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A protocol for Chenopodium quinoa pollen germination
BACKGROUND: Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118578/ https://www.ncbi.nlm.nih.gov/pubmed/35585546 http://dx.doi.org/10.1186/s13007-022-00900-3 |
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author | Castillo, S. Elizabeth Tovar, Jose C. Shamin, Anastasia Gutirerrez, Jorge Pearson, Paige Gehan, Malia A. |
author_facet | Castillo, S. Elizabeth Tovar, Jose C. Shamin, Anastasia Gutirerrez, Jorge Pearson, Paige Gehan, Malia A. |
author_sort | Castillo, S. Elizabeth |
collection | PubMed |
description | BACKGROUND: Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains is to estimate pollen viability through in vitro germination. Here we report a method for in vitro quinoa pollen germination that could be used to understand the impact of various stresses on quinoa fertility and therefore seed yield or to identify male-sterile lines for breeding. RESULTS: A semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community. Pollen collected on day 4 after first anthesis at zeitgeber time 5 was optimum for pollen germination with an average germination of 68% for accession QQ74 (PI 614886). The optimal length of pollen incubation was found to be 48 h, because it maximizes germination rates while minimizing contamination. The pollen germination medium’s pH, boric acid, and sucrose concentrations were optimized. The highest germination rates were obtained with 16% sucrose, 0.03% boric acid, 0.007% calcium nitrate, and pH 5.5. This medium was tested on quinoa accessions QQ74, and cherry vanilla with 68%, and 64% germination efficiencies, respectively. CONCLUSIONS: We provide an in vitro pollen germination method for quinoa with average germination rates of 64 and 68% on the two accessions tested. This method is a valuable tool to estimate pollen viability in quinoa, and to test how stress affects quinoa fertility. We also developed an image analysis tool to semi-automate the process of counting germinating pollen. Quinoa produces many new flowers during most of its panicle development period, leading to significant variation in pollen maturity and viability between different flowers of the same panicle. Therefore, collecting pollen at 4 days after first anthesis is very important to collect more uniformly developed pollen and to obtain high germination rates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00900-3. |
format | Online Article Text |
id | pubmed-9118578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91185782022-05-20 A protocol for Chenopodium quinoa pollen germination Castillo, S. Elizabeth Tovar, Jose C. Shamin, Anastasia Gutirerrez, Jorge Pearson, Paige Gehan, Malia A. Plant Methods Methodology BACKGROUND: Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains is to estimate pollen viability through in vitro germination. Here we report a method for in vitro quinoa pollen germination that could be used to understand the impact of various stresses on quinoa fertility and therefore seed yield or to identify male-sterile lines for breeding. RESULTS: A semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community. Pollen collected on day 4 after first anthesis at zeitgeber time 5 was optimum for pollen germination with an average germination of 68% for accession QQ74 (PI 614886). The optimal length of pollen incubation was found to be 48 h, because it maximizes germination rates while minimizing contamination. The pollen germination medium’s pH, boric acid, and sucrose concentrations were optimized. The highest germination rates were obtained with 16% sucrose, 0.03% boric acid, 0.007% calcium nitrate, and pH 5.5. This medium was tested on quinoa accessions QQ74, and cherry vanilla with 68%, and 64% germination efficiencies, respectively. CONCLUSIONS: We provide an in vitro pollen germination method for quinoa with average germination rates of 64 and 68% on the two accessions tested. This method is a valuable tool to estimate pollen viability in quinoa, and to test how stress affects quinoa fertility. We also developed an image analysis tool to semi-automate the process of counting germinating pollen. Quinoa produces many new flowers during most of its panicle development period, leading to significant variation in pollen maturity and viability between different flowers of the same panicle. Therefore, collecting pollen at 4 days after first anthesis is very important to collect more uniformly developed pollen and to obtain high germination rates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00900-3. BioMed Central 2022-05-18 /pmc/articles/PMC9118578/ /pubmed/35585546 http://dx.doi.org/10.1186/s13007-022-00900-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Castillo, S. Elizabeth Tovar, Jose C. Shamin, Anastasia Gutirerrez, Jorge Pearson, Paige Gehan, Malia A. A protocol for Chenopodium quinoa pollen germination |
title | A protocol for Chenopodium quinoa pollen germination |
title_full | A protocol for Chenopodium quinoa pollen germination |
title_fullStr | A protocol for Chenopodium quinoa pollen germination |
title_full_unstemmed | A protocol for Chenopodium quinoa pollen germination |
title_short | A protocol for Chenopodium quinoa pollen germination |
title_sort | protocol for chenopodium quinoa pollen germination |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118578/ https://www.ncbi.nlm.nih.gov/pubmed/35585546 http://dx.doi.org/10.1186/s13007-022-00900-3 |
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