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Polar auxin transport modulates early leaf flattening
The flattened leaf form is an important adaptation for efficient photosynthesis, and the developmental process of flattened leaves has been intensively studied. Classic microsurgery studies in potato and tomato suggest that the shoot apical meristem (SAM) communicates with the leaf primordia to prom...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897438/ https://www.ncbi.nlm.nih.gov/pubmed/36469773 http://dx.doi.org/10.1073/pnas.2215569119 |
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author | Wang, Qingqing Marconi, Marco Guan, Chunmei Wabnik, Krzysztof Jiao, Yuling |
author_facet | Wang, Qingqing Marconi, Marco Guan, Chunmei Wabnik, Krzysztof Jiao, Yuling |
author_sort | Wang, Qingqing |
collection | PubMed |
description | The flattened leaf form is an important adaptation for efficient photosynthesis, and the developmental process of flattened leaves has been intensively studied. Classic microsurgery studies in potato and tomato suggest that the shoot apical meristem (SAM) communicates with the leaf primordia to promote leaf blade formation. More recently, it was found that polar auxin transport (PAT) could mediate this communication. However, it is unclear how the expression of leaf patterning genes is tailored by PAT routes originating from SAM. By combining experimental observations and computer model simulations, we show that microsurgical incisions and local inhibition of PAT in tomato interfere with auxin transport toward the leaf margins, reducing auxin response levels and altering the leaf blade shape. Importantly, oval auxin responses result in the bipolar expression of SlLAM1 that determines leaf blade formation. Furthermore, wounding caused by incisions promotes degradation of SlREV, a known regulator of leaf polarity. Additionally, computer simulations suggest that local auxin biosynthesis in early leaf primordia could remove necessity for external auxin supply originating from SAM, potentially explaining differences between species. Together, our findings establish how PAT near emerging leaf primordia determines spatial auxin patterning and refines SlLAM1 expression in the leaf margins to guide leaf flattening. |
format | Online Article Text |
id | pubmed-9897438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-98974382023-02-04 Polar auxin transport modulates early leaf flattening Wang, Qingqing Marconi, Marco Guan, Chunmei Wabnik, Krzysztof Jiao, Yuling Proc Natl Acad Sci U S A Biological Sciences The flattened leaf form is an important adaptation for efficient photosynthesis, and the developmental process of flattened leaves has been intensively studied. Classic microsurgery studies in potato and tomato suggest that the shoot apical meristem (SAM) communicates with the leaf primordia to promote leaf blade formation. More recently, it was found that polar auxin transport (PAT) could mediate this communication. However, it is unclear how the expression of leaf patterning genes is tailored by PAT routes originating from SAM. By combining experimental observations and computer model simulations, we show that microsurgical incisions and local inhibition of PAT in tomato interfere with auxin transport toward the leaf margins, reducing auxin response levels and altering the leaf blade shape. Importantly, oval auxin responses result in the bipolar expression of SlLAM1 that determines leaf blade formation. Furthermore, wounding caused by incisions promotes degradation of SlREV, a known regulator of leaf polarity. Additionally, computer simulations suggest that local auxin biosynthesis in early leaf primordia could remove necessity for external auxin supply originating from SAM, potentially explaining differences between species. Together, our findings establish how PAT near emerging leaf primordia determines spatial auxin patterning and refines SlLAM1 expression in the leaf margins to guide leaf flattening. National Academy of Sciences 2022-12-05 2022-12-13 /pmc/articles/PMC9897438/ /pubmed/36469773 http://dx.doi.org/10.1073/pnas.2215569119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Wang, Qingqing Marconi, Marco Guan, Chunmei Wabnik, Krzysztof Jiao, Yuling Polar auxin transport modulates early leaf flattening |
title | Polar auxin transport modulates early leaf flattening |
title_full | Polar auxin transport modulates early leaf flattening |
title_fullStr | Polar auxin transport modulates early leaf flattening |
title_full_unstemmed | Polar auxin transport modulates early leaf flattening |
title_short | Polar auxin transport modulates early leaf flattening |
title_sort | polar auxin transport modulates early leaf flattening |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897438/ https://www.ncbi.nlm.nih.gov/pubmed/36469773 http://dx.doi.org/10.1073/pnas.2215569119 |
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