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      Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells

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          Abstract

          Although mitochondria are widely studied organelles, the recent interest in the role of mitochondrial small noncoding RNAs (sncRNAs), miRNAs, and more recently, piRNAs, is providing new functional perspectives in germ cell development and differentiation. piRNAs (PIWI-interacting RNAs) are single-stranded sncRNAs of mostly about 20–35 nucleotides, generated from the processing of pre-piRNAs. We leverage next-generation sequencing data obtained from mouse primordial germ cells and somatic cells purified from early-differentiating embryonic ovaries and testis from 11.5 to 13.5 days postcoitum. Using bioinformatic tools, we elucidate (i) the origins of piRNAs as transcribed from mitochondrial DNA fragments inserted in the nucleus or from the mitochondrial genome; (ii) their levels of expression; and (iii) their potential roles, as well as their association with genomic regions encoding other sncRNAs (such as tRNAs and rRNAs) and the mitochondrial regulatory region (D-loop). Finally, our results suggest how nucleo-mitochondrial communication, both anterograde and retrograde signaling, may be mediated by mitochondria-associated piRNAs.

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          miRBase: from microRNA sequences to function

          Abstract miRBase catalogs, names and distributes microRNA gene sequences. The latest release of miRBase (v22) contains microRNA sequences from 271 organisms: 38 589 hairpin precursors and 48 860 mature microRNAs. We describe improvements to the database and website to provide more information about the quality of microRNA gene annotations, and the cellular functions of their products. We have collected 1493 small RNA deep sequencing datasets and mapped a total of 5.5 billion reads to microRNA sequences. The read mapping patterns provide strong support for the validity of between 20% and 65% of microRNA annotations in different well-studied animal genomes, and evidence for the removal of >200 sequences from the database. To improve the availability of microRNA functional information, we are disseminating Gene Ontology terms annotated against miRBase sequences. We have also used a text-mining approach to search for microRNA gene names in the full-text of open access articles. Over 500 000 sentences from 18 542 papers contain microRNA names. We score these sentences for functional information and link them with 12 519 microRNA entries. The sentences themselves, and word clouds built from them, provide effective summaries of the functional information about specific microRNAs. miRBase is publicly and freely available at http://mirbase.org/.
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            Small silencing RNAs: an expanding universe.

            Since the discovery in 1993 of the first small silencing RNA, a dizzying number of small RNA classes have been identified, including microRNAs (miRNAs), small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs). These classes differ in their biogenesis, their modes of target regulation and in the biological pathways they regulate. There is a growing realization that, despite their differences, these distinct small RNA pathways are interconnected, and that small RNA pathways compete and collaborate as they regulate genes and protect the genome from external and internal threats.
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              The multifaceted contributions of mitochondria to cellular metabolism

              Although classically appreciated for their role as the powerhouse of the cell, the metabolic functions of mitochondria reach far beyond bioenergetics. Mitochondria catabolize nutrients for energy, generate biosynthetic precursors for macromolecules, compartmentalize metabolites for the maintenance of redox homeostasis, and function as hubs for metabolic waste management. We discuss the importance of these roles in both normal physiology and in disease.
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                Author and article information

                Contributors
                brienoenriquezma@mwri.magee.edu
                jdelmazo@cib.csic.es
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                24 June 2022
                24 June 2022
                2022
                : 12
                : 10730
                Affiliations
                [1 ]GRID grid.418281.6, ISNI 0000 0004 1794 0752, Department of Cellular and Molecular Biology, , Centro de Investigaciones Biológicas Margarita Salas C.I.B. (CSIC), ; Ramiro de Maeztu 9, 28040 Madrid, Spain
                [2 ]GRID grid.26811.3c, ISNI 0000 0001 0586 4893, Institute of Bioengineering, , University “Miguel Hernández”, ; Elche, Spain
                [3 ]GRID grid.15667.33, ISNI 0000 0004 1757 0843, Department of Experimental Oncology, , IEO European Institute of Oncology–IRCCS, ; Milan, Italy
                [4 ]GRID grid.4708.b, ISNI 0000 0004 1757 2822, Department of Health Sciences, , University of Milan, ; Milan, Italy
                [5 ]GRID grid.21925.3d, ISNI 0000 0004 1936 9000, Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences. School of Medicine, , University of Pittsburgh, ; Pittsburgh, USA
                Article
                14414
                10.1038/s41598-022-14414-4
                9232517
                35750721
                a8212e03-4c47-4467-adf3-36081db1a9fc
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 19 October 2021
                : 18 May 2022
                Funding
                Funded by: Agencia Estatal de Investigación; Ministerio de Ciencia, Innovación y Universidades
                Award ID: BFU2017-87095-R
                Award ID: BFU2017-87095-R
                Award ID: BFU2017-87095-R
                Award ID: BFU2017-87095-R
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100009633, Eunice Kennedy Shriver National Institute of Child Health and Human Development;
                Award ID: R00HD090289
                Award Recipient :
                Funded by: Magee Auxiliary Research Scholar (MARS) endowment
                Categories
                Article
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                © The Author(s) 2022

                Uncategorized
                cell biology,developmental biology
                Uncategorized
                cell biology, developmental biology

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