Evidence map›Paper›PMID 40926682›Full record

ArticleAnnals of botany2026

Exploring the role of β-1,3-glucanase in aerenchyma development in sugarcane roots.

Grayce Hellen Romim, Eveline Q P Tavares, Adriana Grandis, Lauana P de Oliveira, Diego Demarco, Giovanna Gramegna, William V M Mira, Bruno V Navarro, Marcos S Buckeridge

Abstract read
In one paragraph

Article in Annals of botany, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Grayce Hellen RomimLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0002-1728-0876
Eveline Q P TavaresLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0002-9340-7955
Adriana GrandisLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0002-8416-3733
Lauana P de OliveiraLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0001-9622-7020
Diego DemarcoLaboratório de Anatomia Vegetal, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0002-8244-2608
Giovanna GramegnaLaboratório de Genética Molecular de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0001-8585-7801
William V M MiraLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0001-8592-9000
Bruno V NavarroLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0001-9289-4328
Marcos S BuckeridgeLaboratório de Fisiologia Ecológica de Plantas, Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, São Paulo 05508090, Brazil.ORCID 0000-0002-5455-8136

Funding

National Institute of Bioethanol Science and Technology 2014/50884-5National Institute of Bioethanol Science and Technology 465319/2014-9Research Center of Greenhouse Gas Innovation (RCGI) 142090/2018-2Research Center of Greenhouse Gas Innovation (RCGI) 2011/07586-5Research Center of Greenhouse Gas Innovation (RCGI) 2014/50279-4Research Center of Greenhouse Gas Innovation (RCGI) 2015/01260-1Research Center of Greenhouse Gas Innovation (RCGI) 2019/13936Research Center of Greenhouse Gas Innovation (RCGI) 2020/15230-5Research Center of Greenhouse Gas Innovation (RCGI) 2022/00441-6Research Center of Greenhouse Gas Innovation (RCGI) 371055
6 · The paper itself

Abstract

BACKGROUND AND

aimsAerenchyma formation has emerged as a promising model for understanding cell wall modifications. Certain cells undergo programmed cell death, whereas others do not, suggesting the existence of a tightly regulated signalling dispersion mechanism. Cell-to-cell communication occurs via plasmodesmata, whose permeability is regulated by the deposition of callose (β-1,3-glucan) and its degradation by β-1,3-glucanase. These processes might be key to understanding the selection of specific cells, which modify their cell walls for aerenchyma formation. Therefore, the aim of this study was to characterize the role of callose and β-1,3-glucanase during aerenchyma formation.

methodsSugarcane roots were segmented into five sections, each 1 cm in length, and embedded in LR White resin. Semi-thin sections were obtained, and immunolocalization was performed using monoclonal antibodies for the polysaccharides callose (β-1,3-glucan) and mixed-linkage β-1,3-1,4-glucan. The protein for in situ localization was chosen based on its ontology and protein domain structure. A super-resolution microscope was used to identify the antibody signal deposition pattern. KEY

resultsThe antibody signal against mixed-linkage β-1,3-1,4-glucan was detected continuously along the cell wall in the early root segments. Its removal and degradation became evident from the third segment onwards, coinciding with aerenchyma formation. In contrast, callose exhibited a punctate signal, possibly marking regions of plasmodesmata. Callose degradation followed a similar pattern to that of mixed-linkage β-1,3-1,4-glucan (segment 3-segment 5), although its signal was less abundant. The β-1,3-glucanase showed peak signal from segment 3 to segment 4, accompanied by a punctate signal, suggesting its action at regions of plasmodesmata and callose degradation sites.

conclusionThe presence of callose raises critical questions about how cells transmit signals and why only certain cells undergo programmed cell death. Managing the permeability and selectivity of intercellular communication might be a key factor in various biological processes. Gaining insight into these mechanisms and identifying potential enzymes and polysaccharides could provide new perspectives for future research.

Indexed as

Glucan 1,3-beta-GlucosidasePlant ProteinsPlant RootsSaccharumCell WallGlucansPlasmodesmatacalloseGlucan 1,3-beta-GlucosidaseGlucansPlant ProteinsAerenchymacallosecell communicationcell wallglycosyl hydrolase family 17plasmodesmata

Identifiers

PMID40926682
PMCPMC12784069

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.