Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1782466052030988288 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5100029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hendelmananat tomatohairymeristemgenesareinvolvedinmeristemmaintenanceandcompoundleafmorphogenesis AT kravchikmichael tomatohairymeristemgenesareinvolvedinmeristemmaintenanceandcompoundleafmorphogenesis AT stavran tomatohairymeristemgenesareinvolvedinmeristemmaintenanceandcompoundleafmorphogenesis AT frankwolfgang tomatohairymeristemgenesareinvolvedinmeristemmaintenanceandcompoundleafmorphogenesis AT arazitzahi tomatohairymeristemgenesareinvolvedinmeristemmaintenanceandcompoundleafmorphogenesis |