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Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy

Inflorescence structure is very diverse and homoplasious, yet the developmental basis of their homoplasy is poorly understood. To gain an understanding of the degree of homology that these diverse structures share, we characterize the developmental morphology and anatomy of various umbellate inflore...

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Autores principales: Martínez-Gómez, Jesús, Atluri, Tara A. M., Rose, Irving Jason, Holliday, Aaliyah J., Strock, Christopher F., Lynch, Jonathan P., Miller, William B., Stevenson, Dennis Wm., Specht, Chelsea D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100582/
https://www.ncbi.nlm.nih.gov/pubmed/35574142
http://dx.doi.org/10.3389/fpls.2022.873505
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author Martínez-Gómez, Jesús
Atluri, Tara A. M.
Rose, Irving Jason
Holliday, Aaliyah J.
Strock, Christopher F.
Lynch, Jonathan P.
Miller, William B.
Stevenson, Dennis Wm.
Specht, Chelsea D.
author_facet Martínez-Gómez, Jesús
Atluri, Tara A. M.
Rose, Irving Jason
Holliday, Aaliyah J.
Strock, Christopher F.
Lynch, Jonathan P.
Miller, William B.
Stevenson, Dennis Wm.
Specht, Chelsea D.
author_sort Martínez-Gómez, Jesús
collection PubMed
description Inflorescence structure is very diverse and homoplasious, yet the developmental basis of their homoplasy is poorly understood. To gain an understanding of the degree of homology that these diverse structures share, we characterize the developmental morphology and anatomy of various umbellate inflorescences across the monocots and analyzed them in an evolutionary context. To characterize branching order, we characterized the developmental morphology of multiple inflorescences with epi-illumination, and vascular anatomy with Laser Ablation Tomography, a novel high-throughput method to reconstruct three-dimensional vasculature. We used these approaches to analyze the umbellate inflorescences in five instances of presumed homoplasy: in three members of the Amaryllidaceae; in three members of the Asparagaceae, including a putatively derived raceme in Dichelostemma congestum; in Butomus umbellatus (Alismataceae), in Tacca chantrieri (Dioscoreaceae), and in umbellate structure in Fritillaria imperialis (Liliaceae). We compare these with racemes found in three members of the subfamily Scilliioideae (Asparagaceae). We find there are three convergent developmental programs that generate umbellate inflorescences in the monocots, bostryx-derived, cincinnus-derived and raceme-derived. Additionally, among the bostryx-derived umbellate inflorescence, there are three instances of parallel evolution found in the Amaryllidaceae, in two members of Brodiaeoideae (Asparagaceae), and Butomus umbellatus, all of which share the same generative developmental program. We discuss the morphological modifications necessary to generate such complex and condensed structures and use these insights to describe a new variant of metatopy, termed horizontal concaulesence. We contextualize our findings within the broader literature of monocot inflorescence development, with a focus on synthesizing descriptive developmental morphological studies.
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spelling pubmed-91005822022-05-14 Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy Martínez-Gómez, Jesús Atluri, Tara A. M. Rose, Irving Jason Holliday, Aaliyah J. Strock, Christopher F. Lynch, Jonathan P. Miller, William B. Stevenson, Dennis Wm. Specht, Chelsea D. Front Plant Sci Plant Science Inflorescence structure is very diverse and homoplasious, yet the developmental basis of their homoplasy is poorly understood. To gain an understanding of the degree of homology that these diverse structures share, we characterize the developmental morphology and anatomy of various umbellate inflorescences across the monocots and analyzed them in an evolutionary context. To characterize branching order, we characterized the developmental morphology of multiple inflorescences with epi-illumination, and vascular anatomy with Laser Ablation Tomography, a novel high-throughput method to reconstruct three-dimensional vasculature. We used these approaches to analyze the umbellate inflorescences in five instances of presumed homoplasy: in three members of the Amaryllidaceae; in three members of the Asparagaceae, including a putatively derived raceme in Dichelostemma congestum; in Butomus umbellatus (Alismataceae), in Tacca chantrieri (Dioscoreaceae), and in umbellate structure in Fritillaria imperialis (Liliaceae). We compare these with racemes found in three members of the subfamily Scilliioideae (Asparagaceae). We find there are three convergent developmental programs that generate umbellate inflorescences in the monocots, bostryx-derived, cincinnus-derived and raceme-derived. Additionally, among the bostryx-derived umbellate inflorescence, there are three instances of parallel evolution found in the Amaryllidaceae, in two members of Brodiaeoideae (Asparagaceae), and Butomus umbellatus, all of which share the same generative developmental program. We discuss the morphological modifications necessary to generate such complex and condensed structures and use these insights to describe a new variant of metatopy, termed horizontal concaulesence. We contextualize our findings within the broader literature of monocot inflorescence development, with a focus on synthesizing descriptive developmental morphological studies. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9100582/ /pubmed/35574142 http://dx.doi.org/10.3389/fpls.2022.873505 Text en Copyright © 2022 Martínez-Gómez, Atluri, Rose, Holliday, Strock, Lynch, Miller, Stevenson and Specht. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Martínez-Gómez, Jesús
Atluri, Tara A. M.
Rose, Irving Jason
Holliday, Aaliyah J.
Strock, Christopher F.
Lynch, Jonathan P.
Miller, William B.
Stevenson, Dennis Wm.
Specht, Chelsea D.
Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title_full Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title_fullStr Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title_full_unstemmed Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title_short Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy
title_sort developmental morphology and anatomy shed light on both parallel and convergent evolution of the umbellate inflorescence in monocots, underlain by a new variant of metatopy
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100582/
https://www.ncbi.nlm.nih.gov/pubmed/35574142
http://dx.doi.org/10.3389/fpls.2022.873505
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