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An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus

Endogenous bornavirus-like L (EBLL) elements are inheritable sequences derived from ancient bornavirus L genes that encode a viral RNA-dependent RNA polymerase (RdRp) in many eukaryotic genomes. Here, we demonstrate that bats of the genus Eptesicus have preserved for more than 11.8 million years an...

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Autores principales: Horie, Masayuki, Kobayashi, Yuki, Honda, Tomoyuki, Fujino, Kan, Akasaka, Takumi, Kohl, Claudia, Wibbelt, Gudrun, Mühldorfer, Kristin, Kurth, Andreas, Müller, Marcel A., Corman, Victor M., Gillich, Nadine, Suzuki, Yoshiyuki, Schwemmle, Martin, Tomonaga, Keizo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865735/
https://www.ncbi.nlm.nih.gov/pubmed/27174689
http://dx.doi.org/10.1038/srep25873
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author Horie, Masayuki
Kobayashi, Yuki
Honda, Tomoyuki
Fujino, Kan
Akasaka, Takumi
Kohl, Claudia
Wibbelt, Gudrun
Mühldorfer, Kristin
Kurth, Andreas
Müller, Marcel A.
Corman, Victor M.
Gillich, Nadine
Suzuki, Yoshiyuki
Schwemmle, Martin
Tomonaga, Keizo
author_facet Horie, Masayuki
Kobayashi, Yuki
Honda, Tomoyuki
Fujino, Kan
Akasaka, Takumi
Kohl, Claudia
Wibbelt, Gudrun
Mühldorfer, Kristin
Kurth, Andreas
Müller, Marcel A.
Corman, Victor M.
Gillich, Nadine
Suzuki, Yoshiyuki
Schwemmle, Martin
Tomonaga, Keizo
author_sort Horie, Masayuki
collection PubMed
description Endogenous bornavirus-like L (EBLL) elements are inheritable sequences derived from ancient bornavirus L genes that encode a viral RNA-dependent RNA polymerase (RdRp) in many eukaryotic genomes. Here, we demonstrate that bats of the genus Eptesicus have preserved for more than 11.8 million years an EBLL element named eEBLL-1, which has an intact open reading frame of 1,718 codons. The eEBLL-1 coding sequence revealed that functional motifs essential for mononegaviral RdRp activity are well conserved in the EBLL-1 genes. Genetic analyses showed that natural selection operated on eEBLL-1 during the evolution of Eptesicus. Notably, we detected efficient transcription of eEBLL-1 in tissues from Eptesicus bats. To the best of our knowledge, this study is the first report showing that the eukaryotic genome has gained a riboviral polymerase gene from an ancient virus that has the potential to encode a functional RdRp.
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spelling pubmed-48657352016-05-23 An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus Horie, Masayuki Kobayashi, Yuki Honda, Tomoyuki Fujino, Kan Akasaka, Takumi Kohl, Claudia Wibbelt, Gudrun Mühldorfer, Kristin Kurth, Andreas Müller, Marcel A. Corman, Victor M. Gillich, Nadine Suzuki, Yoshiyuki Schwemmle, Martin Tomonaga, Keizo Sci Rep Article Endogenous bornavirus-like L (EBLL) elements are inheritable sequences derived from ancient bornavirus L genes that encode a viral RNA-dependent RNA polymerase (RdRp) in many eukaryotic genomes. Here, we demonstrate that bats of the genus Eptesicus have preserved for more than 11.8 million years an EBLL element named eEBLL-1, which has an intact open reading frame of 1,718 codons. The eEBLL-1 coding sequence revealed that functional motifs essential for mononegaviral RdRp activity are well conserved in the EBLL-1 genes. Genetic analyses showed that natural selection operated on eEBLL-1 during the evolution of Eptesicus. Notably, we detected efficient transcription of eEBLL-1 in tissues from Eptesicus bats. To the best of our knowledge, this study is the first report showing that the eukaryotic genome has gained a riboviral polymerase gene from an ancient virus that has the potential to encode a functional RdRp. Nature Publishing Group 2016-05-13 /pmc/articles/PMC4865735/ /pubmed/27174689 http://dx.doi.org/10.1038/srep25873 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Horie, Masayuki
Kobayashi, Yuki
Honda, Tomoyuki
Fujino, Kan
Akasaka, Takumi
Kohl, Claudia
Wibbelt, Gudrun
Mühldorfer, Kristin
Kurth, Andreas
Müller, Marcel A.
Corman, Victor M.
Gillich, Nadine
Suzuki, Yoshiyuki
Schwemmle, Martin
Tomonaga, Keizo
An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title_full An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title_fullStr An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title_full_unstemmed An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title_short An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus
title_sort rna-dependent rna polymerase gene in bat genomes derived from an ancient negative-strand rna virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865735/
https://www.ncbi.nlm.nih.gov/pubmed/27174689
http://dx.doi.org/10.1038/srep25873
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