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Stepwise and independent origins of roots among land plants

Roots are one of the three fundamental organ systems of vascular plants1, where they play roles in anchorage, symbiosis, nutrient and water uptake2–4. However, the fragmentary nature of the fossil record obscures their origins and makes it difficult to identify the sole defining characteristic of ex...

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Autores principales: Hetherington, Alexander J., Dolan, Liam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175059/
https://www.ncbi.nlm.nih.gov/pubmed/30135586
http://dx.doi.org/10.1038/s41586-018-0445-z
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author Hetherington, Alexander J.
Dolan, Liam
author_facet Hetherington, Alexander J.
Dolan, Liam
author_sort Hetherington, Alexander J.
collection PubMed
description Roots are one of the three fundamental organ systems of vascular plants1, where they play roles in anchorage, symbiosis, nutrient and water uptake2–4. However, the fragmentary nature of the fossil record obscures their origins and makes it difficult to identify the sole defining characteristic of extant roots – the presence of self-renewing structures called root meristems covered by a root cap at their apex1–9. Here we report the discovery of the oldest meristems of rooting axes preserved in the 407 million year old Rhynie chert, the earliest preserved terrestrial ecosystem10. These meristems, of the lycopsid Asteroxylon mackiei11–14, lacked root caps and instead developed a continuous epidermis over the surface of the meristem. A. mackiei rooting axes and meristems are therefore unique among vascular plants. These data support the hypothesis that roots, as defined in extant vascular plants by the presence of a root cap7, were a late innovation in the vascular lineage. Roots therefore acquired traits in a stepwise fashion. The relatively late origin of roots with caps in lycophytes is consistent with the hypothesis that roots evolved multiple times2, rather than having a single origin1, and the extensive similarities between lycophyte and euphyllophyte roots15–18 therefore represent examples of convergent evolution. The key phylogenetic position of A. mackiei, with its transitional rooting organ, between early diverging land plants that lacked roots and the derived plants that developed roots, demonstrates how roots were “assembled” during the course of plant evolution.
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spelling pubmed-61750592019-03-01 Stepwise and independent origins of roots among land plants Hetherington, Alexander J. Dolan, Liam Nature Article Roots are one of the three fundamental organ systems of vascular plants1, where they play roles in anchorage, symbiosis, nutrient and water uptake2–4. However, the fragmentary nature of the fossil record obscures their origins and makes it difficult to identify the sole defining characteristic of extant roots – the presence of self-renewing structures called root meristems covered by a root cap at their apex1–9. Here we report the discovery of the oldest meristems of rooting axes preserved in the 407 million year old Rhynie chert, the earliest preserved terrestrial ecosystem10. These meristems, of the lycopsid Asteroxylon mackiei11–14, lacked root caps and instead developed a continuous epidermis over the surface of the meristem. A. mackiei rooting axes and meristems are therefore unique among vascular plants. These data support the hypothesis that roots, as defined in extant vascular plants by the presence of a root cap7, were a late innovation in the vascular lineage. Roots therefore acquired traits in a stepwise fashion. The relatively late origin of roots with caps in lycophytes is consistent with the hypothesis that roots evolved multiple times2, rather than having a single origin1, and the extensive similarities between lycophyte and euphyllophyte roots15–18 therefore represent examples of convergent evolution. The key phylogenetic position of A. mackiei, with its transitional rooting organ, between early diverging land plants that lacked roots and the derived plants that developed roots, demonstrates how roots were “assembled” during the course of plant evolution. 2018-08-22 2018-09 /pmc/articles/PMC6175059/ /pubmed/30135586 http://dx.doi.org/10.1038/s41586-018-0445-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Hetherington, Alexander J.
Dolan, Liam
Stepwise and independent origins of roots among land plants
title Stepwise and independent origins of roots among land plants
title_full Stepwise and independent origins of roots among land plants
title_fullStr Stepwise and independent origins of roots among land plants
title_full_unstemmed Stepwise and independent origins of roots among land plants
title_short Stepwise and independent origins of roots among land plants
title_sort stepwise and independent origins of roots among land plants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175059/
https://www.ncbi.nlm.nih.gov/pubmed/30135586
http://dx.doi.org/10.1038/s41586-018-0445-z
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