Cargando…
Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants
KNOX and BELL transcription factors regulate distinct steps of diploid development in plants. In the green alga Chlamydomonas reinhardtii, KNOX and BELL proteins are inherited by gametes of the opposite mating types and heterodimerize in zygotes to activate diploid development. By contrast, in land...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478417/ https://www.ncbi.nlm.nih.gov/pubmed/34579806 http://dx.doi.org/10.7554/eLife.57090 |
_version_ | 1784576052657389568 |
---|---|
author | Hisanaga, Tetsuya Fujimoto, Shota Cui, Yihui Sato, Katsutoshi Sano, Ryosuke Yamaoka, Shohei Kohchi, Takayuki Berger, Frédéric Nakajima, Keiji |
author_facet | Hisanaga, Tetsuya Fujimoto, Shota Cui, Yihui Sato, Katsutoshi Sano, Ryosuke Yamaoka, Shohei Kohchi, Takayuki Berger, Frédéric Nakajima, Keiji |
author_sort | Hisanaga, Tetsuya |
collection | PubMed |
description | KNOX and BELL transcription factors regulate distinct steps of diploid development in plants. In the green alga Chlamydomonas reinhardtii, KNOX and BELL proteins are inherited by gametes of the opposite mating types and heterodimerize in zygotes to activate diploid development. By contrast, in land plants such as Physcomitrium patens and Arabidopsis thaliana, KNOX and BELL proteins function in sporophyte and spore formation, meristem maintenance and organogenesis during the later stages of diploid development. However, whether the contrasting functions of KNOX and BELL were acquired independently in algae and land plants is currently unknown. Here, we show that in the basal land plant species Marchantia polymorpha, gamete-expressed KNOX and BELL are required to initiate zygotic development by promoting nuclear fusion in a manner strikingly similar to that in C. reinhardtii. Our results indicate that zygote activation is the ancestral role of KNOX/BELL transcription factors, which shifted toward meristem maintenance as land plants evolved. |
format | Online Article Text |
id | pubmed-8478417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84784172021-09-30 Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants Hisanaga, Tetsuya Fujimoto, Shota Cui, Yihui Sato, Katsutoshi Sano, Ryosuke Yamaoka, Shohei Kohchi, Takayuki Berger, Frédéric Nakajima, Keiji eLife Developmental Biology KNOX and BELL transcription factors regulate distinct steps of diploid development in plants. In the green alga Chlamydomonas reinhardtii, KNOX and BELL proteins are inherited by gametes of the opposite mating types and heterodimerize in zygotes to activate diploid development. By contrast, in land plants such as Physcomitrium patens and Arabidopsis thaliana, KNOX and BELL proteins function in sporophyte and spore formation, meristem maintenance and organogenesis during the later stages of diploid development. However, whether the contrasting functions of KNOX and BELL were acquired independently in algae and land plants is currently unknown. Here, we show that in the basal land plant species Marchantia polymorpha, gamete-expressed KNOX and BELL are required to initiate zygotic development by promoting nuclear fusion in a manner strikingly similar to that in C. reinhardtii. Our results indicate that zygote activation is the ancestral role of KNOX/BELL transcription factors, which shifted toward meristem maintenance as land plants evolved. eLife Sciences Publications, Ltd 2021-09-28 /pmc/articles/PMC8478417/ /pubmed/34579806 http://dx.doi.org/10.7554/eLife.57090 Text en © 2021, Hisanaga et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Hisanaga, Tetsuya Fujimoto, Shota Cui, Yihui Sato, Katsutoshi Sano, Ryosuke Yamaoka, Shohei Kohchi, Takayuki Berger, Frédéric Nakajima, Keiji Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title | Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title_full | Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title_fullStr | Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title_full_unstemmed | Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title_short | Deep evolutionary origin of gamete-directed zygote activation by KNOX/BELL transcription factors in green plants |
title_sort | deep evolutionary origin of gamete-directed zygote activation by knox/bell transcription factors in green plants |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478417/ https://www.ncbi.nlm.nih.gov/pubmed/34579806 http://dx.doi.org/10.7554/eLife.57090 |
work_keys_str_mv | AT hisanagatetsuya deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT fujimotoshota deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT cuiyihui deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT satokatsutoshi deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT sanoryosuke deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT yamaokashohei deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT kohchitakayuki deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT bergerfrederic deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants AT nakajimakeiji deepevolutionaryoriginofgametedirectedzygoteactivationbyknoxbelltranscriptionfactorsingreenplants |