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NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss
BACKGROUND: Key innovations have facilitated novel niche utilization, such as the movement of the algal predecessors of land plants into terrestrial habitats where drastic fluctuations in light intensity, ultraviolet radiation and water limitation required a number of adaptations. The NDH (NADH dehy...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404220/ https://www.ncbi.nlm.nih.gov/pubmed/25886915 http://dx.doi.org/10.1186/s12870-015-0484-7 |
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author | Ruhlman, Tracey A Chang, Wan-Jung Chen, Jeremy JW Huang, Yao-Ting Chan, Ming-Tsair Zhang, Jin Liao, De-Chih Blazier, John C Jin, Xiaohua Shih, Ming-Che Jansen, Robert K Lin, Choun-Sea |
author_facet | Ruhlman, Tracey A Chang, Wan-Jung Chen, Jeremy JW Huang, Yao-Ting Chan, Ming-Tsair Zhang, Jin Liao, De-Chih Blazier, John C Jin, Xiaohua Shih, Ming-Che Jansen, Robert K Lin, Choun-Sea |
author_sort | Ruhlman, Tracey A |
collection | PubMed |
description | BACKGROUND: Key innovations have facilitated novel niche utilization, such as the movement of the algal predecessors of land plants into terrestrial habitats where drastic fluctuations in light intensity, ultraviolet radiation and water limitation required a number of adaptations. The NDH (NADH dehydrogenase-like) complex of Viridiplantae plastids participates in adapting the photosynthetic response to environmental stress, suggesting its involvement in the transition to terrestrial habitats. Although relatively rare, the loss or pseudogenization of plastid NDH genes is widely distributed across diverse lineages of photoautotrophic seed plants and mutants/transgenics lacking NDH function demonstrate little difference from wild type under non-stressed conditions. This study analyzes large transcriptomic and genomic datasets to evaluate the persistence and loss of NDH expression across plants. RESULTS: Nuclear expression profiles showed accretion of the NDH gene complement at key transitions in land plant evolution, such as the transition to land and at the base of the angiosperm lineage. While detection of transcripts for a selection of non-NDH, photosynthesis related proteins was independent of the state of NDH, coordinate, lineage-specific loss of plastid NDH genes and expression of nuclear-encoded NDH subunits was documented in Pinaceae, gnetophytes, Orchidaceae and Geraniales confirming the independent and complete loss of NDH in these diverse seed plant taxa. CONCLUSION: The broad phylogenetic distribution of NDH loss and the subtle phenotypes of mutants suggest that the NDH complex is of limited biological significance in contemporary plants. While NDH activity appears dispensable under favorable conditions, there were likely sufficiently frequent episodes of abiotic stress affecting terrestrial habitats to allow the retention of NDH activity. These findings reveal genetic factors influencing plant/environment interactions in a changing climate through 450 million years of land plant evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0484-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4404220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44042202015-04-21 NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss Ruhlman, Tracey A Chang, Wan-Jung Chen, Jeremy JW Huang, Yao-Ting Chan, Ming-Tsair Zhang, Jin Liao, De-Chih Blazier, John C Jin, Xiaohua Shih, Ming-Che Jansen, Robert K Lin, Choun-Sea BMC Plant Biol Research Article BACKGROUND: Key innovations have facilitated novel niche utilization, such as the movement of the algal predecessors of land plants into terrestrial habitats where drastic fluctuations in light intensity, ultraviolet radiation and water limitation required a number of adaptations. The NDH (NADH dehydrogenase-like) complex of Viridiplantae plastids participates in adapting the photosynthetic response to environmental stress, suggesting its involvement in the transition to terrestrial habitats. Although relatively rare, the loss or pseudogenization of plastid NDH genes is widely distributed across diverse lineages of photoautotrophic seed plants and mutants/transgenics lacking NDH function demonstrate little difference from wild type under non-stressed conditions. This study analyzes large transcriptomic and genomic datasets to evaluate the persistence and loss of NDH expression across plants. RESULTS: Nuclear expression profiles showed accretion of the NDH gene complement at key transitions in land plant evolution, such as the transition to land and at the base of the angiosperm lineage. While detection of transcripts for a selection of non-NDH, photosynthesis related proteins was independent of the state of NDH, coordinate, lineage-specific loss of plastid NDH genes and expression of nuclear-encoded NDH subunits was documented in Pinaceae, gnetophytes, Orchidaceae and Geraniales confirming the independent and complete loss of NDH in these diverse seed plant taxa. CONCLUSION: The broad phylogenetic distribution of NDH loss and the subtle phenotypes of mutants suggest that the NDH complex is of limited biological significance in contemporary plants. While NDH activity appears dispensable under favorable conditions, there were likely sufficiently frequent episodes of abiotic stress affecting terrestrial habitats to allow the retention of NDH activity. These findings reveal genetic factors influencing plant/environment interactions in a changing climate through 450 million years of land plant evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0484-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-11 /pmc/articles/PMC4404220/ /pubmed/25886915 http://dx.doi.org/10.1186/s12870-015-0484-7 Text en © Ruhlman et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ruhlman, Tracey A Chang, Wan-Jung Chen, Jeremy JW Huang, Yao-Ting Chan, Ming-Tsair Zhang, Jin Liao, De-Chih Blazier, John C Jin, Xiaohua Shih, Ming-Che Jansen, Robert K Lin, Choun-Sea NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title | NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title_full | NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title_fullStr | NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title_full_unstemmed | NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title_short | NDH expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
title_sort | ndh expression marks major transitions in plant evolution and reveals coordinate intracellular gene loss |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404220/ https://www.ncbi.nlm.nih.gov/pubmed/25886915 http://dx.doi.org/10.1186/s12870-015-0484-7 |
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