Study of the molecular basis of inherited eye disorders with a focus on the role of microRNAs

Inherited eye diseases are a common cause of visual impairment in children and young adults. They include both neurodegenerative forms, including, among others, retinitis pigmentosa (RP), Stargardt Disease and Leber Congenital Amaurosis (LCA), and developmental defects, such as microphthalmia, anophthalmia and coloboma. All these diseases are characterized by extensive genetic heterogeneity, which constitutes an obstacle both for accurate diagnosis and when devising effective gene-based treatments.
In the past 15 years, we have focused our efforts on the elucidation of the role of microRNAs in eye development and function, in both physiological and pathological conditions. In particular, we have generated the most comprehensive atlas of microRNA expression data (miRNome) in the eye available to date, first based on RNA in situ hybridization and subsequently on next generation sequencing (NGS) approaches. We have identified the first microRNA responsible for a monogenic form of ocular disease, namely miR-204, which is mutated in an autosomal dominant RP. We also demonstrated that the Adeno-Associated Viral (AAV) administration of miR-204 exerts a protective effect on photoreceptors in different models of inherited degenerations in a mutation/gene-independent manner. We are now extending this analysis to additional microRNAs that represent potential mutation-independent therapeutic tools for inherited eye diseases. We believe that this strategy may represent a valid alternative/complementary approach to gene-based therapy and could be extended to a larger portion of patients in the near future. Finally, we also aim to shed light on the “missing heritability” of a significant fraction of patients with Inherited eye diseases who remain undiagnosed even after extensive NGS-based genomic approaches, such as targeted or whole exome sequencing using an integrated strategy aimed at the search for structural variants and single nucleotide variants with an impact on transcript integrity.

The "Total Award" amount indicated for this project represents the share of the funding of the Telethon Foundation for research by the Tigem institute from January 2022 until last budget year, calculated based on the size of the research group.