Evidence map›Paper›PMID 42372108›Full record

ArticlePlant physiology2026

CYSTEINE-RICH RLK2 regulates development via callose synthase-dependent symplastic transport in Arabidopsis.

Adam Zeiner, Julia Krasensky-Wrzaczek, Sunita Jindal, Yanbiao Sun, David Ušák, Jakub Hajný, Mansi Sharma, Filis Morina, Elisa Andresen, Mirva Pääkkönen and 5 more

Abstract read
In one paragraph

Article in Plant physiology, 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

15 authors.

Adam ZeinerInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0001-6366-5075
Julia Krasensky-WrzaczekInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0002-5989-9984
Sunita JindalInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0002-0318-2204
Yanbiao SunDepartment of Plant Biology, Linnean Center for Plant Biology, Swedish University of Agricultural Sciences, Almas allé 5, Uppsala 756 51, Sweden.ORCID 0000-0001-5456-845X
David UšákInstitute of Experimental Botany, Czech Academy of Sciences, Rozvojová 263, Prague 165 02, Czech Republic.ORCID 0009-0000-8432-5694
Jakub HajnýLaboratory of Growth Regulators, Faculty of Science, Palacký University & Institute of Experimental Botany of the Czech Academy of Sciences, Šlechtitelů 27, Olomouc 77900, Czech Republic.ORCID 0000-0003-2140-7195
Mansi SharmaInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0009-0008-5699-4637
Filis MorinaInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0003-1521-125X
Elisa AndresenInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0002-7201-2508
Mirva PääkkönenTurku Bioscience Centre, University of Turku and Åbo Akademi University, Tykistökatu 6, Turku 20520, Finland.ORCID 0000-0002-3184-3938
Hendrik KüpperInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0003-0712-7023
Johannes MerilahtiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Tykistökatu 6, Turku 20520, Finland.ORCID 0000-0002-9113-5175
Roman PleskotInstitute of Experimental Botany, Czech Academy of Sciences, Rozvojová 263, Prague 165 02, Czech Republic.ORCID 0000-0003-0436-9748
Charles W MelnykDepartment of Plant Biology, Linnean Center for Plant Biology, Swedish University of Agricultural Sciences, Almas allé 5, Uppsala 756 51, Sweden.ORCID 0000-0003-3251-800X
Michael WrzaczekInstitute of Plant Molecular Biology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice 370 05, Czech Republic.ORCID 0000-0002-5946-9060

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CYSTEINE-RICH RECEPTOR-LIKE PROTEIN KINASEs (CRKs) play an important role in plant development and stress responses. One of the best described members of the Arabidopsis CRK family is CRK2, which was proposed as a crucial regulator of intercellular transport facilitated by plasmodesmata (PD). As intercellular channels allowing symplastic communication, PD-mediated transport is predominantly regulated by callose synthase (CALS)-mediated callose deposition. This process can impact not just the distribution of molecules between adjacent cells, but also the symplastic loading of vascular tissue, thereby influencing plant stress responses and developmental processes. Here we described the overlapping expression pattern of genes encoding phylogenetically closely related CALS1 and CALS3. Both CALSs were phosphorylated in vitro by CRK2, and the genetic interaction between genes encoding CRK2 and CALS1 or CALS3 revealed their impact on callose deposition, rosette growth, primary root length, and development, represented as a decreased number of true leaves. Importantly, we observed significant accumulation of starch in crk2 mutant plants, especially in developmentally older leaves, which was reverted by the independent introduction of cals1.5 and cals3.1 into the crk2 mutant background. The observed starch accumulation was accompanied by photosynthesis inhibition. We propose that the growth and developmental alterations of crk2 are caused by decreased phloem loading, which resulted in starch accumulation in source organs, and subsequent sink tissue starvation. Our results propose CRK2 as negative regulator of CALS1 and CALS3 regulating source to sink transport, which impacts plant growth and development.

Indexed as

ArabidopsisArabidopsis ProteinsGlucosyltransferasesProtein Serine-Threonine KinasesBiological TransportGene Expression Regulation, PlantGlucansMutationPhosphorylationPhylogenyPlant LeavesPlant RootsPlasmodesmataProtein Kinases1,3-beta-glucan synthaseArabidopsis ProteinsAt4g18710 protein, ArabidopsiscalloseGlucansGlucosyltransferasesProtein KinasesProtein Serine-Threonine Kinases

Identifiers

PMID42372108
PMCPMC13591406

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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.