Temporal Transcriptomic Profiling of the Developing Xenopus laevis Eye

Retinal progenitor cells (RPCs) are a multipotent and highly proliferative population that give rise to all retinal cell types during organogenesis. Defining their molecular signature is a key step towards identifying suitable approaches to treat visual impairments. Here, we performed RNA sequencing of whole eyes from <i>Xenopus</i> at three embryonic stages and used differential expression analysis to define the transcriptomic profiles of optic tissues containing proliferating and differentiating RPCs during retinogenesis. Gene Ontology and KEGG pathway analyses showed that genes associated with developmental pathways (including Wnt and Hedgehog signaling) were upregulated during the period of active RPC proliferation in early retinal development (Nieuwkoop Faber st. 24 and 27). Developing eyes had dynamic expression profiles and shifted to enrichment for metabolic processes and phototransduction during RPC progeny specification and differentiation (st. 35). Furthermore, conserved adult eye regeneration genes were also expressed during early retinal development, including <i>sox2</i>, <i>pax6</i>, <i>nrl</i>, and Notch signaling components. The eye transcriptomic profiles presented here span RPC proliferation to retinogenesis and include regrowth-competent stages. Thus, our dataset provides a rich resource to uncover molecular regulators of RPC activity and will allow future studies to address regulators of RPC proliferation during eye repair and regrowth.

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Publication Details

Journal
Cells
Published
2024-08-21
DOI
https://doi.org/10.3390/cells13161390
Citations
2
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.47

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article

Temporal Transcriptomic Profiling of the Developing Xenopus laevis Eye

Samantha J. Hack, Kelly Ai-Sun Tseng, Juli Petereit
2 citations
Cells
Retinal Development and Disorders
0.47
article

Temporal Transcriptomic Profiling of the Developing Xenopus laevis Eye

Samantha J. Hack, Kelly Ai-Sun Tseng, Juli Petereit
article en
2 citations

Abstract

Retinal progenitor cells (RPCs) are a multipotent and highly proliferative population that give rise to all retinal cell types during organogenesis. Defining their molecular signature is a key step towards identifying suitable approaches to treat visual impairments. Here, we performed RNA sequencing of whole eyes from <i>Xenopus</i> at three embryonic stages and used differential expression analysis to define the transcriptomic profiles of optic tissues containing proliferating and differentiating RPCs during retinogenesis. Gene Ontology and KEGG pathway analyses showed that genes associated with developmental pathways (including Wnt and Hedgehog signaling) were upregulated during the period of active RPC proliferation in early retinal development (Nieuwkoop Faber st. 24 and 27). Developing eyes had dynamic expression profiles and shifted to enrichment for metabolic processes and phototransduction during RPC progeny specification and differentiation (st. 35). Furthermore, conserved adult eye regeneration genes were also expressed during early retinal development, including <i>sox2</i>, <i>pax6</i>, <i>nrl</i>, and Notch signaling components. The eye transcriptomic profiles presented here span RPC proliferation to retinogenesis and include regrowth-competent stages. Thus, our dataset provides a rich resource to uncover molecular regulators of RPC activity and will allow future studies to address regulators of RPC proliferation during eye repair and regrowth.

CellsVol. 13(16)
University of Nevada, Las Vegas (US), University of Nevada, Reno (US), Western Michigan University (US)
Western Michigan University, National Institutes of Health
Openalex Percentile: Top 36%
Retinal Development and Disorders
0.47
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Temporal Transcriptomic Profiling of the Developing Xenopus laevis Eye — Samantha J. Hack, Kelly Ai-Sun Tseng, et al. · Cells (2024) | TGRS Research Map | TGRS