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Garcia-Baudino, C.

Publications and source records attributed to Garcia-Baudino, C..

2 recordsLinked to original sources

Sox2 Regulates Lateral Line Morphogenesis via Yap/Taz-MediatedMechanotransduction

Organ morphogenesis relies on a tightly regulated interplay between cell proliferation, migration, and differentiation. Emerging evidence suggests that mechanical forces act alongside molecular signals to orchestrate tissue patterning, yet how these diverse inputs are integrated remains poorly understood. The zebrafish posterior lateral line offers a powerful in vivo model for studying how cellular behaviors and mechanosensitive signaling are spatiotemporally coordinated during organogenesis. Here, we identify the transcription factor Sox2 as a key regulator of lateral line morphogenesis, influencing the positioning, size, and number of neuromasts, the sensory organs of the lateral line. Loss of Sox2 leads to increased lateral line primordium cell proliferation, disrupted ZO1 deposition at the rosettes and smaller neuromasts positioned more posteriorly along the body axis, while Sox2 overexpression produces opposite phenotypes. Sox2 functions in part by repressing Yap/Taz(Wwtr1) signaling in the primordium. Reduced Yap/Taz activity results in more anterior neuromast deposition and premature termination of primordium migration. Furthermore, we show that as the primordium expands through cell-proliferation, increased cell-junction tension activates Yap/Taz, thereby influencing lateral line development. Reducing overproliferation in sox2-/-embryos diminishes the elevated Yap/Taz activity, supporting a model in which Sox2 limits proliferation to suppress Yap/Taz signaling and ensure proper primordium morphogenesis. These findings show that Sox2, together with the related SoxB1 transcription factor Sox3, regulates lateral line morphogenesis by coordinating primordium proliferation, neuromast size, and Yap/Taz-dependent mechanosensitive signaling.

developmental biology↗

DET1-mediated COP1 regulation avoids HY5 activity over second-site targets to tune plant photomorphogenesis

DE-ETIOLATED1 (DET1) is a negative regulator of plant photomorphogenesis acting as a component of the C3D complex, which can further associate to CULLIN4 to form a CRL4C3D E3 ubiquitin ligase. CRL4C3D is thought to act together with CRL4COP1SPA ubiquitin ligase, to promote the ubiquitin-mediated degradation of the master regulatory transcription factor ELONGATED HYPOCOTYL5 (HY5), thereby controlling photomorphogenic gene regulatory networks. Yet, functional links between COP1 and DET1 have long remained elusive. Here, upon mass spectrometry identification of DET1 and COP1-associated proteins, we provide in vivo evidence that DET1 associates with COP1 to promote its destabilization, a process necessary to dampen HY5 protein abundance. By regulating HY5 over-accumulation, DET1 is critical to avoid its association to second-site loci, including many PIF3 target genes. Accordingly, excessive HY5 levels result in an increased HY5 repressive activity and are sufficient to trigger fusca-like phenotypes otherwise observed typically in COP1 and COP9 signalosome mutant seedlings. This study therefore identifies that DET1-mediated regulation of COP1 stability tunes down HY5 cistrome and avoids hyper-photomorphogenic responses that might compromise plant viability.

plant biology↗