#centrosome-directed
Alström syndrome is a #cilia-related disorder caused by loss of ALMS1, a proximal #centriole protein. Thao P. Phan et al. @reitergroup.bsky.social show that ALMS1 protects centriole integrity to enable #centrosome-directed trafficking during cilia formation & maintenance rupress.org/jcb/article/...
November 2, 2026 at 6:01 PM
Alström syndrome is a cilia-related disorder caused by loss of ALMS1, a proximal centriole protein. In @jcb.org, Phan et al @reitergroup.bsky.social show that ALMS1 protects centriole integrity to enable centrosome-directed trafficking during cilia formation & maintenance rupress.org/jcb/article/...
November 2, 2026 at 6:00 PM
PCM1 enriched at the mother centrosome directs posterior movement of Notch ligand–containing endosomes; loss of PCM1 increases neuron production over progenitors, revealing a centrosome-to-endosome link in… https://basebybase.castos.com/episodes/pcm1-centrosome-endosome-asymmetry
249: PCM1 links centrosome asymmetry to endosome dynamics
️ Episode 249: PCM1 links centrosome asymmetry to endosome dynamics In this episode of PaperCast Base by Base, we explore In developing neural progenitors PCM1 localizes to the mother centrosome and to Notch ligand-containing endosomes, promoting Par-3/dynein assembly and Rab5-to-Rab11 trafficking to bias posterior-directed endosome segregation and preserve progenitor fate Study Highlights:Pcm1 is asymmetrically enriched at the posterior mother centrosome (Cep83+) in zebrafish radial glia progenitors and is also found on central-zone Notch ligand (Dld)-containing endosomes. In vivo time-lapse imaging and expansion microscopy show Pcm1 puncta move with Dld endosomes and promote posterior-directed polarized dynamics. Loss of pcm1 disrupts Rab5b-to-Rab11a trafficking, reduces Par-3 and dynein co-assembly on recycling endosomes, lowers Notch signaling, and shifts divisions toward neuron–neuron outcomes at the expense of progenitors. Similar PCM1–PARD3–CEP83–RAB11 associations and asymmetr…
basebybase.castos.com
January 5, 2026 at 12:01 AM