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Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata

Several Kalanchoë species reproduce asexually by forming plantlets in the leaf crenulations. Some species produce plantlets incessantly via somatic embryogenesis and organogenesis, whereas others exclusively develop plantlets after leaf detachment, presumably through organogenesis. SHOOT MERISTEMLES...

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Autores principales: Jácome-Blásquez, Francisco, Kim, Minsung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200927/
https://www.ncbi.nlm.nih.gov/pubmed/37223821
http://dx.doi.org/10.3389/fpls.2023.1157619
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author Jácome-Blásquez, Francisco
Kim, Minsung
author_facet Jácome-Blásquez, Francisco
Kim, Minsung
author_sort Jácome-Blásquez, Francisco
collection PubMed
description Several Kalanchoë species reproduce asexually by forming plantlets in the leaf crenulations. Some species produce plantlets incessantly via somatic embryogenesis and organogenesis, whereas others exclusively develop plantlets after leaf detachment, presumably through organogenesis. SHOOT MERISTEMLESS (STM), which mediates SAM functions, appears to be involved in Kalanchoë plantlet formation, suggesting that meristem genes may be essential for plantlet formation. However, the genetic regulatory network for establishing and maintaining plantlet primordia in Kalanchoë remains elusive. Here, we showed that meristem genes were differentially expressed in the leaf crenulations of K. pinnata during plantlet development after leaf detachment. The regulatory interactions among these meristem genes are largely conserved in K. pinnata crenulations. Moreover, transgenic antisense (AS) plants with lower expression of these key meristem genes formed significantly fewer plantlets with some morphological defects, suggesting that the meristem genes play an important role in plantlet formation and development. Our research revealed that key meristem genetic pathways were co-opted to the leaf margin to facilitate the unique asexual reproduction mechanism in K. pinnata. This also highlights how evolutionary tinkering invents new structures such as epiphyllous buds and plantlets by rewiring pre-existing genetic pathways.
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spelling pubmed-102009272023-05-23 Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata Jácome-Blásquez, Francisco Kim, Minsung Front Plant Sci Plant Science Several Kalanchoë species reproduce asexually by forming plantlets in the leaf crenulations. Some species produce plantlets incessantly via somatic embryogenesis and organogenesis, whereas others exclusively develop plantlets after leaf detachment, presumably through organogenesis. SHOOT MERISTEMLESS (STM), which mediates SAM functions, appears to be involved in Kalanchoë plantlet formation, suggesting that meristem genes may be essential for plantlet formation. However, the genetic regulatory network for establishing and maintaining plantlet primordia in Kalanchoë remains elusive. Here, we showed that meristem genes were differentially expressed in the leaf crenulations of K. pinnata during plantlet development after leaf detachment. The regulatory interactions among these meristem genes are largely conserved in K. pinnata crenulations. Moreover, transgenic antisense (AS) plants with lower expression of these key meristem genes formed significantly fewer plantlets with some morphological defects, suggesting that the meristem genes play an important role in plantlet formation and development. Our research revealed that key meristem genetic pathways were co-opted to the leaf margin to facilitate the unique asexual reproduction mechanism in K. pinnata. This also highlights how evolutionary tinkering invents new structures such as epiphyllous buds and plantlets by rewiring pre-existing genetic pathways. Frontiers Media S.A. 2023-05-08 /pmc/articles/PMC10200927/ /pubmed/37223821 http://dx.doi.org/10.3389/fpls.2023.1157619 Text en Copyright © 2023 Jácome-Blásquez and Kim 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
Jácome-Blásquez, Francisco
Kim, Minsung
Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title_full Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title_fullStr Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title_full_unstemmed Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title_short Meristem genes are essential for the vegetative reproduction of Kalanchoë pinnata
title_sort meristem genes are essential for the vegetative reproduction of kalanchoë pinnata
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200927/
https://www.ncbi.nlm.nih.gov/pubmed/37223821
http://dx.doi.org/10.3389/fpls.2023.1157619
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