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A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations

BACKGROUND: Post-embryonic growth of land plants originates from meristems. Genetic networks in meristems maintain the stem cells and direct acquisition of cell fates. WUSCHEL-RELATED HOMEOBOX (WOX) transcription factors involved in meristem networks have only been functionally characterized in two...

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Autores principales: Youngstrom, Christopher E., Geadelmann, Lander F., Irish, Erin E., Cheng, Chi-Lien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788082/
https://www.ncbi.nlm.nih.gov/pubmed/31601197
http://dx.doi.org/10.1186/s12870-019-1991-8
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author Youngstrom, Christopher E.
Geadelmann, Lander F.
Irish, Erin E.
Cheng, Chi-Lien
author_facet Youngstrom, Christopher E.
Geadelmann, Lander F.
Irish, Erin E.
Cheng, Chi-Lien
author_sort Youngstrom, Christopher E.
collection PubMed
description BACKGROUND: Post-embryonic growth of land plants originates from meristems. Genetic networks in meristems maintain the stem cells and direct acquisition of cell fates. WUSCHEL-RELATED HOMEOBOX (WOX) transcription factors involved in meristem networks have only been functionally characterized in two evolutionarily distant taxa, mosses and seed plants. This report characterizes a WOX gene in a fern, which is located phylogenetically between the two taxa. RESULTS: CrWOXB transcripts were detected in proliferating tissues, including gametophyte and sporophyte meristems of Ceratopteris richardii. In addition, CrWOXB is expressed in archegonia but not the antheridia of gametophytes. Suppression of CrWOXB expression in wild-type RN3 plants by RNAi produced abnormal morphologies of gametophytes and sporophytes. The gametophytes of RNAi lines produced fewer cells, and fewer female gametes compared to wild-type. In the sporophyte generation, RNAi lines produced fewer leaves, pinnae, roots and lateral roots compared to wild-type sporophytes. CONCLUSIONS: Our results suggest that CrWOXB functions to promote cell divisions and organ development in the gametophyte and sporophyte generations, respectively. CrWOXB is the first intermediate-clade WOX gene shown to function in both generations in land plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1991-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-67880822019-10-18 A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations Youngstrom, Christopher E. Geadelmann, Lander F. Irish, Erin E. Cheng, Chi-Lien BMC Plant Biol Research Article BACKGROUND: Post-embryonic growth of land plants originates from meristems. Genetic networks in meristems maintain the stem cells and direct acquisition of cell fates. WUSCHEL-RELATED HOMEOBOX (WOX) transcription factors involved in meristem networks have only been functionally characterized in two evolutionarily distant taxa, mosses and seed plants. This report characterizes a WOX gene in a fern, which is located phylogenetically between the two taxa. RESULTS: CrWOXB transcripts were detected in proliferating tissues, including gametophyte and sporophyte meristems of Ceratopteris richardii. In addition, CrWOXB is expressed in archegonia but not the antheridia of gametophytes. Suppression of CrWOXB expression in wild-type RN3 plants by RNAi produced abnormal morphologies of gametophytes and sporophytes. The gametophytes of RNAi lines produced fewer cells, and fewer female gametes compared to wild-type. In the sporophyte generation, RNAi lines produced fewer leaves, pinnae, roots and lateral roots compared to wild-type sporophytes. CONCLUSIONS: Our results suggest that CrWOXB functions to promote cell divisions and organ development in the gametophyte and sporophyte generations, respectively. CrWOXB is the first intermediate-clade WOX gene shown to function in both generations in land plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1991-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-10-11 /pmc/articles/PMC6788082/ /pubmed/31601197 http://dx.doi.org/10.1186/s12870-019-1991-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Youngstrom, Christopher E.
Geadelmann, Lander F.
Irish, Erin E.
Cheng, Chi-Lien
A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title_full A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title_fullStr A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title_full_unstemmed A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title_short A fern WUSCHEL-RELATED HOMEOBOX gene functions in both gametophyte and sporophyte generations
title_sort fern wuschel-related homeobox gene functions in both gametophyte and sporophyte generations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788082/
https://www.ncbi.nlm.nih.gov/pubmed/31601197
http://dx.doi.org/10.1186/s12870-019-1991-8
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