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髓磷脂调节因子(MYRF)是视网膜色素上皮发育的关键早期调节因子。

Myelin regulatory factor (MYRF) is a critical early regulator of retinal pigment epithelial development.

作者信息

Brinkmeier Michelle L, Wang Su Qing, Pittman Hannah A, Cheung Leonard Y, Prasov Lev

机构信息

Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan, United States of America.

Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.

出版信息

PLoS Genet. 2025 Apr 15;21(4):e1011670. doi: 10.1371/journal.pgen.1011670. eCollection 2025 Apr.

Abstract

Myelin regulatory factor (Myrf) is a critical transcription factor in early retinal and retinal pigment epithelial development, and human variants in MYRF are a cause for nanophthalmos. Single cell RNA sequencing (scRNAseq) was performed on Myrf conditional knockout mice (Rx > Cre Myrffl/fl) at 3 developmental timepoints. Myrf was expressed specifically in the RPE, and expression was abrogated in Rx > Cre Myrffl/fl eyes. scRNAseq analysis revealed a loss of RPE cells at all timepoints resulting from cell death. GO-term analysis in the RPE revealed downregulation of melanogenesis and anatomic structure morphogenesis pathways, which were supported by electron microscopy and histologic analysis. Novel structural target genes including Ermn and Upk3b, along with macular degeneration and inherited retinal disease genes were identified as downregulated, and a strong upregulation of TGFß/BMP signaling and effectors was observed. Regulon analysis placed Myrf downstream or parallel to Pax6 and Mitf and upstream of Sox10 in RPE differentiation. Together, these results suggest a strong role for MYRF in the RPE maturation by regulating melanogenesis, cell survival, and cell structure, in part acting through suppression of TGFß signaling and activation of Sox10.

摘要

髓磷脂调节因子(Myrf)是视网膜和视网膜色素上皮早期发育中的关键转录因子,MYRF基因的人类变异是小眼球症的病因。在3个发育时间点对Myrf条件性敲除小鼠(Rx > Cre Myrffl/fl)进行了单细胞RNA测序(scRNAseq)。Myrf在视网膜色素上皮(RPE)中特异性表达,在Rx > Cre Myrffl/fl小鼠眼中其表达被消除。scRNAseq分析显示,在所有时间点RPE细胞均因细胞死亡而减少。对RPE的基因本体(GO)术语分析显示,黑色素生成和解剖结构形态发生途径下调,这得到了电子显微镜和组织学分析的支持。包括Ermn和Upk3b在内的新结构靶基因以及黄斑变性和遗传性视网膜疾病相关基因被确定为下调,同时观察到转化生长因子β(TGFß)/骨形态发生蛋白(BMP)信号传导及其效应分子的强烈上调。调控子分析表明,在RPE分化过程中,Myrf位于Pax6和小眼畸形相关转录因子(Mitf)的下游或与之平行,位于Sox10的上游。这些结果共同表明,MYRF在RPE成熟过程中通过调节黑色素生成、细胞存活和细胞结构发挥重要作用,部分是通过抑制TGFß信号传导和激活Sox10来实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6070/12052213/dc00d43966b8/pgen.1011670.g001.jpg

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