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Distinct #Cdc42 protein levels differentially regulate polarized growth and cell fusion in Schizosaccharomyces pombe

The work of @sajjitasaha.bsky.social and @aiswaryasajeevan.bsky.social, with Laura Merlini and Vincent Vincenzetti, now out in @plosbiology.org !

@biology-unige.bsky.social

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Oligomerization-dependent and synergistic regulation of Cdc42 GTPase cycling by a GEF and a GAP - EMBO Reports Cell polarity is a crucial biological process essential for cell division, directed growth, and motility. In Saccharomyces cerevisiae, polarity establishment centers around the small Rho-type GTPase C...

New paper out in EMBO Reports!
We show that Cdc42 regulation is oligomerization-dependent and that a GEF and a GAP act synergistically: Cdc24 relieves self-inhibition of oligomeric Rga2, enabling robust Cdc42 cycling.
doi.org/10.1038/s44319-026-00695-7
#cellpolarity #Cdc42 #synergy #syntheticbiology

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CDC42‐Effector Proteins Regulate Higher Order Structure of Septins Required for CNS Myelin Integrity CDC42-effector proteins 1/2 are present in CNS myelin. They facilitate the higher order structure of myelin septin filaments. Their loss impairs septin-dependent scaffolding of myelin. Myelin o...

If you're interested in the factors that enable the regular structure of CNS #myelin sheaths by #oligodendrocytes, check this out. Featuring a #CDC42 - effector proteins - #septin axis. Congrats to 1st author Sophie, and a big thank you to all who contributed

onlinelibrary.wiley.com/doi/10.1002/...

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BOO‑associated #BladderFibrosis is driven by #EMT‑linked cytoskeletal remodeling via the TGF‑β/Cdc42/Cdc42ep1/F‑actin/Fibronectin axis; #Cdc42 inhibition suppresses #fibrosis, highlighting cytoskeletal regulators as therapeutic targets.

#OpenAccess: doi.org/10.1016/j.ge...

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Dr Honorine Ward highlights Adam Sateriale & colleagues’ @cp-cellhostmicrobe.bsky.social article on a #virulence factor, #Cryptosporidium #MVP1, modulating #intestinal #microvilli by interacting with host #EBP50 & #CDC42. @tuftsmedicalcenter.bsky.social

authors.elsevier.com/a/1lH505Eb1x...

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Cdc42 deletion yielded enamel defects by disrupting mitochondria and producing reactive oxygen species in dental epithelium

Cdc42 deletion yielded enamel defects by disrupting mitochondria and producing reactive oxygen species in dental epithelium

This study demonstrates the multidimensional and pivotal role that #Cdc42 plays in #enamel development and #ToothRepair, using inducible epithelium-specific knockout Cdc42 mice, and underscores its part in #Ameloblast differentiation and enamel matrix formation. #medsky

#OpenAccess: buff.ly/lJePLwg

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