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bioRxiv · 10.1101/2023.01.11.523641

Not all Notch pathway mutations are equal in the embryonic mouse retina

Bosze, B.·Suarez-Navarro, J.·Cajias, I.·Brzezinski, J. A.·Brown, N. L.
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Abstract

In the vertebrate retina, combinations of Notch ligands, receptors, and ternary complex components determine the destiny of retinal progenitor cells by regulating Hes effector gene activity. Owing to reiterated Notch signaling in numerous tissues throughout development, there are multiple vertebrate paralogues for nearly every node in this pathway. These Notch signaling components can act redundantly or in a compensatory fashion during development. To dissect the complexity of this pathway during retinal development, we used seven germline or conditional mutant mice and two spatiotemporally distinct Cre drivers. We perturbed the Notch ternary complex and multiple Hes genes with two overt goals in mind. First, we wished to determine if Notch signaling is required in the optic stalk/nerve head for Hes1 sustained expression and activity. Second, we aimed to test if Hes1, 3 and 5 genes are functionally redundant during early retinal histogenesis. With our allelic series, we found that disrupting Notch signaling consistently blocked mitotic growth and overproduced ganglion cells, but we also identified two significant branchpoints for this pathway. In the optic stalk/nerve head, sustained Hes1 is regulated independent of Notch signaling, whereas during photoreceptor genesis both Notch-dependent and -independent roles for Rbpj and Hes1 impact photoreceptor genesis in opposing manners.

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Bosze, B., Suarez-Navarro, J., Cajias, I., Brzezinski, J. A., Brown, N. L.. 2023-01-12. Not all Notch pathway mutations are equal in the embryonic mouse retina. https://doi.org/10.1101/2023.01.11.523641

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