Cargando…

Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces

Although the main players of the strigolactone (SL) signaling pathway have been characterized genetically, how they regulate plant development is still poorly understood. Of central importance are the SUPPRESSOR OF MAX2 1-LIKE (SMXL) proteins that belong to a family of eight members in Arabidopsis t...

Descripción completa

Detalles Bibliográficos
Autores principales: Temmerman, Arne, Guillory, Ambre, Bonhomme, Sandrine, Goormachtig, Sofie, Struk, Sylwia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133912/
https://www.ncbi.nlm.nih.gov/pubmed/35645992
http://dx.doi.org/10.3389/fpls.2022.887232
_version_ 1784713679086813184
author Temmerman, Arne
Guillory, Ambre
Bonhomme, Sandrine
Goormachtig, Sofie
Struk, Sylwia
author_facet Temmerman, Arne
Guillory, Ambre
Bonhomme, Sandrine
Goormachtig, Sofie
Struk, Sylwia
author_sort Temmerman, Arne
collection PubMed
description Although the main players of the strigolactone (SL) signaling pathway have been characterized genetically, how they regulate plant development is still poorly understood. Of central importance are the SUPPRESSOR OF MAX2 1-LIKE (SMXL) proteins that belong to a family of eight members in Arabidopsis thaliana, of which one subclade is involved in SL signaling and another one in the pathway of the chemically related karrikins. Through proteasomal degradation of these SMXLs, triggered by either DWARF14 (D14) or KARRIKIN INSENSITIVE2 (KAI2), several physiological processes are controlled, such as, among others, shoot and root architecture, seed germination, and seedling photomorphogenesis. Yet another clade has been shown to be involved in vascular development, independently of the D14 and KAI2 actions and not relying on proteasomal degradation. Despite their role in several aspects of plant development, the exact molecular mechanisms by which SMXLs regulate them are not completely unraveled. To fill the major knowledge gap in understanding D14 and KAI2 signaling, SMXLs are intensively studied, making it challenging to combine all the insights into a coherent characterization of these important proteins. To this end, this review provides an in-depth exploration of the recent data regarding their physiological function, evolution, structure, and molecular mechanism. In addition, we propose a selection of future perspectives, focusing on the apparent localization of SMXLs in subnuclear speckles, as observed in transient expression assays, which we couple to recent advances in the field of biomolecular condensates and liquid–liquid phase separation.
format Online
Article
Text
id pubmed-9133912
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-91339122022-05-27 Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces Temmerman, Arne Guillory, Ambre Bonhomme, Sandrine Goormachtig, Sofie Struk, Sylwia Front Plant Sci Plant Science Although the main players of the strigolactone (SL) signaling pathway have been characterized genetically, how they regulate plant development is still poorly understood. Of central importance are the SUPPRESSOR OF MAX2 1-LIKE (SMXL) proteins that belong to a family of eight members in Arabidopsis thaliana, of which one subclade is involved in SL signaling and another one in the pathway of the chemically related karrikins. Through proteasomal degradation of these SMXLs, triggered by either DWARF14 (D14) or KARRIKIN INSENSITIVE2 (KAI2), several physiological processes are controlled, such as, among others, shoot and root architecture, seed germination, and seedling photomorphogenesis. Yet another clade has been shown to be involved in vascular development, independently of the D14 and KAI2 actions and not relying on proteasomal degradation. Despite their role in several aspects of plant development, the exact molecular mechanisms by which SMXLs regulate them are not completely unraveled. To fill the major knowledge gap in understanding D14 and KAI2 signaling, SMXLs are intensively studied, making it challenging to combine all the insights into a coherent characterization of these important proteins. To this end, this review provides an in-depth exploration of the recent data regarding their physiological function, evolution, structure, and molecular mechanism. In addition, we propose a selection of future perspectives, focusing on the apparent localization of SMXLs in subnuclear speckles, as observed in transient expression assays, which we couple to recent advances in the field of biomolecular condensates and liquid–liquid phase separation. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9133912/ /pubmed/35645992 http://dx.doi.org/10.3389/fpls.2022.887232 Text en Copyright © 2022 Temmerman, Guillory, Bonhomme, Goormachtig and Struk. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Temmerman, Arne
Guillory, Ambre
Bonhomme, Sandrine
Goormachtig, Sofie
Struk, Sylwia
Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title_full Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title_fullStr Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title_full_unstemmed Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title_short Masks Start to Drop: Suppressor of MAX2 1-Like Proteins Reveal Their Many Faces
title_sort masks start to drop: suppressor of max2 1-like proteins reveal their many faces
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133912/
https://www.ncbi.nlm.nih.gov/pubmed/35645992
http://dx.doi.org/10.3389/fpls.2022.887232
work_keys_str_mv AT temmermanarne masksstarttodropsuppressorofmax21likeproteinsrevealtheirmanyfaces
AT guilloryambre masksstarttodropsuppressorofmax21likeproteinsrevealtheirmanyfaces
AT bonhommesandrine masksstarttodropsuppressorofmax21likeproteinsrevealtheirmanyfaces
AT goormachtigsofie masksstarttodropsuppressorofmax21likeproteinsrevealtheirmanyfaces
AT struksylwia masksstarttodropsuppressorofmax21likeproteinsrevealtheirmanyfaces