A zinc finger-dependent, PRDM13-driven mechanism regulates retinal progenitor cell fate from mouse embryonic stem cells via WNT signaling

The transcriptional regulation underlying eye field (retinal primordium) development requires precise control, yet the mechanisms guiding lineage-specific differentiation within the central nervous system (CNS) remain incompletely understood. Using neuroectoderm (NE) organoids derived from mouse embryonic stem cells, we investigate the role of PRDM13 in eye field specification. We demonstrate that Prdm13 expression inhibits RX<sup>+</sup> eye field fate but permits non-eye field NE differentiation, an effect that depends on its first and second zinc-finger domains. Prdm13 activates the WNT/β-catenin signaling pathway during differentiation, leading to downregulation of key transcription factors crucial for establishing the eye field. Pharmacological inhibition of WNT signaling abolishes PRDM13-mediated suppression, restoring RX<sup>+</sup> eye field differentiation. Our work reveals a previously undescribed PRDM13-WNT signaling axis that regulates lineage-specific neural differentiation of embryonic stem cells.

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Publication Details

Journal
Stem Cell Reports
Published
2025-05-22
DOI
https://doi.org/10.1016/j.stemcr.2025.102508
Citations
1
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.81

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article

A zinc finger-dependent, PRDM13-driven mechanism regulates retinal progenitor cell fate from mouse embryonic stem cells via WNT signaling

Jing Xu, Brian W. Basinski, Yuanhao Huang, D. Ford Hannum et al.
1 citations
Stem Cell Reports
Retinal Development and Disorders
0.81
article

A zinc finger-dependent, PRDM13-driven mechanism regulates retinal progenitor cell fate from mouse embryonic stem cells via WNT signaling

Jing Xu, Brian W. Basinski, Yuanhao Huang, D. Ford Hannum, Rajesh C. Rao, Charukesi D. Sivakumar, Qiang Li, Jie Liu, Hong Pan, Tyler J Carman
article en
1 citations

Abstract

The transcriptional regulation underlying eye field (retinal primordium) development requires precise control, yet the mechanisms guiding lineage-specific differentiation within the central nervous system (CNS) remain incompletely understood. Using neuroectoderm (NE) organoids derived from mouse embryonic stem cells, we investigate the role of PRDM13 in eye field specification. We demonstrate that Prdm13 expression inhibits RX<sup>+</sup> eye field fate but permits non-eye field NE differentiation, an effect that depends on its first and second zinc-finger domains. Prdm13 activates the WNT/β-catenin signaling pathway during differentiation, leading to downregulation of key transcription factors crucial for establishing the eye field. Pharmacological inhibition of WNT signaling abolishes PRDM13-mediated suppression, restoring RX<sup>+</sup> eye field differentiation. Our work reveals a previously undescribed PRDM13-WNT signaling axis that regulates lineage-specific neural differentiation of embryonic stem cells.

Stem Cell ReportsVol. 20(6)
University of Michigan (US), Michigan Medicine (US)
Research to Prevent Blindness, A. Alfred Taubman Medical Research Institute, E. Matilda Ziegler Foundation for the Blind, National Eye Institute
Zero hunger
Openalex Percentile: Top 28%
Retinal Development and Disorders
0.81
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A zinc finger-dependent, PRDM13-driven mechanism regulates retinal progenitor cell fate from mouse embryonic stem cells via WNT signaling — Jing Xu, Brian W. Basinski, et al. · Stem Cell Reports (2025) | TGRS Research Map | TGRS