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Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato
Mitogen-activated protein kinase (MAPK) cascades are universal signal transduction modules regulating vegetative and reproductive development of plants. However, the molecular mechanisms of the SlMPK4 gene in tomato pollen and fruit development remain elusive. SlMPK4 is preferentially and highly exp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113226/ https://www.ncbi.nlm.nih.gov/pubmed/35591931 http://dx.doi.org/10.1093/hr/uhac048 |
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author | Wang, Jie Li, Mengzhuo Zhuo, Shibin Liu, Yue Yu, Xiaolin Mukhtar, Sidra Ali, Muhammad Lu, Gang |
author_facet | Wang, Jie Li, Mengzhuo Zhuo, Shibin Liu, Yue Yu, Xiaolin Mukhtar, Sidra Ali, Muhammad Lu, Gang |
author_sort | Wang, Jie |
collection | PubMed |
description | Mitogen-activated protein kinase (MAPK) cascades are universal signal transduction modules regulating vegetative and reproductive development of plants. However, the molecular mechanisms of the SlMPK4 gene in tomato pollen and fruit development remain elusive. SlMPK4 is preferentially and highly expressed in tomato stamens and its mRNA levels increase during early flower development, peaking at the mature pollen stage. Either up- or downregulation of SlMPK4 expression had no significant effect on tomato vegetative growth. However, RNAi-mediated suppression of SlMPK4 caused defects in pollen development, resulting in pollen abortion. The aborted pollen grains were either malformed or collapsed and completely lacked viability, resulting in a predominantly reduced fruit set rate in RNAi lines compared with control and overexpressing transgenic plants. Interestingly, seed development was inhibited in RNAi lines. Moreover, >12% of emasculated RNAi flowers developed seedless fruits without pollination. Anthers can produce typical microspore mother cells as well as uninucleate microspores, according to cytological investigations, while binucleate pollen ceased to produce typical mature pollen. Pollen abortion was further confirmed by transmission electron microscopy analysis at the binucleate stage in RNAi plants. The exine layer in aberrant pollen had a normal structure, while the intine layer appeared thicker. Suppression of SlMPK4 affects the transcript level of genes related to cell wall formation and modification, cell signal transduction, and metabolic and biosynthetic processes. A subset of genes that may be putative substrates of plant MAPKs were also differentially changed in RNAi transgenic flowers. Taken together, these results suggest that SlMPK4 plays a critical role in regulating pollen development and fruit development in tomato plants. |
format | Online Article Text |
id | pubmed-9113226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91132262022-05-18 Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato Wang, Jie Li, Mengzhuo Zhuo, Shibin Liu, Yue Yu, Xiaolin Mukhtar, Sidra Ali, Muhammad Lu, Gang Hortic Res Article Mitogen-activated protein kinase (MAPK) cascades are universal signal transduction modules regulating vegetative and reproductive development of plants. However, the molecular mechanisms of the SlMPK4 gene in tomato pollen and fruit development remain elusive. SlMPK4 is preferentially and highly expressed in tomato stamens and its mRNA levels increase during early flower development, peaking at the mature pollen stage. Either up- or downregulation of SlMPK4 expression had no significant effect on tomato vegetative growth. However, RNAi-mediated suppression of SlMPK4 caused defects in pollen development, resulting in pollen abortion. The aborted pollen grains were either malformed or collapsed and completely lacked viability, resulting in a predominantly reduced fruit set rate in RNAi lines compared with control and overexpressing transgenic plants. Interestingly, seed development was inhibited in RNAi lines. Moreover, >12% of emasculated RNAi flowers developed seedless fruits without pollination. Anthers can produce typical microspore mother cells as well as uninucleate microspores, according to cytological investigations, while binucleate pollen ceased to produce typical mature pollen. Pollen abortion was further confirmed by transmission electron microscopy analysis at the binucleate stage in RNAi plants. The exine layer in aberrant pollen had a normal structure, while the intine layer appeared thicker. Suppression of SlMPK4 affects the transcript level of genes related to cell wall formation and modification, cell signal transduction, and metabolic and biosynthetic processes. A subset of genes that may be putative substrates of plant MAPKs were also differentially changed in RNAi transgenic flowers. Taken together, these results suggest that SlMPK4 plays a critical role in regulating pollen development and fruit development in tomato plants. Oxford University Press 2022-03-14 /pmc/articles/PMC9113226/ /pubmed/35591931 http://dx.doi.org/10.1093/hr/uhac048 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nanjing Agricultural University https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Wang, Jie Li, Mengzhuo Zhuo, Shibin Liu, Yue Yu, Xiaolin Mukhtar, Sidra Ali, Muhammad Lu, Gang Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title | Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title_full | Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title_fullStr | Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title_full_unstemmed | Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title_short | Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
title_sort | mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113226/ https://www.ncbi.nlm.nih.gov/pubmed/35591931 http://dx.doi.org/10.1093/hr/uhac048 |
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