TY - JOUR
T1 - Planar cell polarity acts through septins to control collective cell movement and ciliogenesis
AU - Kim, Su Kyoung
AU - Shindo, Asako
AU - Park, Tae Joo
AU - Oh, Edwin C.
AU - Ghosh, Srimoyee
AU - Gray, Ryan S.
AU - Lewis, Richard A.
AU - Johnson, Colin A.
AU - Attie-Bittach, Tania
AU - Katsanis, Elias Nicholas
AU - Wallingford, John B.
PY - 2010/9/10
Y1 - 2010/9/10
N2 - The planar cell polarity (PCP) signaling pathway governs collective cell movements during vertebrate embryogenesis, and certain PCP proteins are also implicated in the assembly of cilia. The septins are cytoskeletal proteins controlling behaviors such as cell division and migration. Here, we identified control of septin localization by the PCP protein Fritz as a crucial control point for both collective cell movement and ciliogenesis in Xenopus embryos. We also linked mutations in human Fritz to Bardet-Biedl and Meckel-Gruber syndromes, a notable link given that other genes mutated in these syndromes also influence collective cell movement and ciliogenesis. These findings shed light on the mechanisms by which fundamental cellular machinery, such as the cytoskeleton, is regulated during embryonic development and human disease.
AB - The planar cell polarity (PCP) signaling pathway governs collective cell movements during vertebrate embryogenesis, and certain PCP proteins are also implicated in the assembly of cilia. The septins are cytoskeletal proteins controlling behaviors such as cell division and migration. Here, we identified control of septin localization by the PCP protein Fritz as a crucial control point for both collective cell movement and ciliogenesis in Xenopus embryos. We also linked mutations in human Fritz to Bardet-Biedl and Meckel-Gruber syndromes, a notable link given that other genes mutated in these syndromes also influence collective cell movement and ciliogenesis. These findings shed light on the mechanisms by which fundamental cellular machinery, such as the cytoskeleton, is regulated during embryonic development and human disease.
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UR - http://www.scopus.com/inward/citedby.url?scp=77956505731&partnerID=8YFLogxK
U2 - 10.1126/science.1191184
DO - 10.1126/science.1191184
M3 - Article
C2 - 20671153
AN - SCOPUS:77956505731
SN - 0036-8075
VL - 329
SP - 1337
EP - 1340
JO - Science
JF - Science
IS - 5997
ER -