PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 19, 2026Horticulture Research0 citationsOpen Access

Synonymous substitutions confer the conserved WPRa4 as a novel target of miR396 in cucumber

View Full Paper
XWX WangLZLonglong ZhengZSZhihui Sun

Key Points

  • This research investigates the role of CsaWPRa4 as a target gene of miR396 and its evolutionary significance in cucumbers.
  • Predicted CsaWPRa4 as a target gene through bioinformatic analysis.
  • Confirmed negative regulation of CsaWPRa4 by miR396 using RT-qPCR and luciferase assays.
  • Utilized CRISPR/Cas9 for gene editing to create Csawpra4 mutants.
  • Assessed subcellular localization of CsaWPRa4.
  • Analyzed effects on chloroplast and flower morphogenesis-related genes.
  • CsaWPRa4 was confirmed as a target of miR396 in cucumbers through multiple experiments.
  • Synonymous substitutions were found to influence the target site within WPRa4.
  • Csawpra4 mutants displayed altered photosynthetic traits and changes in flower morphogenesis.
  • The study elucidated the role of synonymous substitutions in the evolutionary processes of miRNA-target interactions.

Abstract

Abstract As an evolutionarily conserved microRNA (miRNA), miR396 regulates plant growth by integrating developmental and environmental signals. In the present study, CsaWPRa4, a WEB1 (Weak Chloroplast Movement under Blue Light 1)/PMI2 (Plastid Movement Impaired 2)-related protein (WPR) family member, was predicted to be a novel target gene of CsamiR396 in cucumbers. WPRa4 is a highly conserved protein in plants. Interestingly, bioinformatic analysis showed that WPRa4 acts as a conserved target gene of miR396 in cucumber and its related species in cucurbits, but not in other plants. The miR396 binding site is located within the coding region of the AAK(K/R)AVE motif in WPRa4, and it evolved by synonymous substitutions in cucurbits. Negative regulation of CsaWPRa4 by CsamiR396 was confirmed by RT-qPCR, luciferase assay, gene overexpression, and TRSV-based gene silencing analysis. The subcellular localization assay showed that CsaWPRa4 was localized to both the cell periphery and nuclear periphery. Thereafter, Csawpra4 mutants were generated using CRISPR/Cas9-mediated gene editing. Chloroplast- and flower morphogenesis-related genes were altered, resulting in altered photosynthetic traits and flower morphogenesis in Csawpra4 mutants. In summary, our results showed that WPRa4 evolved as a novel target of miR396 through synonymous substitutions in cucurbits, uncovering the role of synonymous substitutions in genome evolution and providing a new perspective on miRNA-target evolutionary processes in plants.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/6996a7a5ecb39a600b3ed81dhttps://doi.org/10.1093/hr/uhag036
Ask AI
Helpful
Bookmark
Share
View Full Paper