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Hippo signalling regulates eye growth during embryogenesis through its effectors YAP and TAZ. Taking advantage of a  Yap  heterozygous mouse line, we here sought to examine its function in adult neural retina, where YAP expression is restricted to Müller glia. We first discovered an unexpected temporal dynamic of gene compensation. At postnatal stages,  Taz  upregulation occurs, leading to a gain of function-like phenotype characterised by EGFR signalling potentiation and delayed cell-cycle exit of retinal progenitors. In contrast,  Yap   +/−   adult retinas no longer exhibit TAZ-dependent dosage compensation. In this context,  Yap  haploinsufficiency in aged individuals results in Müller glia dysfunction, late-onset cone degeneration, and reduced cone-mediated visual response. Alteration of glial homeostasis and altered patterns of cone opsins were also observed in Müller cell-specific conditional  Yap- knockout aged mice. Together, this study highlights a novel YAP function in Müller cells for the maintenance of retinal tissue homeostasis and the preservation of cone integrity. It also suggests that YAP haploinsufficiency should be considered and explored as a cause of cone dystrophies in human.

Yap haploinsufficiency leads to Müller cell dysfunction and late-onset cone dystrophy