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      GASZ Is Essential for Male Meiosis and Suppression of Retrotransposon Expression in the Male Germline

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          Abstract

          Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent as Drosophila, Xenopus, and Homo sapiens. Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by the PIWI family (i.e., MILI, MIWI2, and MIWI). MILI is prominent in embryonic and early post-natal germ cells in nuage also called germinal granules that are often associated with mitochondria and called intermitochondrial cement. We find that GASZ (Germ cell protein with Ankyrin repeats, Sterile alpha motif, and leucine Zipper) co-localizes with MILI in intermitochondrial cement. Knockout of Gasz in mice results in a dramatic downregulation of MILI, and phenocopies the zygotene–pachytene spermatocyte block and male sterility defect observed in MILI null mice. In Gasz null testes, we observe increased hypomethylation and expression of retrotransposons similar to MILI null testes. We also find global shifts in the small RNAome, including down-regulation of repeat-associated, known, and novel piRNAs. These studies provide the first evidence for an essential structural role for GASZ in male fertility and epigenetic and post-transcriptional silencing of retrotransposons by stabilizing MILI in nuage.

          Author Summary

          Many aspects of RNA processing are essential for or prominent in the differentiation of germ cells. Some RNA metabolism in animal germ cells is associated with physical structures surrounding the cell nucleus called nuage. Nuage has a distinct granular appearance prior to the meiotic divisions with unclear functions. We have identified a protein called GASZ, which plays a structural role in this early nuage. In mice lacking GASZ, retrotransposons—endogenous viral-like particles—become released from their typical repressed state in the germline by the loss of small RNAs called piRNAs, resulting in DNA damage and delayed germ cell maturation. Protection of the germline from genetic intruders may require the association of piRNA-synthesizing enzymes and other components of this nuage structure through direct or indirect associations with GASZ. Mutations in GASZ and other nuage components may contribute to infertility in men who do not produce spermatozoa.

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          A distinct small RNA pathway silences selfish genetic elements in the germline.

          In the Drosophila germline, repeat-associated small interfering RNAs (rasiRNAs) ensure genomic stability by silencing endogenous selfish genetic elements such as retrotransposons and repetitive sequences. Whereas small interfering RNAs (siRNAs) derive from both the sense and antisense strands of their double-stranded RNA precursors, rasiRNAs arise mainly from the antisense strand. rasiRNA production appears not to require Dicer-1, which makes microRNAs (miRNAs), or Dicer-2, which makes siRNAs, and rasiRNAs lack the 2',3' hydroxy termini characteristic of animal siRNA and miRNA. Unlike siRNAs and miRNAs, rasiRNAs function through the Piwi, rather than the Ago, Argonaute protein subfamily. Our data suggest that rasiRNAs protect the fly germline through a silencing mechanism distinct from both the miRNA and RNA interference pathways.
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            Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting.

            Imprinted genes are epigenetically marked during gametogenesis so that they are exclusively expressed from either the paternal or the maternal allele in offspring. Imprinting prevents parthenogenesis in mammals and is often disrupted in congenital malformation syndromes, tumours and cloned animals. Although de novo DNA methyltransferases of the Dnmt3 family are implicated in maternal imprinting, the lethality of Dnmt3a and Dnmt3b knockout mice has precluded further studies. We here report the disruption of Dnmt3a and Dnmt3b in germ cells, with their preservation in somatic cells, by conditional knockout technology. Offspring from Dnmt3a conditional mutant females die in utero and lack methylation and allele-specific expression at all maternally imprinted loci examined. Dnmt3a conditional mutant males show impaired spermatogenesis and lack methylation at two of three paternally imprinted loci examined in spermatogonia. By contrast, Dnmt3b conditional mutants and their offspring show no apparent phenotype. The phenotype of Dnmt3a conditional mutants is indistinguishable from that of Dnmt3L knockout mice, except for the discrepancy in methylation at one locus. These results indicate that both Dnmt3a and Dnmt3L are required for methylation of most imprinted loci in germ cells, but also suggest the involvement of other factors.
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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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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                September 2009
                September 2009
                4 September 2009
                : 5
                : 9
                : e1000635
                Affiliations
                [1 ]Department of Pathology, Baylor College of Medicine, Houston, Texas, United States of America
                [2 ]Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, United States of America
                [3 ]Department of Pathology, The Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America
                [4 ]Department of Biology and Biochemistry, University of Houston, Houston, Texas, United States of America
                [5 ]Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America
                [6 ]Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America
                [7 ]Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, Nevada, United States of America
                University of California San Francisco, United States of America
                Author notes

                Conceived and designed the experiments: LM GMB MPG AR KHB WY MMM. Performed the experiments: LM GMB MPG AR KHB DYH WY. Analyzed the data: GMB HZ RAH CC PHG. Contributed reagents/materials/analysis tools: LM GMB KHB HZ RAH CC PHG. Wrote the paper: GMB MMM.

                ¶ These authors also contributed equally to the work.

                Article
                09-PLGE-RA-0465R2
                10.1371/journal.pgen.1000635
                2727916
                19730684
                591c89be-0b2a-4103-9384-fc6136ee10ff
                Ma et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 23 March 2009
                : 6 August 2009
                Page count
                Pages: 15
                Categories
                Research Article
                Cell Biology/Developmental Molecular Mechanisms
                Developmental Biology/Developmental Molecular Mechanisms
                Developmental Biology/Germ Cells
                Genetics and Genomics/Animal Genetics
                Genetics and Genomics/Epigenetics
                Molecular Biology/RNA-Protein Interactions

                Genetics
                Genetics

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