Eight hydroxyproline-O-galactosyltransferases play essential roles in female reproductive development.

Arabinogalactan-Proteins Female gametophyte development Hyp-Galactosyltransferases Plant reproduction Pollen-pistil interactions

Journal

Plant science : an international journal of experimental plant biology
ISSN: 1873-2259
Titre abrégé: Plant Sci
Pays: Ireland
ID NLM: 9882015

Informations de publication

Date de publication:
16 Aug 2024
Historique:
received: 14 06 2024
revised: 13 08 2024
accepted: 14 08 2024
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 18 8 2024
Statut: aheadofprint

Résumé

In angiosperms, ovules give rise to seeds upon fertilization. Thus, seed formation is dependent on both successful ovule development and tightly controlled communication between female and male gametophytes. During establishment of these interactions, cell walls play a pivotal role, especially arabinogalactan-proteins (AGPs). AGPs are highly glycosylated proteins decorated by arabinogalactan side chains, representing 90% of the AGP molecule. AGP glycosylation is initiated by a reaction catalysed by hydroxyproline-O-galactosyltransferases (Hyp-GALTs), specifically eight of them (GALT2-9), which add the first galactose to Hyp residues. Five Hyp-GALTs (GALT2, 5, 7, 8 and 9) were previously described as essential for AGP functions in pollen and ovule development, pollen-pistil interactions, and seed morphology. In the present work, a higher order Hyp-GALT mutant (23456789) was studied, with a high degree of under-glycosylated AGPs, to gain deeper insight into the crucial roles of these eight enzymes in female reproductive tissues. Notably, the 23456789 mutant demonstrated a high quantity of unfertilized ovules, displaying abnormal callose accumulation both at the micropylar region and, sometimes, throughout the entire embryo sac. Additionally, this mutant displayed ovules with abnormal embryo sacs, had a disrupted spatiotemporal distribution of AGPs in female reproductive tissues, and showed abnormal seed and embryo development, concomitant with a reduction in AGP-GlcA levels. This study revealed that at least three more enzymes exhibit Hyp-O-GALT activity in Arabidopsis (GALT3, 4 and 6), and reinforces the crucial importance of AGP carbohydrates in carrying out the biological functions of AGPs during plant reproduction.

Identifiants

pubmed: 39154893
pii: S0168-9452(24)00258-9
doi: 10.1016/j.plantsci.2024.112231
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112231

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Conflict of Interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Diana Moreira (D)

LAQV Requimte, Sustainable Chemistry, Departamento de Biologia, Faculdade de Ciências da Universidade do Porto, 4169-007 Porto, Portugal.

Dasmeet Kaur (D)

Department of Environmental & Plant Biology, Ohio University, Athens, OH 45701-2979, USA; Molecular and Cellular Biology Program, Ohio University, Athens, OH 45701-2979, USA.

Sara Fourbert-Mendes (S)

LAQV Requimte, Sustainable Chemistry, Departamento de Biologia, Faculdade de Ciências da Universidade do Porto, 4169-007 Porto, Portugal.

Allan M Showalter (AM)

Department of Environmental & Plant Biology, Ohio University, Athens, OH 45701-2979, USA; Molecular and Cellular Biology Program, Ohio University, Athens, OH 45701-2979, USA.

Sílvia Coimbra (S)

LAQV Requimte, Sustainable Chemistry, Departamento de Biologia, Faculdade de Ciências da Universidade do Porto, 4169-007 Porto, Portugal.

Ana Marta Pereira (AM)

LAQV Requimte, Sustainable Chemistry, Departamento de Biologia, Faculdade de Ciências da Universidade do Porto, 4169-007 Porto, Portugal. Electronic address: ambacpereira@fc.up.pt.

Classifications MeSH