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Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation

BACKGROUND: Land plants exhibit a haplodiplontic life cycle, whereby multicellular bodies develop in both the haploid and diploid generations. The early-diverging land plants, known as bryophytes, have a haploid-dominant life cycle, in which a short-lived multicellular body in the diploid generation...

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Autores principales: Yoro, Emiko, Koshimizu, Shizuka, Murata, Takashi, Sakakibara, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521525/
https://www.ncbi.nlm.nih.gov/pubmed/37752568
http://dx.doi.org/10.1186/s13007-023-01077-z
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author Yoro, Emiko
Koshimizu, Shizuka
Murata, Takashi
Sakakibara, Keiko
author_facet Yoro, Emiko
Koshimizu, Shizuka
Murata, Takashi
Sakakibara, Keiko
author_sort Yoro, Emiko
collection PubMed
description BACKGROUND: Land plants exhibit a haplodiplontic life cycle, whereby multicellular bodies develop in both the haploid and diploid generations. The early-diverging land plants, known as bryophytes, have a haploid-dominant life cycle, in which a short-lived multicellular body in the diploid generation, known as the sporophyte, develops on the maternal haploid gametophyte tissues. The moss Physcomitrium (Physcomitrella) patens has become one of the most powerful model systems in evolutionary plant developmental studies. To induce diploid sporophytes of P. patens, several protocols are implemented. One of the conventional approaches is to grow approximately one-month-old gametophores for another month on Jiffy-7 pellets made from the peat moss that is difficult to fully sterilize. A more efficient method to obtain all tissues throughout the life cycle should accelerate studies of P. patens. RESULTS: Here, we investigated the effect of nitrogen conditions on the growth and development of P. patens. We provide an improved protocol for the sporophyte induction of P. patens using a BCD-based solid culture medium without Jiffy-7 pellets, based on the finding that the formation of gametangia and subsequent sporophytes is promoted by nitrogen-free growth conditions. The protocol consists of two steps; first, culture the protonemata and gametophores on nitrogen-rich medium under continuous light at 25 °C, and then transfer the gametophores onto nitrogen-free medium under short-day and at 15 °C for sporophyte induction. The protocol enables to shorten the induction period and reduce the culture space. CONCLUSIONS: Our more efficient and shortened protocol for inducing the formation of sporophytes will contribute to future studies into the fertilization or the diploid sporophyte generation of P. patens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-023-01077-z.
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spelling pubmed-105215252023-09-27 Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation Yoro, Emiko Koshimizu, Shizuka Murata, Takashi Sakakibara, Keiko Plant Methods Methodology BACKGROUND: Land plants exhibit a haplodiplontic life cycle, whereby multicellular bodies develop in both the haploid and diploid generations. The early-diverging land plants, known as bryophytes, have a haploid-dominant life cycle, in which a short-lived multicellular body in the diploid generation, known as the sporophyte, develops on the maternal haploid gametophyte tissues. The moss Physcomitrium (Physcomitrella) patens has become one of the most powerful model systems in evolutionary plant developmental studies. To induce diploid sporophytes of P. patens, several protocols are implemented. One of the conventional approaches is to grow approximately one-month-old gametophores for another month on Jiffy-7 pellets made from the peat moss that is difficult to fully sterilize. A more efficient method to obtain all tissues throughout the life cycle should accelerate studies of P. patens. RESULTS: Here, we investigated the effect of nitrogen conditions on the growth and development of P. patens. We provide an improved protocol for the sporophyte induction of P. patens using a BCD-based solid culture medium without Jiffy-7 pellets, based on the finding that the formation of gametangia and subsequent sporophytes is promoted by nitrogen-free growth conditions. The protocol consists of two steps; first, culture the protonemata and gametophores on nitrogen-rich medium under continuous light at 25 °C, and then transfer the gametophores onto nitrogen-free medium under short-day and at 15 °C for sporophyte induction. The protocol enables to shorten the induction period and reduce the culture space. CONCLUSIONS: Our more efficient and shortened protocol for inducing the formation of sporophytes will contribute to future studies into the fertilization or the diploid sporophyte generation of P. patens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-023-01077-z. BioMed Central 2023-09-26 /pmc/articles/PMC10521525/ /pubmed/37752568 http://dx.doi.org/10.1186/s13007-023-01077-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (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
Yoro, Emiko
Koshimizu, Shizuka
Murata, Takashi
Sakakibara, Keiko
Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title_full Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title_fullStr Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title_full_unstemmed Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title_short Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
title_sort protocol: an improved method for inducing sporophyte generation in the model moss physcomitrium patens under nitrogen starvation
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521525/
https://www.ncbi.nlm.nih.gov/pubmed/37752568
http://dx.doi.org/10.1186/s13007-023-01077-z
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