Document Type

Article

Language

eng

Format of Original

11 p.

Publication Date

2-2004

Publisher

American Society for Microbiology

Source Publication

Eukaryotic Cell

Source ISSN

1535-9778

Original Item ID

doi:10.1128/EC.3.1.72-81.2004; PubMed Central, PMCID: PMC329519

Abstract

Genetic and morphological studies have revealed that the radial spokes regulate ciliary and flagellar bending. Functional and biochemical analysis and the discovery of calmodulin in the radial spokes suggest that the regulatory mechanism involves control of axonemal protein phosphorylation and calcium binding to spoke proteins. To identify potential regulatory proteins in the radial spoke, in-gel kinase assays were performed on isolated axonemes and radial spoke fractions. The results indicated that radial spoke protein 2 (RSP2) can bind ATP and transfer phosphate in vitro. RSP2 was cloned and mapped to the PF24 locus, a gene required for motility. Sequencing revealed that pf24 contains a point mutation converting the first ATG to ATA, resulting in only trace amounts of RSP2 and confirming the RSP2 mapping. Surprisingly, the sequence does not include signature domains for conventional kinases, indicating that RSP2 may not perform as a protein kinase in vivo. However, the predicted RSP2 protein sequence contains Ca2+-dependent calmodulin binding motifs and a GAF domain, a domain found in diverse signaling proteins for binding small ligands including cyclic nucleotides. As predicted from the sequence, recombinant RSP2 binds calmodulin in a calcium-dependent manner. We postulate that RSP2 is a regulatory subunit of the radial spoke involved in localization of calmodulin for control of motility.

Comments

Published version. Eukaryotic Cell, Vol. 3, No. 1 (February 2004): 72-81. DOI. © American Society for Microbiology 2004. Used with permission.

Included in

Biology Commons

Share

COinS