Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene Tg737, are required for assembly of cilia and flagella

被引:856
作者
Pazour, GJ
Dickert, BL
Vucica, Y
Seeley, ES
Rosenbaum, JL
Witman, GB
Cole, DG
机构
[1] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[3] Univ Idaho, Dept Microbiol Mol Biol & Biochem, Moscow, ID 83844 USA
关键词
orpk; intraflagellar transport; primary cilia; kinesin-II; cytoplasmic dynein;
D O I
10.1083/jcb.151.3.709
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intraflagellar transport (IFT) is a rapid movement of multi-subunit protein particles along flagellar microtubules and is required for assembly and maintenance of eukaryotic flagella. We cloned and sequenced a Chlamydomonas cDNA encoding the IFT88 subunit of the IFT particle and identified a Chlamydomonas insertional mutant that is missing this gene. The phenotype of this mutant is normal except for the complete absence of flagella, IFT88 is homologous to mouse and human genes called Tg737. Mice with defects in Tg737 die shortly after birth from polycystic kidney disease. We show that the primary cilia in the kidney of Tg737 mutant mice are shorter than normal. This indicates that IFT is important for primary cilia assembly in mammals. It is likely that primary cilia have an important function in the kidney and that defects in their assembly can lead to polycystic kidney disease.
引用
收藏
页码:709 / 718
页数:10
相关论文
共 64 条
  • [1] Afzelius B A, 1979, Int Rev Exp Pathol, V19, P1
  • [2] SCANNING ELECTRON-MICROSCOPIC STUDY OF NEPHRON
    ANDREWS, PM
    PORTER, KR
    [J]. AMERICAN JOURNAL OF ANATOMY, 1974, 140 (01): : 81 - 115
  • [3] BACCETTI B, 1993, ANDROLOGIA, V25, P331
  • [4] Barr MM, 1999, NATURE, V401, P386, DOI 10.1038/43913
  • [5] Beech PL, 1996, J CELL SCI, V109, P889
  • [6] BESHARSE JC, 1989, CILIARY FLAGELLAR ME, P389
  • [7] Blatch GL, 1999, BIOESSAYS, V21, P932, DOI 10.1002/(SICI)1521-1878(199911)21:11<932::AID-BIES5>3.3.CO
  • [8] 2-E
  • [9] POLYCYSTIC DISEASE OF KIDNEYS AND LIVER PRESENTING IN CHILDHOOD
    BLYTH, H
    OCKENDEN, BG
    [J]. JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) : 257 - +
  • [10] Polycystin-L is a calcium-regulated cation channel permeable to calcium ions
    Chen, XZ
    Vassilev, PM
    Basora, N
    Peng, JB
    Nomura, H
    Segal, Y
    Brown, EM
    Reeders, ST
    Hediger, MA
    Zhou, J
    [J]. NATURE, 1999, 401 (6751) : 383 - 386