TY - JOUR
T1 - Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia
AU - Ishikawa, Hiroaki
AU - Kubo, Akiharu
AU - Tsukita, Shoichiro
AU - Tsukita, Sachiko
N1 - Funding Information:
We thank all the members of our laboratory for helpful discussions. We are also grateful to N. Minato and Y. Hamazaki for help with FACS analysis. This work was supported in part by a Grant-in-Aid for Scientific Research (B) to Sa.T. from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2005/5
Y1 - 2005/5
N2 - Outer dense fibre 2 (Odf2; also known as cenexin) was initially identified as a main component of the sperm tail cytoskeleton, but was later shown to be a general scaffold protein that is specifically localized at the distal/subdistal appendages of mother centrioles. Here we show that Odf2 expression is suppressed in mouse F9 cells when both alleles of Odf2 genes are deleted. Unexpectedly, the cell cycle of Odf2-/- cells does not seem to be affected. Immunofluorescence and ultrathin-section electron microscopy reveals that in Odf2-/- cells, distal/subdistal appendages disappear from mother centrioles, making it difficult to distinguish mother from daughter centrioles. In Odf2-/- cells, however, the formation of primary cilia is completely suppressed, although ∼25% of wild-type F9 cells are ciliated under the steady-state cell cycle. The loss of primary cilia in Odf2-/- F9 cells can be rescued by exogenous Odf2 expression. These findings indicate that Odf2 is indispensable for the formation of distal/subdistal appendages and the generation of primary cilia, but not for other cell-cycle-related centriolar functions.
AB - Outer dense fibre 2 (Odf2; also known as cenexin) was initially identified as a main component of the sperm tail cytoskeleton, but was later shown to be a general scaffold protein that is specifically localized at the distal/subdistal appendages of mother centrioles. Here we show that Odf2 expression is suppressed in mouse F9 cells when both alleles of Odf2 genes are deleted. Unexpectedly, the cell cycle of Odf2-/- cells does not seem to be affected. Immunofluorescence and ultrathin-section electron microscopy reveals that in Odf2-/- cells, distal/subdistal appendages disappear from mother centrioles, making it difficult to distinguish mother from daughter centrioles. In Odf2-/- cells, however, the formation of primary cilia is completely suppressed, although ∼25% of wild-type F9 cells are ciliated under the steady-state cell cycle. The loss of primary cilia in Odf2-/- F9 cells can be rescued by exogenous Odf2 expression. These findings indicate that Odf2 is indispensable for the formation of distal/subdistal appendages and the generation of primary cilia, but not for other cell-cycle-related centriolar functions.
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U2 - 10.1038/ncb1251
DO - 10.1038/ncb1251
M3 - Article
C2 - 15852003
AN - SCOPUS:18344396250
SN - 1465-7392
VL - 7
SP - 517
EP - 524
JO - Nature Cell Biology
JF - Nature Cell Biology
IS - 5
ER -