ODF1 Phosphorylation by Cdk5/p35 Enhances ODF1-OIP1 Interaction

Cdk5 and p35 are integral components of the sperm tail outer dense fibers (ODFs), which contribute to the distinct morphology and function of the sperm tail. In this study, we sought to characterize and investigate the significance of Cdk5/p35 association with ODFs. We show that ODF2 interacts with Cdk5 and p35 but not with the Cdk5/p35 heterodimer. By using deletion mutants, the ODF2 binding region in p35 was mapped to residues 122 to 198. This overlaps the Cdk5 binding region in p35, explaining the inability of ODF2 to bind to the Cdk5/p35 complex. In vitro phosphorylation assay showed that although Cdk5/p35 does not phosphorylate ODF2, it phosphorylates ODF1. Mass spectrometry revealed that Cdk5/p35 specifically phosphorylates Ser193 in the ODF1 C-terminal region containing the Cys-X-Pro motif, the interaction site for the novel RING finger protein, ODF1 interacting protein (OIP1), a candidate E3 ubiquitin ligase, that also localizes in the sperm tail. Cdk5 phosphorylation of ODF1 Ser193 results in enhanced ODF1-OIP1 interaction. These findings suggest that Cdk5 may be important in promoting ODF1 degradation, and potentially, the detachment and fragmentation of the sperm tail following fertilization.

[1]  J. Rosales,et al.  Extraneuronal roles of cyclin‐dependent kinase 5 , 2006, BioEssays : news and reviews in molecular, cellular and developmental biology.

[2]  K. Mikoshiba,et al.  Cdk5-dependent regulation of glucose-stimulated insulin secretion , 2005, Nature Medicine.

[3]  Gordon Broderick,et al.  Localization, Annotation, and Comparison of the Escherichia coli K-12 Proteome under Two States of Growth*S , 2005, Molecular & Cellular Proteomics.

[4]  J. Ernst,et al.  GTP-dependent Secretion from Neutrophils Is Regulated by Cdk5* , 2004, Journal of Biological Chemistry.

[5]  K. Sarker,et al.  L6 myoblast differentiation is modulated by Cdk5 via the PI3K–AKT–p70S6K signaling pathway , 2004, Oncogene.

[6]  R. Oko,et al.  Outer Dense Fibers Serve as a Functional Target for Cdk5·p35 in the Developing Sperm Tail* , 2004, Journal of Biological Chemistry.

[7]  F. A. van der Hoorn,et al.  Novel RING Finger Protein OIP1 Binds to Conserved Amino Acid Repeats in Sperm Tail Protein ODF11 , 2003, Biology of reproduction.

[8]  S. Nagdas,et al.  Identification of Ras and Its Downstream Signaling Elements and Their Potential Role in Hamster Sperm Motility1 , 2002, Biology of reproduction.

[9]  Li-Huei Tsai,et al.  A decade of CDK5 , 2001, Nature Reviews Molecular Cell Biology.

[10]  P. Berggren,et al.  Cyclin-dependent Kinase 5 Promotes Insulin Exocytosis* , 2001, The Journal of Biological Chemistry.

[11]  L. Tsai,et al.  Structure and Regulation of the CDK5-p25nck5a Complex , 2001 .

[12]  K. Y. Lee,et al.  Purification of dual-tagged intact recombinant proteins. , 2000, Biochemical and biophysical research communications.

[13]  M. O’Bryan,et al.  Isolation and characterization of rat sperm tail outer dense fibres and comparison with rabbit and human spermatozoa using a polyclonal antiserum. , 1999, Journal of reproduction and fertility.

[14]  Mingjie Zhang,et al.  Identification and Structure Characterization of a Cdk Inhibitory Peptide Derived from Neuronal-specific Cdk5 Activator* , 1999, The Journal of Biological Chemistry.

[15]  J. H. Wang,et al.  Neuronal Cdc2-like kinases: neuron-specific forms of Cdk5. , 1997, The international journal of biochemistry & cell biology.

[16]  L. Tsai,et al.  The role of cyclin-dependent kinase 5 and a novel regulatory subunit in regulating muscle differentiation and patterning. , 1997, Genes & development.

[17]  M. Kitzmann,et al.  Cyclin dependent kinase 5, cdk5, is a positive regulator of myogenesis in mouse C2 cells. , 1997, Journal of cell science.

[18]  Mingjie Zhang,et al.  Cyclin-dependent Kinase 5 (Cdk5) Activation Domain of Neuronal Cdk5 Activator , 1997, The Journal of Biological Chemistry.

[19]  R. Oko,et al.  Interactional Cloning of the 84-kDa Major Outer Dense Fiber Protein Odf84 , 1997, The Journal of Biological Chemistry.

[20]  T. Hunter,et al.  Identification of Functional Domains in the Neuronal Cdk5 Activator Protein* , 1997, The Journal of Biological Chemistry.

[21]  F. A. van der Hoorn,et al.  Self-interaction of the major 27-kilodalton outer dense fiber protein is in part mediated by a leucine zipper domain in the rat. , 1996, Biology of reproduction.

[22]  Jerry H. Wang,et al.  Interaction of Cyclin-dependent Kinase 5 (Cdk5) and Neuronal Cdk5 Activator in Bovine Brain (*) , 1996, The Journal of Biological Chemistry.

[23]  R. Cone,et al.  Dense fibers protect mammalian sperm against damage. , 1990, Biology of reproduction.

[24]  C. Gagnon Controls of Sperm Motility: Biological and Clinical Aspects , 1990 .

[25]  R. Oko Comparative analysis of proteins from the fibrous sheath and outer dense fibers of rat spermatozoa. , 1988, Biology of reproduction.

[26]  M. Brito,et al.  Polypeptide composition of rat sperm outer dense fibers. A simple procedure to isolate the fibrillar complex. , 1984, The Journal of biological chemistry.

[27]  L. Tsai,et al.  Structure and regulation of the CDK5-p25(nck5a) complex. , 2001, Molecular cell.

[28]  Mingjie Zhang,et al.  Cyclin-dependent Kinase 5 ( Cdk 5 ) Activation Domain of Neuronal Cdk 5 Activator EVIDENCE OF THE EXISTENCE OF CYCLIN FOLD IN NEURONAL Cdk 5 a ACTIVATOR , 1997 .

[29]  C. Lindemann Functional significance of the outer dense fibers of mammalian sperm examined by computer simulations with the geometric clutch model. , 1996, Cell motility and the cytoskeleton.

[30]  C. Brokaw,et al.  Multiple protein kinase activities required for activation of sperm flagellar motility. , 1995, Cell motility and the cytoskeleton.