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BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves

Axis formation is a fundamental issue in developmental biology. Axis formation and patterning in plant leaves is crucial for morphology and crop productivity. Here, we reveal the basis of proximal-distal patterning in rice leaves, which consist of a proximal sheath, a distal blade, and boundary orga...

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Autores principales: Toriba, Taiyo, Tokunaga, Hiroki, Shiga, Toshihide, Nie, Fanyu, Naramoto, Satoshi, Honda, Eriko, Tanaka, Keisuke, Taji, Teruaki, Itoh, Jun-Ichi, Kyozuka, Junko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365560/
https://www.ncbi.nlm.nih.gov/pubmed/30728357
http://dx.doi.org/10.1038/s41467-019-08479-5
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author Toriba, Taiyo
Tokunaga, Hiroki
Shiga, Toshihide
Nie, Fanyu
Naramoto, Satoshi
Honda, Eriko
Tanaka, Keisuke
Taji, Teruaki
Itoh, Jun-Ichi
Kyozuka, Junko
author_facet Toriba, Taiyo
Tokunaga, Hiroki
Shiga, Toshihide
Nie, Fanyu
Naramoto, Satoshi
Honda, Eriko
Tanaka, Keisuke
Taji, Teruaki
Itoh, Jun-Ichi
Kyozuka, Junko
author_sort Toriba, Taiyo
collection PubMed
description Axis formation is a fundamental issue in developmental biology. Axis formation and patterning in plant leaves is crucial for morphology and crop productivity. Here, we reveal the basis of proximal-distal patterning in rice leaves, which consist of a proximal sheath, a distal blade, and boundary organs formed between these two regions. Analysis of the three rice homologs of the Arabidopsis BLADE-ON-PETIOLE1 (BOP1) gene indicates that OsBOPs activate proximal sheath differentiation and suppress distal blade differentiation. Temporal expression changes of OsBOPs are responsible for the developmental changes in the sheath:blade ratio. We further identify that the change in the sheath:blade ratio during the juvenile phase is controlled by the miR156/SPL pathway, which modifies the level and pattern of expression of OsBOPs. OsBOPs are also essential for differentiation of the boundary organs. We propose that OsBOPs, the main regulators of proximal-distal patterning, control temporal changes in the sheath:blade ratio of rice leaves.
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spelling pubmed-63655602019-02-08 BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves Toriba, Taiyo Tokunaga, Hiroki Shiga, Toshihide Nie, Fanyu Naramoto, Satoshi Honda, Eriko Tanaka, Keisuke Taji, Teruaki Itoh, Jun-Ichi Kyozuka, Junko Nat Commun Article Axis formation is a fundamental issue in developmental biology. Axis formation and patterning in plant leaves is crucial for morphology and crop productivity. Here, we reveal the basis of proximal-distal patterning in rice leaves, which consist of a proximal sheath, a distal blade, and boundary organs formed between these two regions. Analysis of the three rice homologs of the Arabidopsis BLADE-ON-PETIOLE1 (BOP1) gene indicates that OsBOPs activate proximal sheath differentiation and suppress distal blade differentiation. Temporal expression changes of OsBOPs are responsible for the developmental changes in the sheath:blade ratio. We further identify that the change in the sheath:blade ratio during the juvenile phase is controlled by the miR156/SPL pathway, which modifies the level and pattern of expression of OsBOPs. OsBOPs are also essential for differentiation of the boundary organs. We propose that OsBOPs, the main regulators of proximal-distal patterning, control temporal changes in the sheath:blade ratio of rice leaves. Nature Publishing Group UK 2019-02-06 /pmc/articles/PMC6365560/ /pubmed/30728357 http://dx.doi.org/10.1038/s41467-019-08479-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Toriba, Taiyo
Tokunaga, Hiroki
Shiga, Toshihide
Nie, Fanyu
Naramoto, Satoshi
Honda, Eriko
Tanaka, Keisuke
Taji, Teruaki
Itoh, Jun-Ichi
Kyozuka, Junko
BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title_full BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title_fullStr BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title_full_unstemmed BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title_short BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
title_sort blade-on-petiole genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365560/
https://www.ncbi.nlm.nih.gov/pubmed/30728357
http://dx.doi.org/10.1038/s41467-019-08479-5
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