Identification and Characterization of Base-Substitution Mutations in the Macronuclear Genome of the Ciliate Tetrahymena thermophila.


Journal

Genome biology and evolution
ISSN: 1759-6653
Titre abrégé: Genome Biol Evol
Pays: England
ID NLM: 101509707

Informations de publication

Date de publication:
07 01 2021
Historique:
accepted: 28 10 2020
pubmed: 5 11 2020
medline: 18 11 2021
entrez: 4 11 2020
Statut: ppublish

Résumé

Polyploidy can provide adaptive advantages and drive evolution. Amitotic division of the polyploid macronucleus (MAC) in ciliates acts as a nonsexual genetic mechanism to enhance adaptation to stress conditions and thus provides a unique model to investigate the evolutionary role of polyploidy. Mutation is the primary source of the variation responsible for evolution and adaptation; however, to date, de novo mutations that occur in ciliate MAC genomes during these processes have not been characterized and their biological impacts are undefined. Here, we carried out long-term evolution experiments to directly explore de novo MAC mutations and their molecular features in the model ciliate, Tetrahymena thermophila. A simple but effective method was established to detect base-substitution mutations in evolving populations whereas filtering out most of the false positive base-substitutions caused by repetitive sequences and the programmed genome rearrangements. The detected mutations were rigorously validated using the MassARRAY system. Validated mutations showed a strong G/C→A/T bias, consistent with observations in other species. Moreover, a progressive increase in growth rate of the evolving populations suggested that some of these mutations might be responsible for cell fitness. The established mutation identification and validation methods will be an invaluable resource to make ciliates an important model system to study the role of polyploidy in evolution.

Identifiants

pubmed: 33146387
pii: 5955769
doi: 10.1093/gbe/evaa232
pmc: PMC7788487
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

Références

Plant Biotechnol J. 2014 Jan;12(1):28-37
pubmed: 24034357
Bioinformatics. 2014 Oct 15;30(20):2843-51
pubmed: 24974202
Nucleic Acids Res. 2008 Sep;36(16):e105
pubmed: 18660515
Microbiol Rev. 1994 Jun;58(2):233-67
pubmed: 8078435
Methods Cell Biol. 1975;9(0):311-27
pubmed: 805898
Genome Biol. 2007;8(7):R143
pubmed: 17659080
Nature. 1980 Oct 9;287(5782):560-1
pubmed: 6999365
Fly (Austin). 2012 Apr-Jun;6(2):80-92
pubmed: 22728672
Genome Biol Evol. 2016 Dec 1;8(12):3629-3639
pubmed: 27635054
BMC Evol Biol. 2014 May 28;14:112
pubmed: 24885485
Diagn Pathol. 2015 Jul 30;10:132
pubmed: 26220423
PLoS Biol. 2006 Sep;4(9):e286
pubmed: 16933976
Nat Rev Genet. 2013 Dec;14(12):827-39
pubmed: 24166031
Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9272-7
pubmed: 18583475
Nat Rev Genet. 2012 Feb 14;13(3):204-14
pubmed: 22330764
J Eukaryot Microbiol. 2019 Nov;66(6):954-965
pubmed: 31188517
PLoS Biol. 2005 Oct;3(10):e334
pubmed: 16176121
Mech Ageing Dev. 1975 May-Aug;4(3-4):263-79
pubmed: 811932
Nat Rev Genet. 2017 Jul;18(7):411-424
pubmed: 28502977
J Clin Invest. 2012 Sep;122(9):3307-15
pubmed: 22863619
J Cell Biol. 2015 May 25;209(4):485-91
pubmed: 26008741
Dev Genet. 1992;13(2):126-32
pubmed: 1499154
BMC Evol Biol. 2010 Nov 15;10:354
pubmed: 21078144
Methods Cell Biol. 2012;109:237-76
pubmed: 22444147
PLoS Genet. 2010 Oct 21;6(10):e1001164
pubmed: 20975944
PLoS Biol. 2019 Jun 3;17(6):e3000294
pubmed: 31158217
J Protozool. 1963 Nov;10:413-20
pubmed: 14074437
Nat Ecol Evol. 2018 Feb;2(2):237-240
pubmed: 29292397
Elife. 2016 Nov 28;5:
pubmed: 27892853
J Cell Sci. 1975 May;17(3):471-93
pubmed: 806605
Genetics. 2013 Oct;195(2):527-40
pubmed: 23934880
Curr Biol. 2013 Nov 18;23(22):2224-2232
pubmed: 24184101
Genome Res. 2010 Feb;20(2):273-80
pubmed: 20019143
Bioinformatics. 2009 Aug 15;25(16):2078-9
pubmed: 19505943
BMC Cancer. 2010 Mar 16;10:101
pubmed: 20233444
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D500-3
pubmed: 16381920
Nat Rev Genet. 2016 Oct 14;17(11):704-714
pubmed: 27739533
Brief Bioinform. 2013 Mar;14(2):178-92
pubmed: 22517427
Anal Chem. 2011 Nov 15;83(22):8604-10
pubmed: 22035192
J Mol Biol. 1990 Oct 5;215(3):403-10
pubmed: 2231712

Auteurs

Guangying Wang (G)

Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.

Lu Fu (L)

Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
University of Chinese Academy of Sciences, Beijing, China.

Jie Xiong (J)

Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.

Kazufumi Mochizuki (K)

Institute of Human Genetics (IGH), CNRS, University of Montpellier, France.

Yunxin Fu (Y)

Department of Biostatistics and Data Science and Human Genetics Center, School of Public Health, The University of Texas Health Science Center.

Wei Miao (W)

Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
University of Chinese Academy of Sciences, Beijing, China.
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
CAS Center for Excellence in Animal Evolution and Genetics, Kunming, China.

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