Cargando…
FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum
The identification downstream genes of floral organ identity regulators are critical to revealing the molecular mechanisms underlying floral morphogenesis. However, a general regulatory pathway between floral organ identity genes and their downstream targets is still unclear because of the lack of s...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694435/ https://www.ncbi.nlm.nih.gov/pubmed/36430880 http://dx.doi.org/10.3390/ijms232214403 |
_version_ | 1784837798685048832 |
---|---|
author | Ma, Zhiyuan Yang, Qingyu Zeng, Lingtian Li, Jiayi Jiao, Xinyu Liu, Zhixiong |
author_facet | Ma, Zhiyuan Yang, Qingyu Zeng, Lingtian Li, Jiayi Jiao, Xinyu Liu, Zhixiong |
author_sort | Ma, Zhiyuan |
collection | PubMed |
description | The identification downstream genes of floral organ identity regulators are critical to revealing the molecular mechanisms underlying floral morphogenesis. However, a general regulatory pathway between floral organ identity genes and their downstream targets is still unclear because of the lack of studies in nonmodel species. Here, we screened a direct downstream target gene, FaesELF3, of a stamen identity transcription factor, FaesAP3_1, in long-homostyle (LH) Fagopyrum esculentum moench by using yeast one-hybrid (Y1H) and dual-luciferase reporter (DR) assays. Furthermore, FaesAP3_1-silenced LH plants that produced flowers with part stamens or anthers homeotically converted into a tepaloid structure, and FaesELF3-silenced plants that had flowers with part stamens consisting of a short filament and empty anther (male sterile anther). All these suggested that transcription factor (TF) FaesAP3_1 directly activates FaesELF3 in order to regulate filament elongation and pollen grain development in LH buckwheat. Our data also suggested that other stamen development pathways independent of FaesAP3_1 remain in F. esculentum. |
format | Online Article Text |
id | pubmed-9694435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96944352022-11-26 FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum Ma, Zhiyuan Yang, Qingyu Zeng, Lingtian Li, Jiayi Jiao, Xinyu Liu, Zhixiong Int J Mol Sci Article The identification downstream genes of floral organ identity regulators are critical to revealing the molecular mechanisms underlying floral morphogenesis. However, a general regulatory pathway between floral organ identity genes and their downstream targets is still unclear because of the lack of studies in nonmodel species. Here, we screened a direct downstream target gene, FaesELF3, of a stamen identity transcription factor, FaesAP3_1, in long-homostyle (LH) Fagopyrum esculentum moench by using yeast one-hybrid (Y1H) and dual-luciferase reporter (DR) assays. Furthermore, FaesAP3_1-silenced LH plants that produced flowers with part stamens or anthers homeotically converted into a tepaloid structure, and FaesELF3-silenced plants that had flowers with part stamens consisting of a short filament and empty anther (male sterile anther). All these suggested that transcription factor (TF) FaesAP3_1 directly activates FaesELF3 in order to regulate filament elongation and pollen grain development in LH buckwheat. Our data also suggested that other stamen development pathways independent of FaesAP3_1 remain in F. esculentum. MDPI 2022-11-19 /pmc/articles/PMC9694435/ /pubmed/36430880 http://dx.doi.org/10.3390/ijms232214403 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ma, Zhiyuan Yang, Qingyu Zeng, Lingtian Li, Jiayi Jiao, Xinyu Liu, Zhixiong FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title | FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title_full | FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title_fullStr | FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title_full_unstemmed | FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title_short | FaesAP3_1 Regulates the FaesELF3 Gene Involved in Filament-Length Determination of Long-Homostyle Fagopyrum esculentum |
title_sort | faesap3_1 regulates the faeself3 gene involved in filament-length determination of long-homostyle fagopyrum esculentum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694435/ https://www.ncbi.nlm.nih.gov/pubmed/36430880 http://dx.doi.org/10.3390/ijms232214403 |
work_keys_str_mv | AT mazhiyuan faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum AT yangqingyu faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum AT zenglingtian faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum AT lijiayi faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum AT jiaoxinyu faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum AT liuzhixiong faesap31regulatesthefaeself3geneinvolvedinfilamentlengthdeterminationoflonghomostylefagopyrumesculentum |