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      RNA: The Unsuspected Conductor in the Orchestra of Macromolecular Crowding

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          Abstract

          This comprehensive Review delves into the chemical principles governing RNA-mediated crowding events, commonly referred to as granules or biological condensates. We explore the pivotal role played by RNA sequence, structure, and chemical modifications in these processes, uncovering their correlation with crowding phenomena under physiological conditions. Additionally, we investigate instances where crowding deviates from its intended function, leading to pathological consequences. By deepening our understanding of the delicate balance that governs molecular crowding driven by RNA and its implications for cellular homeostasis, we aim to shed light on this intriguing area of research. Our exploration extends to the methodologies employed to decipher the composition and structural intricacies of RNA granules, offering a comprehensive overview of the techniques used to characterize them, including relevant computational approaches. Through two detailed examples highlighting the significance of noncoding RNAs, NEAT1 and XIST, in the formation of phase-separated assemblies and their influence on the cellular landscape, we emphasize their crucial role in cellular organization and function. By elucidating the chemical underpinnings of RNA-mediated molecular crowding, investigating the role of modifications, structures, and composition of RNA granules, and exploring both physiological and aberrant phase separation phenomena, this Review provides a multifaceted understanding of the intriguing world of RNA-mediated biological condensates.

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            Biomolecular condensates: organizers of cellular biochemistry

            In addition to membrane-bound organelles, eukaryotic cells feature various membraneless compartments, including the centrosome, the nucleolus and various granules. Many of these compartments form through liquid–liquid phase separation, and the principles, mechanisms and regulation of their assembly as well as their cellular functions are now beginning to emerge.
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              Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq.

              An extensive repertoire of modifications is known to underlie the versatile coding, structural and catalytic functions of RNA, but it remains largely uncharted territory. Although biochemical studies indicate that N(6)-methyladenosine (m(6)A) is the most prevalent internal modification in messenger RNA, an in-depth study of its distribution and functions has been impeded by a lack of robust analytical methods. Here we present the human and mouse m(6)A modification landscape in a transcriptome-wide manner, using a novel approach, m(6)A-seq, based on antibody-mediated capture and massively parallel sequencing. We identify over 12,000 m(6)A sites characterized by a typical consensus in the transcripts of more than 7,000 human genes. Sites preferentially appear in two distinct landmarks--around stop codons and within long internal exons--and are highly conserved between human and mouse. Although most sites are well preserved across normal and cancerous tissues and in response to various stimuli, a subset of stimulus-dependent, dynamically modulated sites is identified. Silencing the m(6)A methyltransferase significantly affects gene expression and alternative splicing patterns, resulting in modulation of the p53 (also known as TP53) signalling pathway and apoptosis. Our findings therefore suggest that RNA decoration by m(6)A has a fundamental role in regulation of gene expression.
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                Author and article information

                Journal
                Chem Rev
                Chem Rev
                cr
                chreay
                Chemical Reviews
                American Chemical Society
                0009-2665
                1520-6890
                05 April 2024
                24 April 2024
                : 124
                : 8
                : 4734-4777
                Affiliations
                []RNA Systems Biology Lab, Center for Human Technologies, Istituto Italiano di Tecnologia , Via Enrico Melen, 83, 16152 Genova, Italy
                []RNA Biology Laboratory, Faculty of Pharmaceutical Sciences, Hokkaido University , Sapporo 060-0812, Japan
                [§ ]Central RNA Lab, Center for Human Technologies, Istituto Italiano di Tecnologia , Via Enrico Melen, 83, 16152 Genova, Italy
                []UK Dementia Research Institute at the Maurice Wohl Institute of King’s College London , London SE5 9RT, U.K.
                []Department of Biological Chemistry, David Geffen School of Medicine at the University of California Los Angeles , Los Angeles, California 90095, United States
                [# ]Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London , London E1 4NS, U.K.
                []Unit of Cell and developmental Biology, Department of Biology, Università di Pisa , 56123 Pisa, Italy
                []Unitat de Bioquímica, Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona , 08193 Barcelona, Spain
                []Catalan Institution for Research and Advanced Studies, ICREA , Passeig Lluís Companys 23, 08010 Barcelona, Spain
                Author notes
                Author information
                https://orcid.org/0000-0002-3047-654X
                https://orcid.org/0000-0001-7524-6310
                Article
                10.1021/acs.chemrev.3c00575
                11046439
                38579177
                7224b064-a6f8-48d0-b805-c0e1f1aeb35b
                © 2024 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 14 August 2023
                : 18 January 2024
                : 12 January 2024
                Funding
                Funded by: Orphan Disease Center, Perelman School of Medicine, University of Pennsylvania, doi 10.13039/100018232;
                Award ID: NA
                Funded by: National Institute of Child Health and Human Development, doi 10.13039/100000071;
                Award ID: R01HD098387
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: PID2020-117454RA-I00
                Funded by: FP7 Ideas: European Research Council, doi 10.13039/100011199;
                Award ID: 309545
                Funded by: Rett Syndrome Research Trust, doi 10.13039/100016499;
                Award ID: NA
                Funded by: H2020 Health, doi 10.13039/100010677;
                Award ID: 727658
                Funded by: David Geffen School of Medicine, University of California, Los Angeles, doi 10.13039/100011075;
                Award ID: NA
                Funded by: H2020 Marie Sklodowska-Curie Actions, doi 10.13039/100010665;
                Award ID: 754490
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: RYC2019-026752-I
                Funded by: Università di Pisa, doi 10.13039/501100007514;
                Award ID: NA
                Funded by: H2020 Marie Sklodowska-Curie Actions, doi 10.13039/100010665;
                Award ID: 101063903
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 855923
                Funded by: Horizon 2020 Framework Programme, doi 10.13039/100010661;
                Award ID: 825080
                Funded by: Horizon 2020 Framework Programme, doi 10.13039/100010661;
                Award ID: 101098989
                Funded by: Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California Los Angeles, doi 10.13039/100008623;
                Award ID: NA
                Funded by: Jonsson Comprehensive Cancer Center, doi 10.13039/100007186;
                Award ID: NA
                Funded by: University of California, Los Angeles, doi 10.13039/100007185;
                Award ID: NA
                Funded by: European Molecular Biology Organization, doi 10.13039/100004410;
                Award ID: ALTF 1149-2021
                Categories
                Review
                Custom metadata
                cr3c00575
                cr3c00575

                Chemistry
                Chemistry

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