Global Analysis of Cdk1 Substrate Phosphorylation Sites Provides Insights into Evolution
University of California, San Francisco · Harvard University
Abstract
To explore the mechanisms and evolution of cell-cycle control, we analyzed the position and conservation of large numbers of phosphorylation sites for the cyclin-dependent kinase Cdk1 in the budding yeast Saccharomyces cerevisiae. We combined specific chemical inhibition of Cdk1 with quantitative mass spectrometry to identify the positions of 547 phosphorylation sites on 308 Cdk1 substrates in vivo. Comparisons of these substrates with orthologs throughout the ascomycete lineage revealed that the position of most phosphorylation sites is not conserved in evolution; instead, clusters of sites shift position in rapidly evolving disordered regions. We propose that the regulation of protein function by…
Citation impact
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Authors
6Topics & keywords
- Cyclin-dependent kinase 1
- Phosphorylation
- Protein phosphorylation
- Saccharomyces cerevisiae
- Biology
- Kinase
- Cell biology
- Protein kinase A
- Life in Land