Phospho-regulation of kinetochore-microtubule attachments by the aurora kinase Ipl1p

The Aurora kinase lpL1p plays a crucial role in regulating kinetochore-microtubule attachments in budding yeast, but the underlying basis for this regulation is not known. To identify IpI1p targets, we first purified 28 kinetochore proteins from yeast protein extracts. These studies identified five previously uncharacterized kinetochore proteins and defined two additional kinetochore subcomplexes. We then used mass spectrometry to identify 18 phosphorylation sites in 7 of these 28 proteins. Ten of these phosphorylation sites are targeted directly by lpL1p, allowing us to identify a consensus phosphorylation site for an Aurora kinase. Our systematic mutational analysis of the IpI1p phosphorylation sites demonstrated that the essential microtubule binding protein Dam1p is a key IpI1p target for regulating kinetochore-microtubule attachments in vivo.