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Angueyra, J.

Publications and source records attributed to Angueyra, J..

2 recordsLinked to original sources

Neurexin 3 is required for the specific S-cone to S-cone bipolar cell synapse in the mammalian retina

Precise wiring within sensory systems is critical for the accurate transmission of information. In the visual system, S-cone photoreceptors specialize in detecting short-wavelength light, crucial to color perception and environmental cue detection. S-cones form specific synapses with S-cone bipolar cells (SCBCs), a connection that is remarkably consistent across species. Yet, the molecular mechanisms guiding this specificity remain unexplored. To address this, we used the cone-dominant ground squirrel for deep-sequencing of cone subtype transcriptomes and identified Nrxn3 as an essential molecule for the S-cone to SCBC synapse. Using transgenic mouse models, we further examined the role of Nrxn3 in S-cones and discovered a significant reduction of SCBC connections in the absence of Nrxn3. This finding extends the known functions of neurexins, typically associated with synapse regulation, by highlighting their essential role in a specific synaptic connection for the first time. Moreover, the differentially expressed genes identified here pave the way for further investigations into the unique functions of cone subtypes.

neuroscience↗

Identification of transcription factors involved in the specification of photoreceptor subtypes

During development, retinal progenitors navigate a complex landscape of fate decisions that results in the generation of unique cell types necessary for proper vision. Here, we aim to provide the resources and techniques required to identify fac-tors that are critical for fate decisions in photoreceptors. These factors help create a diversity of photoreceptor subtypes that sustain vision in day and night, enable the discrimination of colors, facilitate the detection of prey and predators, and support other aspects of vision. First, we generate a key resource: a high-quality and deep transcriptomic profile of each photoreceptor subtype in zebrafish. We make this resource openly accessible, easy to explore and integrate it with other currently available photoreceptor transcriptomic datasets. Second, using our transcriptomic profiles, we derive an in-depth map of expression of transcription factors in photoreceptors--potential key players in cell-fate decisions. Third, we explore CRISPR-FO screening as a fast, efficient and versatile technique to assess the involvement of candidate transcription factors in photoreceptor subtype-specification. We first show that known phenotypes can be easily replicated: loss of S cones in foxq2 mutants and loss of rods in nr2e3 mutants. We then explore four additional transcription factors of unknown function (Skor1a, Sall1a, Lrrfip1a and Xbp1) and find no evidence for their involvement in photoreceptor-subtype specification. Finally, we identify novel functions of Tbx2, demonstrating that it plays a central role in controlling the identity of all photoreceptor sub-types within the retina. Our study provides an open roadmap to discover additional factors involved in this process. This dataset and screening method will be a valuable way to explore the genes involved in many essential aspects of photoreceptor biology.

neuroscience↗