Pathogenic variants in Crx have distinct cis-regulatory effects on enhancers and silencers in photoreceptors

• Published in: bioRxiv
• Main Authors: Shepherdson, James L, Friedman, Ryan Z, Zheng, Yiqiao, Sun, Chi, Oh, Inez Y, Granas, David M, Cohen, Barak A, Chen, Shiming, White, Michael A
• Format: Journal Article Paper
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 02.12.2023
• Subjects: Chromatin; Enhancers; Gene silencing; Phenotypes; Photoreceptors; Regulatory sequences; Reporter gene; Retinopathy
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2023.05.27.542576

Dozens of variants in the photoreceptor-specific transcription factor (TF) CRX are linked with human blinding diseases that vary in their severity and age of onset. It is unclear how different variants in this single TF alter its function in ways that lead to a range of phenotypes. We examined the effects of human disease-causing variants on CRX -regulatory function by deploying massively parallel reporter assays (MPRAs) in live mouse retinas carrying knock-ins of two variants, one in the DNA binding domain (p.R90W) and the other in the transcriptional effector domain (p.E168d2). The degree of reporter gene dysregulation caused by the variants corresponds with their phenotypic severity. The two variants affect similar sets of enhancers, while p.E168d2 has stronger effects on silencers. -regulatory elements (CREs) near cone photoreceptor genes are enriched for silencers that are de-repressed in the presence of p.E168d2. Chromatin environments of CRX-bound loci were partially predictive of episomal MPRA activity, and silencers were notably enriched among distal elements whose accessibility increases later in retinal development. We identified a set of potentially pleiotropic regulatory elements that convert from silencers to enhancers in retinas that lack a functional CRX effector domain. Our findings show that phenotypically distinct variants in different domains of CRX have partially overlapping effects on its -regulatory function, leading to misregulation of similar sets of enhancers, while having a qualitatively different impact on silencers.