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January 18, 2026Plant and Cell Physiology0 citationsOpen Access

Elongator Complex Differentially Regulates Transcription and Translation In Hypocotyl and Cotyledons During Early Light-Dependent Arabidopsis Development

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MJMagdalena Jarosz-OstrówkaMKMałgorzata Kwaśniak-OwczarekNMNatalia Małecka

Key Points

  • This research aims to explore how the Elongator complex influences transcription and translation during the early light-dependent development of Arabidopsis.
  • Analyzed photomorphogenic responses in Arabidopsis thaliana
  • Used RNA-Seq and miRNA-Seq to assess gene expression profiles
  • Compared the developmental effects of elo3–6 mutant with urm11 urm12 mutant and their triple mutant
  • elo3–6 mutant showed elongated hypocotyl and abnormal cotyledon development
  • Distinct dysregulated gene sets identified in hypo and cotyledon tissues
  • Defects in chloroplast physiology and auxin responses linked to hypocotyl elongation
  • Increased tolerance to translation inhibitors was observed in the mutants
  • Feedback mechanism indicates inefficient translation impacts mRNA abundance

Abstract

Abstract During Arabidopsis thaliana photomorphogenesis, light promotes cotyledon expansion and inhibits hypocotyl elongation. This process involves transcriptional reprogramming controlled by various factors, including the Elongator complex which regulates gene expression at the level of transcription and translation via epigenetic and tRNA modifications, respectively. The elo3–6 mutant, lacking Elongator activity, exhibited photomorphogenic defects: less open, hyponastic cotyledons and an elongated hypocotyl. RNA-Seq and miRNA-Seq revealed distinct dysregulated gene sets in elo3–6 hypocotyl and cotyledons. In hypocotyl, the elo3–6 defect affected expression of genes involved in chloroplast physiology, circadian regulation, and auxin responses. Impaired chloroplast biogenesis apparently triggered retrograde signaling and a hypoxia-like state, preventing full inhibition of hypocotyl elongation. The defective elo3–6 cotyledon development is likely due to compromised translation. This was supported by the presence of similar morphological defects in urm11 urm12, defective in the same type of tRNA modification as in elo3–6, and the synergism observed in the elo3–6 urm11 urm12 (euu) triple mutant showing seedling lethality. Moreover, elo3–6 and urm11 urm12 showed increased tolerance to translation inhibitors, including hygromycin B which prevented the narrower cotyledon opening in elo3–6, suggesting that strong Elongator-dependent codon-anticodon interactions are required for proper cotyledon development. Interestingly, the genes enriched in codons recognized by tRNA anticodons modified by Elongator showed decreased mRNA abundance in elo3–6, suggesting a feedback mechanism downregulating the abundance of inefficiently translated mRNAs. Our results suggest that Elongator’s transcriptional role is more important in hypocotyl growth, while its translational role is more prominent in cotyledon development.

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Cite This Study

Jarosz-Ostrówka et al. (2026) studied this question.

synapsesocial.com/papers/696c7835eb60fb80d1396783https://doi.org/10.1093/pcp/pcag005
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