Cited by 2Photosynthetic Processes and MechanismsLight effects on plantsPlant biochemistry and biosynthesis

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The variegated canalized-1 tomato mutant is linked to photosystem assembly

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Wijesingha Ahchige, Micha, Fisher, Josef, Sokolowska, Ewelina, Lyall, Rafe, Illing, Nicola, Skirycz, Aleksandra, Zamir, Dani, Alseekh, Saleh, Fernie, Alisdair R.·2024·Computational and Structural Biotechnology Journal

Published version of a preprint

Abstract

The recently described canal-1 tomato mutant, which has a variegated leaf phenotype, has been shown to affect canalization of yield. The corresponding protein is orthologous to AtSCO2 -SNOWY COTYLEDON 2, which has suggested roles in thylakoid biogenesis. Here we characterize the canal-1 mutant through a multi-omics approach, by comparing mutant to wild-type tissues. While white canal-1 leaves are devoid of chlorophyll, green leaves of the mutant appear wild-type-like, despite an impaired protein function. Transcriptomic data suggest that green mutant leaves compensate for this impaired protein function by upregulation of transcription of photosystem assembly and photosystem component genes, thereby allowing adequate photosystem establishment, which is reflected in their wild-type-like proteome. White canal-1 leaves, however, likely fail to reach a certain threshold enabling this overcompensation, and plastids get trapped in an undeveloped state, while additionally suffering from high light stress, indicated by the overexpression of ELIP homolog genes. The metabolic profile of white and to a lesser degree also green tissues revealed upregulation of amino acid levels, that was at least partially mediated by transcriptional and proteomic upregulation. These combined changes are indicative of a stress response and suggest that white tissues behave as carbon sinks. In summary, our work demonstrates the relevance of the SCO2 protein in both photosystem assembly and as a consequence in the canalization of yield.

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Metadata

Authors
Wijesingha Ahchige, M., Fisher, J., Sokolowska, E., Lyall, R., Illing, N., Skirycz, A., Zamir, D., Alseekh, S., & Fernie, A. R.
Affiliations
  • Root Biology and Symbiosis, Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476 Potsdam-Golm, Germany
  • Hebrew University of Jerusalem (IL)
  • University of Cape Town (ZA)
  • Max Planck Institute of Molecular Plant Physiology (DE)
  • Center of Plant Systems Biology and Biotechnology (BG)
Corresponding author
  • Alseekh, Saleh
  • Fernie, Alisdair R.
Venue
Computational and Structural Biotechnology Journal
Published
2024-10-24
Volume
23
Pages
3967-3988
ISSN
2001-0370 (ISSN-L)
OpenAlex
W4403711916
Cited by
2
References
1
Citations by year
2025: 2
FWCI
0.27
Type
journal article
Language
en
Open access
Locations
  • Computational and Structural Biotechnology Journal (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Funders
  • Horizon 2020 Framework Programme
  • European Regional Development Fund
  • HORIZON EUROPE Widening Participation and Strengthening the European Research Area
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Keywords
photosystem assembly, thylakoid biogenesis, SCO2, chlorophyll deficiency, variegated leaves, plastid development, high light stress, amino acid metabolism, carbon sink, transcriptomics, proteomics, metabolomics

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