دورية أكاديمية
Histone H1 regulates non-coding RNA turnover on chromatin in a m6A-dependent manner.
العنوان: | Histone H1 regulates non-coding RNA turnover on chromatin in a m6A-dependent manner. |
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المؤلفون: | Fernández-Justel JM; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Santa-María C; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Martín-Vírgala S; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Ramesh S; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Ferrera-Lagoa A; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Salinas-Pena M; Instituto de Biología Molecular de Barcelona (IBMB-CSIC), Carrer de Baldiri Reixac, 15, 08028 Barcelona, Spain., Isoler-Alcaraz J; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain., Maslon MM; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe South Road, Edinburgh EH4 2XU, UK., Jordan A; Instituto de Biología Molecular de Barcelona (IBMB-CSIC), Carrer de Baldiri Reixac, 15, 08028 Barcelona, Spain., Cáceres JF; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe South Road, Edinburgh EH4 2XU, UK., Gómez M; Centro de Biología Molecular Severo Ochoa (CBMSO), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Nicolás Cabrera 1, 28049 Madrid, Spain. Electronic address: mgomez@cbm.csic.es. |
المصدر: | Cell reports [Cell Rep] 2022 Sep 13; Vol. 40 (11), pp. 111329. |
نوع المنشور: | Journal Article; Research Support, Non-U.S. Gov't |
اللغة: | English |
بيانات الدورية: | Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print Cited Medium: Internet ISSN: 2211-1247 (Electronic) NLM ISO Abbreviation: Cell Rep Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: [Cambridge, MA] : Cell Press, c 2012- |
مواضيع طبية MeSH: | Chromatin* , Histones*/metabolism, Methylation ; RNA, Untranslated/genetics ; RNA, Untranslated/metabolism ; Transcription Factors/metabolism |
مستخلص: | Linker histones are highly abundant chromatin-associated proteins with well-established structural roles in chromatin and as general transcriptional repressors. In addition, it has been long proposed that histone H1 exerts context-specific effects on gene expression. Here, we identify a function of histone H1 in chromatin structure and transcription using a range of genomic approaches. In the absence of histone H1, there is an increase in the transcription of non-coding RNAs, together with reduced levels of m6A modification leading to their accumulation on chromatin and causing replication-transcription conflicts. This strongly suggests that histone H1 prevents non-coding RNA transcription and regulates non-coding transcript turnover on chromatin. Accordingly, altering the m6A RNA methylation pathway rescues the replicative phenotype of H1 loss. This work unveils unexpected regulatory roles of histone H1 on non-coding RNA turnover and m6A deposition, highlighting the intimate relationship between chromatin conformation, RNA metabolism, and DNA replication to maintain genome performance. Competing Interests: Declaration of interests The authors declare no competing interests. (Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.) |
References: | Nat Commun. 2018 Apr 23;9(1):1590. (PMID: 29686321) Nat Commun. 2019 Jul 16;10(1):3129. (PMID: 31311937) Int J Biochem Cell Biol. 1997 Dec;29(12):1463-6. (PMID: 9570139) PLoS Biol. 2018 Sep 13;16(9):e2006092. (PMID: 30212448) J Biol Chem. 2001 Apr 27;276(17):13587-92. (PMID: 11278859) Nature. 2016 Sep 15;537(7620):369-373. (PMID: 27602518) Cell. 2005 Dec 29;123(7):1199-212. (PMID: 16377562) J Biol Chem. 2005 Sep 16;280(37):32141-7. (PMID: 16006555) Genome Biol. 2009;10(3):R25. (PMID: 19261174) Cell Rep. 2015 Aug 18;12(7):1089-98. (PMID: 26257179) Nucleic Acids Res. 2013 Apr;41(7):4026-35. (PMID: 23435226) Nat Biotechnol. 2010 May;28(5):511-5. (PMID: 20436464) Int J Dev Biol. 2013;57(9-10):725-9. (PMID: 24395560) PLoS Genet. 2008 Oct;4(10):e1000227. (PMID: 18927631) Mol Biol Cell. 2004 Aug;15(8):3876-90. (PMID: 15169873) Cell. 1996 Aug 9;86(3):475-83. (PMID: 8756729) Nucleic Acids Res. 2012 Jul;40(12):5402-14. (PMID: 22406835) FEBS J. 2021 Mar;288(6):1989-2013. (PMID: 32896099) Genome Biol. 2014;15(12):550. (PMID: 25516281) Nature. 2021 Mar;591(7849):322-326. (PMID: 33658714) Elife. 2017 Oct 06;6:. (PMID: 28984244) Nature. 2021 Jan;589(7841):299-305. (PMID: 33299181) Cell. 2019 Oct 17;179(3):604-618. (PMID: 31607512) Nat Rev Genet. 2020 Feb;21(2):102-117. (PMID: 31729473) PLoS Genet. 2013;9(4):e1003417. (PMID: 23633960) J Biol Chem. 2004 Mar 5;279(10):8701-7. (PMID: 14668337) Nucleic Acids Res. 2014 Apr;42(7):4474-93. (PMID: 24476918) Nat Genet. 2020 Jan;52(1):48-55. (PMID: 31844323) BMC Biochem. 2016 Oct 1;17(1):18. (PMID: 27716023) Nucleic Acids Res. 2010 Jun;38(11):3533-45. (PMID: 20156997) Nat Rev Mol Cell Biol. 2019 Oct;20(10):608-624. (PMID: 31520073) EMBO J. 2019 May 2;38(9):. (PMID: 30988016) Mol Cell. 2016 Feb 18;61(4):507-519. (PMID: 26876937) Genome Res. 2021 Aug;31(8):1395-1408. (PMID: 34131006) Clin Epigenetics. 2020 Jan 7;12(1):7. (PMID: 31910894) Cell Rep. 2013 Jun 27;3(6):2142-54. (PMID: 23746450) Nature. 2019 Jul;571(7765):424-428. (PMID: 31292544) Cell Rep. 2019 Oct 29;29(5):1369-1380.e5. (PMID: 31665646) Nature. 2021 Jan;589(7841):293-298. (PMID: 33299182) Nature. 2015 Oct 22;526(7574):525-30. (PMID: 26466571) Mol Cell Biol. 2001 Dec;21(23):7933-43. (PMID: 11689686) EMBO Rep. 2015 Nov;16(11):1439-53. (PMID: 26474902) PLoS Genet. 2012;8(5):e1002691. (PMID: 22589736) PLoS Biol. 2022 Nov 28;20(11):e3001885. (PMID: 36441764) Cell. 2017 Oct 5;171(2):481-494.e15. (PMID: 28985567) Nucleic Acids Res. 2012 Feb;40(4):1475-84. (PMID: 22021384) Genome Biol. 2008;9(9):R137. (PMID: 18798982) Sci Rep. 2015 Nov 19;5:16714. (PMID: 26581166) Nucleic Acids Res. 2017 Nov 16;45(20):11622-11642. (PMID: 28977426) J Biol Chem. 2008 Apr 4;283(14):9113-26. (PMID: 18258596) Nat Protoc. 2019 Mar;14(3):703-721. (PMID: 30804569) Nucleic Acids Res. 2016 Jan 4;44(D1):D164-71. (PMID: 26438538) Science. 2016 Jun 3;352(6290):1225-8. (PMID: 27257258) Cell Rep. 2013 Dec 26;5(6):1690-703. (PMID: 24360965) Cell. 2012 Jun 22;149(7):1635-46. (PMID: 22608085) Nat Rev Mol Cell Biol. 2018 Mar;19(3):192-206. (PMID: 29018282) Cancer Cell. 2021 Jul 12;39(7):958-972.e8. (PMID: 34048709) Chromosome Res. 2006;14(1):17-25. (PMID: 16506093) Nucleic Acids Res. 2016 Jul 8;44(W1):W90-7. (PMID: 27141961) Genome Biol. 2013 Apr 25;14(4):R36. (PMID: 23618408) Cell Rep. 2016 Feb 9;14(5):1246-1257. (PMID: 26832418) Biochim Biophys Acta. 2016 Mar;1859(3):455-61. (PMID: 26455956) Proc Natl Acad Sci U S A. 2020 Jun 23;117(25):14251-14258. (PMID: 32513732) Science. 2004 Jun 11;304(5677):1675-8. (PMID: 15192231) Nat Struct Mol Biol. 2017 Jul;24(7):596-603. (PMID: 28628087) Bioinformatics. 2009 Aug 15;25(16):2078-9. (PMID: 19505943) J Cell Biol. 1998 Mar 23;140(6):1285-95. (PMID: 9508763) Nat Methods. 2017 Apr;14(4):417-419. (PMID: 28263959) Nature. 2021 Mar;591(7849):317-321. (PMID: 33505026) Genome Biol. 2015 Dec 23;16:289. (PMID: 26700097) PLoS One. 2014 Dec 08;9(12):e114485. (PMID: 25486255) Cell Rep. 2016 Sep 27;17(1):19-28. (PMID: 27681417) Science. 2020 Jan 31;367(6477):580-586. (PMID: 31949099) J Mol Biol. 2015 Jun 5;427(11):2056-71. (PMID: 25584861) |
معلومات مُعتمدة: | MC_UU_00007/7 United Kingdom MRC_ Medical Research Council |
فهرسة مساهمة: | Keywords: CP: Molecular biology; R-loops; chromatin RNAs; chromatin conformation; histone H1; lncRNAs; m6A; mESCs; replication-transcription conflicts; replicative stress |
المشرفين على المادة: | 0 (Chromatin) 0 (Histones) 0 (RNA, Untranslated) 0 (Transcription Factors) |
تواريخ الأحداث: | Date Created: 20220914 Date Completed: 20220916 Latest Revision: 20240905 |
رمز التحديث: | 20240905 |
مُعرف محوري في PubMed: | PMC7613722 |
DOI: | 10.1016/j.celrep.2022.111329 |
PMID: | 36103831 |
قاعدة البيانات: | MEDLINE |
تدمد: | 2211-1247 |
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DOI: | 10.1016/j.celrep.2022.111329 |