Find in Library

Establishing apicobasal polarity, involving intricate interactions among polarity regulators, is key for epithelial cell function. Though phosphatase of regenerating liver (PRL) proteins are implicated in diverse biological processes, including cancer, their developmental role remains unclear. In this study, we explore the role of <i>Drosophila</i> PRL (dPRL) in photoreceptor cell development. We reveal that dPRL, requiring a C-terminal prenylation motif, is highly enriched in the apical membrane of developing photoreceptor cells. Moreover, <i>dPRL</i> knockdown during retinal development results in adult <i>Drosophila</i> retinal degeneration, caused by <i>hid</i>-induced apoptosis. <i>dPRL</i> depletion also mislocalizes cell adhesion and polarity proteins like Armadillo, Crumbs, and DaPKC and relocates the basolateral protein, alpha subunit of Na⁺/K⁺-ATPase, to the presumed apical membrane. Importantly, this polarity disruption is not secondary to apoptosis, as suppressing <i>hid</i> expression does not rescue the polarity defect in <i>dPRL</i>-depleted photoreceptor cells. These findings underscore dPRL’s crucial role in photoreceptor cell polarity and emphasize PRL’s importance in establishing epithelial polarity and maintaining cell survival during retinal development, offering new insights into PRL’s role in normal epithelium.