Chlamydomonas IFT88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg737, Are Required for Assembly of Cilia and Flagella

Author:

Pazour Gregory J.1,Dickert Bethany L.1,Vucica Yvonne2,Seeley E. Scott2,Rosenbaum Joel L.2,Witman George B.1,Cole Douglas G.3

Affiliation:

1. Department of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01655

2. Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520

3. Department of Microbiology, Molecular Biology, and Biochemistry, University of Idaho, Moscow, Idaho 83844

Abstract

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

Reference63 articles.

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