhabditis elegans JMJD3 orthologue, or inhibition of its expression, results in abnormal gonad development. Taken together, these results suggest that H3K27me3 demethylation regulated by UTX/JMJD3 proteins is essential for proper development. Moreover, the recent demonstration that UTX associates with the H3K4me3 histone methyltransferase MLL2 (ref. 8) supports a model in which the coordinated removal of repressive marks, polycomb group displacement, and deposition of activating marks are important for the stringent regulation of transcription during cellular differentiation.
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              Blimp1 is a critical determinant of the germ cell lineage in mice.

              Germ cell fate in mice is induced in pluripotent epiblast cells in response to signals from extraembryonic tissues. The specification of approximately 40 founder primordial germ cells and their segregation from somatic neighbours are important events in early development. We have proposed that a critical event during this specification includes repression of a somatic programme that is adopted by neighbouring cells. Here we show that Blimp1 (also known as Prdm1), a known transcriptional repressor, has a critical role in the foundation of the mouse germ cell lineage, as its disruption causes a block early in the process of primordial germ cell formation. Blimp1-deficient mutant embryos form a tight cluster of about 20 primordial germ cell-like cells, which fail to show the characteristic migration, proliferation and consistent repression of homeobox genes that normally accompany specification of primordial germ cells. Furthermore, our genetic lineage-tracing experiments indicate that the Blimp1-positive cells originating from the proximal posterior epiblast cells are indeed the lineage-restricted primordial germ cell precursors.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                07 November 2017
                2017
                : 6
                : e30201
                Affiliations
                [1]deptDepartment of Molecular Biology and Genetics Howard Hughes Medical Institute, Johns Hopkins University School of Medicine BaltimoreUnited States
                University of Cambridge United Kingdom
                University of Cambridge United Kingdom
                Author information
                http://orcid.org/0000-0003-0982-2150
                http://orcid.org/0000-0002-5697-300X
                http://orcid.org/0000-0001-8257-0493
                Article
                30201
                10.7554/eLife.30201
                5734877
                29111977
                b023ac31-5bfe-45d5-b967-4d5e9deef679
                © 2017, Lee et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 06 July 2017
                : 06 November 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01HD37047
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000011, Howard Hughes Medical Institute;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100001021, Damon Runyon Cancer Research Foundation;
                Award ID: DRG-2417‐13
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Cell Biology
                Developmental Biology and Stem Cells
                Custom metadata
                Nanos is required for germline specification by erasure of maternal program in primordial germ cells.

                Life sciences
                nanos rna binding protein,c. elegans germline,synmuvb,germ cell fate,primordial germ cells,lin-15b,c. elegans

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