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      Regulated dicing of pre-mir-144 via reshaping of its terminal loop

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          Abstract

          Although the route to generate microRNAs (miRNAs) is often depicted as a linear series of sequential and constitutive cleavages, we now appreciate multiple alternative pathways as well as diverse strategies to modulate their processing and function. Here, we identify an unusually profound regulatory role of conserved loop sequences in vertebrate pre-mir-144, which are essential for its cleavage by the Dicer RNase III enzyme in human and zebrafish models. Our data indicate that pre-mir-144 dicing is positively regulated via its terminal loop, and involves the ILF3 complex (NF90 and its partner NF45/ILF2). We provide further evidence that this regulatory switch involves reshaping of the pre-mir-144 apical loop into a structure that is appropriate for Dicer cleavage. In light of our recent findings that mir-144 promotes the nuclear biogenesis of its neighbor mir-451, these data extend the complex hierarchy of nuclear and cytoplasmic regulatory events that can control the maturation of clustered miRNAs.

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          Metazoan MicroRNAs

          MicroRNAs (miRNAs) are ∼22 nt RNAs that direct posttranscriptional repression of mRNA targets in diverse eukaryotic lineages. In humans and other mammals, these small RNAs help sculpt the expression of most mRNAs. This article reviews advances in our understanding of the defining features of metazoan miRNAs and their biogenesis, genomics, and evolution. It then reviews how metazoan miRNAs are regulated, how they recognize and cause repression of their targets, and the biological functions of this repression, with a compilation of knockout phenotypes that shows that important biological functions have been identified for most of the broadly conserved miRNAs of mammals.
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            Regulation of microRNA biogenesis and its crosstalk with other cellular pathways

            MicroRNAs (miRNAs) are short non-coding RNAs that inhibit the expression of target genes by directly binding to their mRNAs. miRNAs are transcribed as precursor molecules, which are subsequently cleaved by the endoribonucleases Drosha and Dicer. Mature miRNAs are bound by a member of the Argonaute (AGO) protein family to form the RNA-induced silencing complex (RISC) in a process termed RISC loading. Advances in structural analyses of Drosha and Dicer complexes enabled elucidation of the mechanisms that drive these molecular machines. Transcription of miRNAs, their processing by Drosha and Dicer and RISC loading are key steps in miRNA biogenesis, and various additional factors facilitate, support or inhibit these processes. Recent work has revealed that regulatory factors not only coordinate individual miRNA processing steps but also connect miRNA biogenesis with other cellular processes. Protein phosphorylation, for example, links miRNA biogenesis to various signalling pathways, and such modifications are often associated with disease. Furthermore, not all miRNAs follow canonical processing routes, and many non-canonical miRNA biogenesis pathways have recently been characterized.
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              A large-scale binding and functional map of human RNA-binding proteins

              Many proteins regulate the expression of genes by binding to specific regions encoded in the genome 1 . Here we introduce a new data set of RNA elements in the human genome that are recognized by RNA-binding proteins (RBPs), generated as part of the Encyclopedia of DNA Elements (ENCODE) project phase III. This class of regulatory elements functions only when transcribed into RNA, as they serve as the binding sites for RBPs that control post-transcriptional processes such as splicing, cleavage and polyadenylation, and the editing, localization, stability and translation of mRNAs. We describe the mapping and characterization of RNA elements recognized by a large collection of human RBPs in K562 and HepG2 cells. Integrative analyses using five assays identify RBP binding sites on RNA and chromatin in vivo, the in vitro binding preferences of RBPs, the function of RBP binding sites and the subcellular localization of RBPs, producing 1,223 replicated data sets for 356 RBPs. We describe the spectrum of RBP binding throughout the transcriptome and the connections between these interactions and various aspects of RNA biology, including RNA stability, splicing regulation and RNA localization. These data expand the catalogue of functional elements encoded in the human genome by the addition of a large set of elements that function at the RNA level by interacting with RBPs.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                22 July 2022
                08 July 2022
                08 July 2022
                : 50
                : 13
                : 7637-7654
                Affiliations
                Developmental Biology Program, Sloan Kettering Institute , 1275 York Ave, Box 252, New York, NY 10065, USA
                Department of Biochemistry, Boston University School of Medicine , Boston, MA 02118, USA
                The Jackson Laboratory for Genomic Medicine , Farmington, CT 06032, USA
                Regensburg Center for Biochemistry (RCB), Laboratory for RNA Biology, University of Regensburg , 93053 Regensburg, Germany
                Regensburg Center for Biochemistry (RCB), Laboratory for RNA Biology, University of Regensburg , 93053 Regensburg, Germany
                Developmental Biology Program, Sloan Kettering Institute , 1275 York Ave, Box 252, New York, NY 10065, USA
                The Jackson Laboratory for Genomic Medicine , Farmington, CT 06032, USA
                Regensburg Center for Biochemistry (RCB), Laboratory for RNA Biology, University of Regensburg , 93053 Regensburg, Germany
                Department of Biochemistry, Boston University School of Medicine , Boston, MA 02118, USA
                Developmental Biology Program, Sloan Kettering Institute , 1275 York Ave, Box 252, New York, NY 10065, USA
                Author notes
                To whom correspondence should be addressed. Tel: +1 212 639 5578; Fax: +1 212 717 3604; Email: laie@ 123456mskcc.org
                Author information
                https://orcid.org/0000-0002-8432-5851
                Article
                gkac568
                10.1093/nar/gkac568
                9303283
                35801921
                7a618459-0cec-42d7-b751-28089cf765ca
                © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 June 2022
                : 10 June 2022
                : 09 February 2022
                Page count
                Pages: 18
                Funding
                Funded by: NIH, DOI 10.13039/100000002;
                Award ID: R01GM130935-03
                Award ID: R01-NS094637
                Award ID: R01-GM083300
                Award ID: R01-HL135564
                Funded by: Susan and Peter Solomon Divisional Genomics Program;
                Funded by: M.S.K. Core;
                Award ID: P30-CA008748
                Categories
                AcademicSubjects/SCI00010
                RNA and RNA-protein complexes

                Genetics
                Genetics

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