Mammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypes

Maria E. Teves, David R. Nagarkatti-Gude, Zhibing Zhang, Jerome F. Strauss

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

The axoneme genes, their encoded proteins, their functions and the structures they form are largely conserved across species. Much of our knowledge of the function and structure of axoneme proteins in cilia and flagella is derived from studies on model organisms like the green algae, Chlamydomonas reinhardtii. The core structure of cilia and flagella is the axoneme, which in most motile cilia and flagella contains a 9+2 configuration of microtubules. The two central microtubules are the scaffold of the central pair complex (CPC). Mutations that disrupt CPC genes in Chlamydomonas and other model organisms result in defects in assembly, stability and function of the axoneme, leading to flagellar motility defects. However, targeted mutations generated in mice in the orthologous CPC genes have revealed significant differences in phenotypes of mutants compared to Chlamydomonas. Here we review observations that support the concept of cell-type specific roles for the CPC genes in mice, and an expanded repertoire of functions for the products of these genes in cilia, including non-motile cilia, and other microtubule-associated cellular functions.

Original languageEnglish (US)
Pages (from-to)3-22
Number of pages20
JournalCytoskeleton
Volume73
Issue number1
DOIs
StatePublished - Jan 1 2016
Externally publishedYes

Keywords

  • Axoneme
  • Central pair complex
  • Cilia
  • Flagella

ASJC Scopus subject areas

  • Structural Biology
  • Cell Biology

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