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Extreme plastomes in holoparasitic Balanophoraceae are not the norm
BACKGROUND: Balanophoraceae plastomes are known for their highly condensed and re-arranged nature alongside the most extreme nucleotide compositional bias known to date, culminating in two independent reconfigurations of their genetic code. Currently, a large portion of the Balanophoraceae diversity...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268348/ https://www.ncbi.nlm.nih.gov/pubmed/37322447 http://dx.doi.org/10.1186/s12864-023-09422-1 |
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author | Kim, Woorin Lautenschläger, Thea Bolin, Jay F. Rees, Mathew Nzuzi, Albertina Zhou, Renchao Wanke, Stefan Jost, Matthias |
author_facet | Kim, Woorin Lautenschläger, Thea Bolin, Jay F. Rees, Mathew Nzuzi, Albertina Zhou, Renchao Wanke, Stefan Jost, Matthias |
author_sort | Kim, Woorin |
collection | PubMed |
description | BACKGROUND: Balanophoraceae plastomes are known for their highly condensed and re-arranged nature alongside the most extreme nucleotide compositional bias known to date, culminating in two independent reconfigurations of their genetic code. Currently, a large portion of the Balanophoraceae diversity remains unexplored, hindering, among others, evolutionary pattern recognition. Here, we explored newly sequenced plastomes of Sarcophyte sanguinea and Thonningia sanguinea. The reconstructed plastomes were analyzed using various methods of comparative genomics based on a representative taxon sampling. RESULTS: Sarcophyte, recovered sister to the other sampled Balanophoraceae s. str., has plastomes up to 50% larger than those currently published. Its gene set contains five genes lost in any other species, including matK. Five cis-spliced introns are maintained. In contrast, the Thonningia plastome is similarly reduced to published Balanophoraceae and retains only a single cis-spliced intron. Its protein-coding genes show a more biased codon usage compared to Sarcophyte, with an accumulation of in-frame TAG stop codons. Structural plastome comparison revealed multiple, previously unknown, structural rearrangements within Balanophoraceae. CONCLUSIONS: For the “minimal plastomes” of Thonningia, we propose a genetic code change identical to sister genus Balanophora. Sarcophyte however differs drastically from our current understanding on Balanophoraceae plastomes. With a less-extreme nucleotide composition, there is no evidence for an altered genetic code. Using comparative genomics, we identified a hotspot for plastome reconfiguration in Balanophoraceae. Based on previously published and newly identified structural reconfigurations, we propose an updated model of evolutionary plastome trajectories for Balanophoraceae, illustrating a much greater plastome diversity than previously known. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09422-1. |
format | Online Article Text |
id | pubmed-10268348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102683482023-06-15 Extreme plastomes in holoparasitic Balanophoraceae are not the norm Kim, Woorin Lautenschläger, Thea Bolin, Jay F. Rees, Mathew Nzuzi, Albertina Zhou, Renchao Wanke, Stefan Jost, Matthias BMC Genomics Research BACKGROUND: Balanophoraceae plastomes are known for their highly condensed and re-arranged nature alongside the most extreme nucleotide compositional bias known to date, culminating in two independent reconfigurations of their genetic code. Currently, a large portion of the Balanophoraceae diversity remains unexplored, hindering, among others, evolutionary pattern recognition. Here, we explored newly sequenced plastomes of Sarcophyte sanguinea and Thonningia sanguinea. The reconstructed plastomes were analyzed using various methods of comparative genomics based on a representative taxon sampling. RESULTS: Sarcophyte, recovered sister to the other sampled Balanophoraceae s. str., has plastomes up to 50% larger than those currently published. Its gene set contains five genes lost in any other species, including matK. Five cis-spliced introns are maintained. In contrast, the Thonningia plastome is similarly reduced to published Balanophoraceae and retains only a single cis-spliced intron. Its protein-coding genes show a more biased codon usage compared to Sarcophyte, with an accumulation of in-frame TAG stop codons. Structural plastome comparison revealed multiple, previously unknown, structural rearrangements within Balanophoraceae. CONCLUSIONS: For the “minimal plastomes” of Thonningia, we propose a genetic code change identical to sister genus Balanophora. Sarcophyte however differs drastically from our current understanding on Balanophoraceae plastomes. With a less-extreme nucleotide composition, there is no evidence for an altered genetic code. Using comparative genomics, we identified a hotspot for plastome reconfiguration in Balanophoraceae. Based on previously published and newly identified structural reconfigurations, we propose an updated model of evolutionary plastome trajectories for Balanophoraceae, illustrating a much greater plastome diversity than previously known. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09422-1. BioMed Central 2023-06-15 /pmc/articles/PMC10268348/ /pubmed/37322447 http://dx.doi.org/10.1186/s12864-023-09422-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kim, Woorin Lautenschläger, Thea Bolin, Jay F. Rees, Mathew Nzuzi, Albertina Zhou, Renchao Wanke, Stefan Jost, Matthias Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title | Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title_full | Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title_fullStr | Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title_full_unstemmed | Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title_short | Extreme plastomes in holoparasitic Balanophoraceae are not the norm |
title_sort | extreme plastomes in holoparasitic balanophoraceae are not the norm |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268348/ https://www.ncbi.nlm.nih.gov/pubmed/37322447 http://dx.doi.org/10.1186/s12864-023-09422-1 |
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