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Using RNA-seq to characterize pollen–stigma interactions for pollination studies

Insects are essential for the reproduction of pollinator-dependent crops and contribute to the pollination of 87% of wild plants and 75% of the world’s food crops. Understanding pollen flow dynamics between plants and pollinators is thus essential to manage and conserve wild plants and ensure yields...

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Autores principales: Lobaton, Juan, Andrew, Rose, Duitama, Jorge, Kirkland, Lindsey, Macfadyen, Sarina, Rader, Romina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988043/
https://www.ncbi.nlm.nih.gov/pubmed/33758263
http://dx.doi.org/10.1038/s41598-021-85887-y
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author Lobaton, Juan
Andrew, Rose
Duitama, Jorge
Kirkland, Lindsey
Macfadyen, Sarina
Rader, Romina
author_facet Lobaton, Juan
Andrew, Rose
Duitama, Jorge
Kirkland, Lindsey
Macfadyen, Sarina
Rader, Romina
author_sort Lobaton, Juan
collection PubMed
description Insects are essential for the reproduction of pollinator-dependent crops and contribute to the pollination of 87% of wild plants and 75% of the world’s food crops. Understanding pollen flow dynamics between plants and pollinators is thus essential to manage and conserve wild plants and ensure yields are maximized in food crops. However, the determination of pollen transfer in the field is complex and laborious. We developed a field experiment in a pollinator-dependent crop and used high throughput RNA sequencing (RNA-seq) to quantify pollen flow by measuring changes in gene expression between pollination treatments across different apple (Malus domestica Borkh.) cultivars. We tested three potential molecular indicators of successful pollination and validated these results with field data by observing single and multiple visits by honey bees (Apis mellifera) to apple flowers and measured fruit set in a commercial apple orchard. The first indicator of successful outcrossing was revealed via differential gene expression in the cross-pollination treatments after 6 h. The second indicator of successful outcrossing was revealed by the expression of specific genes related to pollen tube formation and defense response at three different time intervals in the stigma and the style following cross-pollination (i.e. after 6, 24, and 48 h). Finally, genotyping variants specific to donor pollen could be detected in cross-pollination treatments, providing a third indicator of successful outcrossing. Field data indicated that one or five flower visits by honey bees were insufficient and at least 10 honey bee flower visits were required to achieve a 25% probability of fruit set under orchard conditions. By combining the genotyping data, the differential expression analysis, and the traditional fruit set field experiments, it was possible to evaluate the pollination effectiveness of honey bee visits under orchards conditions. This is the first time that pollen-stigma-style mRNA expression analysis has been conducted after a pollinator visit (honey bee) to a plant (in vivo apple flowers). This study provides evidence that mRNA sequencing can be used to address complex questions related to stigma–pollen interactions over time in pollination ecology.
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spelling pubmed-79880432021-03-25 Using RNA-seq to characterize pollen–stigma interactions for pollination studies Lobaton, Juan Andrew, Rose Duitama, Jorge Kirkland, Lindsey Macfadyen, Sarina Rader, Romina Sci Rep Article Insects are essential for the reproduction of pollinator-dependent crops and contribute to the pollination of 87% of wild plants and 75% of the world’s food crops. Understanding pollen flow dynamics between plants and pollinators is thus essential to manage and conserve wild plants and ensure yields are maximized in food crops. However, the determination of pollen transfer in the field is complex and laborious. We developed a field experiment in a pollinator-dependent crop and used high throughput RNA sequencing (RNA-seq) to quantify pollen flow by measuring changes in gene expression between pollination treatments across different apple (Malus domestica Borkh.) cultivars. We tested three potential molecular indicators of successful pollination and validated these results with field data by observing single and multiple visits by honey bees (Apis mellifera) to apple flowers and measured fruit set in a commercial apple orchard. The first indicator of successful outcrossing was revealed via differential gene expression in the cross-pollination treatments after 6 h. The second indicator of successful outcrossing was revealed by the expression of specific genes related to pollen tube formation and defense response at three different time intervals in the stigma and the style following cross-pollination (i.e. after 6, 24, and 48 h). Finally, genotyping variants specific to donor pollen could be detected in cross-pollination treatments, providing a third indicator of successful outcrossing. Field data indicated that one or five flower visits by honey bees were insufficient and at least 10 honey bee flower visits were required to achieve a 25% probability of fruit set under orchard conditions. By combining the genotyping data, the differential expression analysis, and the traditional fruit set field experiments, it was possible to evaluate the pollination effectiveness of honey bee visits under orchards conditions. This is the first time that pollen-stigma-style mRNA expression analysis has been conducted after a pollinator visit (honey bee) to a plant (in vivo apple flowers). This study provides evidence that mRNA sequencing can be used to address complex questions related to stigma–pollen interactions over time in pollination ecology. Nature Publishing Group UK 2021-03-23 /pmc/articles/PMC7988043/ /pubmed/33758263 http://dx.doi.org/10.1038/s41598-021-85887-y Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lobaton, Juan
Andrew, Rose
Duitama, Jorge
Kirkland, Lindsey
Macfadyen, Sarina
Rader, Romina
Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title_full Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title_fullStr Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title_full_unstemmed Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title_short Using RNA-seq to characterize pollen–stigma interactions for pollination studies
title_sort using rna-seq to characterize pollen–stigma interactions for pollination studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988043/
https://www.ncbi.nlm.nih.gov/pubmed/33758263
http://dx.doi.org/10.1038/s41598-021-85887-y
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