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A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays

Murashige-Skoog medium solutions have been used in a variety of plant plate growth assays, yet most research uses Arabidopsis thaliana as the study organism. For larger seeds such as maize (Zea mays), most protocols employ a paper towel roll method for experiments, which often involves wrapping maiz...

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Detalles Bibliográficos
Autores principales: Roberts, Jason T., McCubbin, Tyler J., Braun, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bio-Protocol 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603264/
https://www.ncbi.nlm.nih.gov/pubmed/37900110
http://dx.doi.org/10.21769/BioProtoc.4858
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author Roberts, Jason T.
McCubbin, Tyler J.
Braun, David M.
author_facet Roberts, Jason T.
McCubbin, Tyler J.
Braun, David M.
author_sort Roberts, Jason T.
collection PubMed
description Murashige-Skoog medium solutions have been used in a variety of plant plate growth assays, yet most research uses Arabidopsis thaliana as the study organism. For larger seeds such as maize (Zea mays), most protocols employ a paper towel roll method for experiments, which often involves wrapping maize seedlings in wet, sterile germination paper. What the paper towel roll method lacks, however, is the ability to image the roots over time without risk of contamination. Here, we describe a sterile plate growth assay that contains Murashige-Skoog medium to grow seedlings starting two days after germination. This protocol uses a section of a paper towel roll method to achieve uniform germination of maize seedlings, which are sterilely transferred onto large acrylic plates for the duration of the experiment. The media can undergo modification to include an assortment of plant hormones, exogenous sugars, and other chemicals. The acrylic plates allow researchers to freely image the plate without disturbing the seedlings and control the environment in which the seedlings are grown, such as modifications in temperature and light. Additionally, the protocol is widely adaptable for use with other cereal crops. Key features • Builds upon plate growth methods routinely used for Arabidopsis seedlings but that are inadequate for maize. • Real-time photographic analysis of seedlings up to two weeks following germination. • Allows for testing of various growth conditions involving an assortment of additives and/or modification of environmental conditions. • Samples are able to be collected for genotype screening.
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spelling pubmed-106032642023-10-28 A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays Roberts, Jason T. McCubbin, Tyler J. Braun, David M. Bio Protoc Methods Article Murashige-Skoog medium solutions have been used in a variety of plant plate growth assays, yet most research uses Arabidopsis thaliana as the study organism. For larger seeds such as maize (Zea mays), most protocols employ a paper towel roll method for experiments, which often involves wrapping maize seedlings in wet, sterile germination paper. What the paper towel roll method lacks, however, is the ability to image the roots over time without risk of contamination. Here, we describe a sterile plate growth assay that contains Murashige-Skoog medium to grow seedlings starting two days after germination. This protocol uses a section of a paper towel roll method to achieve uniform germination of maize seedlings, which are sterilely transferred onto large acrylic plates for the duration of the experiment. The media can undergo modification to include an assortment of plant hormones, exogenous sugars, and other chemicals. The acrylic plates allow researchers to freely image the plate without disturbing the seedlings and control the environment in which the seedlings are grown, such as modifications in temperature and light. Additionally, the protocol is widely adaptable for use with other cereal crops. Key features • Builds upon plate growth methods routinely used for Arabidopsis seedlings but that are inadequate for maize. • Real-time photographic analysis of seedlings up to two weeks following germination. • Allows for testing of various growth conditions involving an assortment of additives and/or modification of environmental conditions. • Samples are able to be collected for genotype screening. Bio-Protocol 2023-10-20 /pmc/articles/PMC10603264/ /pubmed/37900110 http://dx.doi.org/10.21769/BioProtoc.4858 Text en ©Copyright : © 2023 The Authors; This is an open access article under the CC BY-NC license https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Methods Article
Roberts, Jason T.
McCubbin, Tyler J.
Braun, David M.
A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title_full A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title_fullStr A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title_full_unstemmed A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title_short A Plate Growth Assay to Quantify Embryonic Root Development of Zea mays
title_sort plate growth assay to quantify embryonic root development of zea mays
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603264/
https://www.ncbi.nlm.nih.gov/pubmed/37900110
http://dx.doi.org/10.21769/BioProtoc.4858
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