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Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis

The HAIRY MERISTEM (HAM) genes function in meristem maintenance but play minor roles in the morphogenesis of a simple leaf that is determinate. Here, we functionally analyzed HAM genes in tomato and uncovered their involvement in compound leaf morphogenesis. Tomato encodes three HAM homologs, of whi...

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Autores principales: Hendelman, Anat, Kravchik, Michael, Stav, Ran, Frank, Wolfgang, Arazi, Tzahi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100029/
https://www.ncbi.nlm.nih.gov/pubmed/27811085
http://dx.doi.org/10.1093/jxb/erw388
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author Hendelman, Anat
Kravchik, Michael
Stav, Ran
Frank, Wolfgang
Arazi, Tzahi
author_facet Hendelman, Anat
Kravchik, Michael
Stav, Ran
Frank, Wolfgang
Arazi, Tzahi
author_sort Hendelman, Anat
collection PubMed
description The HAIRY MERISTEM (HAM) genes function in meristem maintenance but play minor roles in the morphogenesis of a simple leaf that is determinate. Here, we functionally analyzed HAM genes in tomato and uncovered their involvement in compound leaf morphogenesis. Tomato encodes three HAM homologs, of which SlHAM and SlHAM2 (SlHAMs) are guided for cleavage by microRNA171 and are abundant in the shoot and floral meristems as well as in the compound leaf primordia. We found that SlHAMs silencing led to overproliferation of cells in the periphery of the meristems where SlHAM is localized. As in meristems, leaf-specific silencing of SlHAMs provoked overproliferation of meristematic cells in the organogenic compound leaf rachis. We further demonstrate that the meristematic cell overproliferation in both meristems and leaves was in part due to the misexpression of the stem cell regulator WUSCHEL, previously shown to be induced by cytokinin. Strikingly, reduction of cytokinin levels in SlHAMs-silenced leaves completely suppressed the overproliferation phenotype, suggesting a regulatory link between SlHAMs and cytokinin, a key hormone found to promote indeterminacy in meristems and leaves. Taken together, our data provide evidence that in addition to their conserved function in meristem maintenance, SlHAMs are also required for the proper morphogenesis of the compound leaf.
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spelling pubmed-51000292016-11-10 Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis Hendelman, Anat Kravchik, Michael Stav, Ran Frank, Wolfgang Arazi, Tzahi J Exp Bot Research Paper The HAIRY MERISTEM (HAM) genes function in meristem maintenance but play minor roles in the morphogenesis of a simple leaf that is determinate. Here, we functionally analyzed HAM genes in tomato and uncovered their involvement in compound leaf morphogenesis. Tomato encodes three HAM homologs, of which SlHAM and SlHAM2 (SlHAMs) are guided for cleavage by microRNA171 and are abundant in the shoot and floral meristems as well as in the compound leaf primordia. We found that SlHAMs silencing led to overproliferation of cells in the periphery of the meristems where SlHAM is localized. As in meristems, leaf-specific silencing of SlHAMs provoked overproliferation of meristematic cells in the organogenic compound leaf rachis. We further demonstrate that the meristematic cell overproliferation in both meristems and leaves was in part due to the misexpression of the stem cell regulator WUSCHEL, previously shown to be induced by cytokinin. Strikingly, reduction of cytokinin levels in SlHAMs-silenced leaves completely suppressed the overproliferation phenotype, suggesting a regulatory link between SlHAMs and cytokinin, a key hormone found to promote indeterminacy in meristems and leaves. Taken together, our data provide evidence that in addition to their conserved function in meristem maintenance, SlHAMs are also required for the proper morphogenesis of the compound leaf. Oxford University Press 2016-11 2016-11-03 /pmc/articles/PMC5100029/ /pubmed/27811085 http://dx.doi.org/10.1093/jxb/erw388 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Hendelman, Anat
Kravchik, Michael
Stav, Ran
Frank, Wolfgang
Arazi, Tzahi
Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title_full Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title_fullStr Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title_full_unstemmed Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title_short Tomato HAIRY MERISTEM genes are involved in meristem maintenance and compound leaf morphogenesis
title_sort tomato hairy meristem genes are involved in meristem maintenance and compound leaf morphogenesis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100029/
https://www.ncbi.nlm.nih.gov/pubmed/27811085
http://dx.doi.org/10.1093/jxb/erw388
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