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Alk1 and Alk2 are two new cell cycle-regulated haspin-Like proteins in budding yeast
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作者:

Nespoli, Alessandro
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

Vercillo, Raffaella
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

di Nola, Lisa
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

Diani, Laura
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

Giannattasio, Michele
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

Plevani, Paolo
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy

Muzi-Falconi, Marco
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Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
机构:
[1] Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
来源:
关键词:
cell cycle control;
mitosis;
protein degradation;
protein phosphorylation;
protein kinase;
D O I:
10.4161/cc.5.13.2914
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Haspin is a protein kinase identified in mouse and human cells, and genes coding for haspin-like proteins are present in virtually all eukaryotic genomes sequenced so far. Two haspin homologues, called Alk1 and Alk2, are present in the yeast Saccharomyces cerevisiae. Both Alk1 and Alk2 exhibit a weak auto-kinase activity in vitro, are phosphoproteins in vivo and are hyperphosphorylated in response to DNA damage. The amount and modification of the two proteins is greatly regulated during the cell cycle. In fact, Alk1 and Alk2 levels peak in mitosis and late-S/G2, respectively, and phosphorylation of both proteins is maximal in mitosis. Control of protein stability plays a major role in Alk2 regulation. The half-life of Alk2 is particularly short in G1; mutagenesis and genetic analysis indicate that its degradation is controlled by the APC pathway. Overexpression of ALK2, but not of ALK1, causes a mitotic arrest, which is correlated to the kinase activity of the protein. This finding, together with its cell cycle regulation, suggests a role for Alk2 in the control of mitosis.
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页码:1464 / 1471
页数:8
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