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Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement

Genes for the plastid-encoded RNA polymerase (PEP) persist in the plastid genomes of all photosynthetic angiosperms. However, three unrelated lineages (Annonaceae, Passifloraceae and Geraniaceae) have been identified with unusually divergent open reading frames (ORFs) in the conserved region of rpoA...

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Autores principales: Blazier, J. Chris, Ruhlman, Tracey A., Weng, Mao-Lun, Rehman, Sumaiyah K., Sabir, Jamal S. M., Jansen, Robert K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834550/
https://www.ncbi.nlm.nih.gov/pubmed/27087667
http://dx.doi.org/10.1038/srep24595
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author Blazier, J. Chris
Ruhlman, Tracey A.
Weng, Mao-Lun
Rehman, Sumaiyah K.
Sabir, Jamal S. M.
Jansen, Robert K.
author_facet Blazier, J. Chris
Ruhlman, Tracey A.
Weng, Mao-Lun
Rehman, Sumaiyah K.
Sabir, Jamal S. M.
Jansen, Robert K.
author_sort Blazier, J. Chris
collection PubMed
description Genes for the plastid-encoded RNA polymerase (PEP) persist in the plastid genomes of all photosynthetic angiosperms. However, three unrelated lineages (Annonaceae, Passifloraceae and Geraniaceae) have been identified with unusually divergent open reading frames (ORFs) in the conserved region of rpoA, the gene encoding the PEP α subunit. We used sequence-based approaches to evaluate whether these genes retain function. Both gene sequences and complete plastid genome sequences were assembled and analyzed from each of the three angiosperm families. Multiple lines of evidence indicated that the rpoA sequences are likely functional despite retaining as low as 30% nucleotide sequence identity with rpoA genes from outgroups in the same angiosperm order. The ratio of non-synonymous to synonymous substitutions indicated that these genes are under purifying selection, and bioinformatic prediction of conserved domains indicated that functional domains are preserved. One of the lineages (Pelargonium, Geraniaceae) contains species with multiple rpoA-like ORFs that show evidence of ongoing inter-paralog gene conversion. The plastid genomes containing these divergent rpoA genes have experienced extensive structural rearrangement, including large expansions of the inverted repeat. We propose that illegitimate recombination, not positive selection, has driven the divergence of rpoA.
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spelling pubmed-48345502016-04-27 Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement Blazier, J. Chris Ruhlman, Tracey A. Weng, Mao-Lun Rehman, Sumaiyah K. Sabir, Jamal S. M. Jansen, Robert K. Sci Rep Article Genes for the plastid-encoded RNA polymerase (PEP) persist in the plastid genomes of all photosynthetic angiosperms. However, three unrelated lineages (Annonaceae, Passifloraceae and Geraniaceae) have been identified with unusually divergent open reading frames (ORFs) in the conserved region of rpoA, the gene encoding the PEP α subunit. We used sequence-based approaches to evaluate whether these genes retain function. Both gene sequences and complete plastid genome sequences were assembled and analyzed from each of the three angiosperm families. Multiple lines of evidence indicated that the rpoA sequences are likely functional despite retaining as low as 30% nucleotide sequence identity with rpoA genes from outgroups in the same angiosperm order. The ratio of non-synonymous to synonymous substitutions indicated that these genes are under purifying selection, and bioinformatic prediction of conserved domains indicated that functional domains are preserved. One of the lineages (Pelargonium, Geraniaceae) contains species with multiple rpoA-like ORFs that show evidence of ongoing inter-paralog gene conversion. The plastid genomes containing these divergent rpoA genes have experienced extensive structural rearrangement, including large expansions of the inverted repeat. We propose that illegitimate recombination, not positive selection, has driven the divergence of rpoA. Nature Publishing Group 2016-04-18 /pmc/articles/PMC4834550/ /pubmed/27087667 http://dx.doi.org/10.1038/srep24595 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
Blazier, J. Chris
Ruhlman, Tracey A.
Weng, Mao-Lun
Rehman, Sumaiyah K.
Sabir, Jamal S. M.
Jansen, Robert K.
Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title_full Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title_fullStr Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title_full_unstemmed Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title_short Divergence of RNA polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
title_sort divergence of rna polymerase α subunits in angiosperm plastid genomes is mediated by genomic rearrangement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834550/
https://www.ncbi.nlm.nih.gov/pubmed/27087667
http://dx.doi.org/10.1038/srep24595
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