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      Skill Learning Modulates RNA Pol II Poising at Immediate Early Genes in the Adult Striatum

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          Abstract

          A multilayered complexity of epigenetic and transcriptional regulatory mechanisms underlies neuronal activity-dependent gene transcription. The regulation of RNA Pol II progression along the transcription cycle, from promoter-proximal poising (with RNA Pol II paused at promoter-proximal regions, characterized by a Ser5P +-rich and Ser2P +-poor RPB1 CTD) to active elongation, has emerged as a major step in transcriptional regulation across several organisms, tissues, and developmental stages, including the nervous system. However, it is not known whether this mechanism is modulated by experience. We investigated the impact of learning a motor skill on RNA Pol II phosphorylation dynamics in the adult mouse striatum. We uncovered that learning modulates the in vivo striatal phosphorylation dynamics of the CTD of the RNA Pol II RPB1 subunit, leading to an increased poising index in trained mice. We found that this modulation occurs at immediate early genes (IEGs), with increased poising of RNA Pol II at both Arc and Fos genes but not at constitutively expressed genes. Furthermore, we confirmed that this was learning dependent, and not just regulated by context or motor activity. These experiments demonstrate a novel phenomenon of learning induced transcriptional modulation in adult brain, which may have implications for our understanding of learning, memory allocation, and consolidation.

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          Most cited references31

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          Promoter-proximal pausing of RNA polymerase II: emerging roles in metazoans.

          Recent years have witnessed a sea change in our understanding of transcription regulation: whereas traditional models focused solely on the events that brought RNA polymerase II (Pol II) to a gene promoter to initiate RNA synthesis, emerging evidence points to the pausing of Pol II during early elongation as a widespread regulatory mechanism in higher eukaryotes. Current data indicate that pausing is particularly enriched at genes in signal-responsive pathways. Here the evidence for pausing of Pol II from recent high-throughput studies will be discussed, as well as the potential interconnected functions of promoter-proximally paused Pol II.
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            Getting up to speed with transcription elongation by RNA polymerase II.

            Recent advances in sequencing techniques that measure nascent transcripts and that reveal the positioning of RNA polymerase II (Pol II) have shown that the pausing of Pol II in promoter-proximal regions and its release to initiate a phase of productive elongation are key steps in transcription regulation. Moreover, after the release of Pol II from the promoter-proximal region, elongation rates are highly dynamic throughout the transcription of a gene, and vary on a gene-by-gene basis. Interestingly, Pol II elongation rates affect co-transcriptional processes such as splicing, termination and genome stability. Increasing numbers of factors and regulatory mechanisms have been associated with the steps of transcription elongation by Pol II, revealing that elongation is a highly complex process. Elongation is thus now recognized as a key phase in the regulation of transcription by Pol II.
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              Controlling the elongation phase of transcription with P-TEFb.

              The positive transcription elongation factor b (P-TEFb) is a cyclin-dependent kinase that controls the elongation phase of transcription by RNA polymerase II (RNAPII). This process is made possible by the reversal of effects of negative elongation factors that include NELF and DSIF. In complex organisms, elongation control is critical for the regulated expression of most genes. In those organisms, the function of P-TEFb is influenced negatively by HEXIM proteins and 7SK snRNA and positively by a variety of recruiting factors. Phylogenetic analyses of the components of the human elongation control machinery indicate that the number of mechanisms utilized to regulate P-TEFb function increased as organisms developed more complex developmental patterns.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                6 April 2017
                17 April 2017
                Mar-Apr 2017
                : 4
                : 2
                : ENEURO.0074-17.2017
                Affiliations
                [1 ]Champalimaud Neuroscience Programme, Fundação Champalimaud , Lisbon, 1400-038 Portugal
                [2 ]Instituto de Neurociencias, Universidad Miguel Hernández - Consejo Superior de Investigaciones Científicas , Alicante, 03550 Spain
                Author notes

                The authors declare no competing financial interests.

                Author contributions: P.G.-F., M.L., A.B., and R.M.C. designed research; P.G.-F. and M.L. performed research; P.G.-F., M.L., and F.S. analyzed data; P.G.-F. and R.M.C. wrote the paper.

                This work was supported by an FCT fellowship (P.G.-F.) and a Santiago Grisolia fellowship from Generalitat Valenciana (M.L.); by Grants SAF2014-56197-R, PCIN-2015-192-C02-01, and SEV-2013-0317 from the Spanish Ministry of Economy and Competitivity (MINECO) co-financed by the European Regional Development Fund (ERDF); by a NARSAD Independent Investigator Grant from the Brain & Behavior Research Foundation; by a grant from the Alicia Koplowitz Foundation (A.B.) (The Instituto de Neurociencias, a Centre of Excellence Severo Ochoa); and by ERA-NET (F4T), ERC (COG 617142) and HHMI (IEC 55007415) (to R.M.C.). The Instituto de Neurociencias, a Centre of Excellence “Severo Ochoa”.

                Correspondence should be addressed to Rui M. Costa at the above address, E-mail: rui.costa@ 123456neuro.fchampalimaud.org .
                Author information
                http://orcid.org/0000-0002-6288-8426
                Article
                eN-NWR-0074-17
                10.1523/ENEURO.0074-17.2017
                5392706
                4875b339-62ca-486e-aa6c-6a7ae8b45a9d
                Copyright © 2017 Galvão-Ferreira et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 7 March 2017
                : 10 March 2017
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 33, Pages: 12, Words: 8884
                Funding
                Funded by: Ministerio de Economía y Competitividad (MINECO)
                Award ID: 501100003329
                Award ID: SAF2014-56197-R
                Award ID: PCIN-2015-192-C02-01 and SEV-2013-0317
                Funded by: Brain and Behavior Research Foundation (Brain & Behavior Research Foundation)
                Award ID: 100000874
                Funded by: Fundación Alicia Koplowitz (Alicia Koplowitz Foundation)
                Award ID: 100008062
                Funded by: ERA-NET (F4T)
                Funded by: EC | European Research Council (ERC)
                Award ID: 501100000781
                Award ID: COG 617142
                Funded by: Howard Hughes Medical Institute (HHMI)
                Award ID: 100000011
                Award ID: IEC 55007415
                Categories
                8
                8.1
                New Research
                Sensory and Motor Systems
                Custom metadata
                March/April 2017

                learning,motor skill,rna pol ii,rpb1,striatum
                learning, motor skill, rna pol ii, rpb1, striatum

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