# Spatial regulation of ribosomal protein gene expression revealed by spatial transcriptomic analysis in the water fern Ceratopteris richardii

**Authors:** Jin Han, Gui-Sheng Li

PMC · DOI: 10.3389/fpls.2025.1728120 · Frontiers in Plant Science · 2026-01-19

## TL;DR

This study uses spatial transcriptomics to explore gene expression patterns in the water fern Ceratopteris richardii, revealing spatial regulation of ribosomal protein genes.

## Contribution

The study identifies spatially regulated ribosomal protein gene expression in plant tissues using spatial transcriptomics in Ceratopteris richardii.

## Key findings

- Eleven distinct tissue clusters were identified, including leaves, SAM, stem, vasculature, and scales/trichomes.
- Ribosomal protein genes showed differential expression across tissues, with some paralogs showing distinct patterns.
- In situ hybridization confirmed RP gene expression in SAM, leaf primordia, and vasculature.

## Abstract

Spatial transcriptomics is proving to be a powerful tool in elucidating plant development complexities. A study on the water fern Ceratopteris richardii applied this technology to sporophyte development, identifying 11 distinct spot clusters that mapped to leaves at various stages and probably leaf primordia and the shoot apical meristem (SAM), the stem, the vasculature, and scales/trichomes. Several transcription factors were identified—from the ARF, GRF, AP2, and bZIP families—as marker genes for these clusters. Functional enrichment analysis of marker genes identified biologically important processes, such as chloroplast-related functions in advanced leaves and DNA helicase activity in mitotic tissues. The pervasive enrichment of ribosome-related functions in nearly all tissue domains was unexpected. Furthermore, ribosomal protein (RP) genes were differentially expressed between tissues, marking single or multiple tissues. Paralogs encoding the same type of RP also differed in expression patterns from one another, with certain members not expressed or uniformly expressed. in situ hybridization showed that RP genes were generally expressed in the SAM, leaf primordia, and the vasculature.

## Linked entities

- **Genes:** CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029], GHRH (growth hormone releasing hormone) [NCBI Gene 2691], FABP4 (fatty acid binding protein 4) [NCBI Gene 2167], bZIP (basic leucine-zipper 8) [NCBI Gene 843221]
- **Species:** Ceratopteris richardii (taxon 49495)

## Full-text entities

- **Genes:** GHRH (growth hormone releasing hormone) [NCBI Gene 2691] {aka GHRF, GRF, INN}, TFAP2A (transcription factor AP-2 alpha) [NCBI Gene 7020] {aka AP-2, AP-2alpha, AP2TF, BOFS, TFAP2}
- **Species:** Ceratopteris richardii (species) [taxon 49495]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12862073/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862073/full.md

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Source: https://tomesphere.com/paper/PMC12862073