HCLK2 is required for activity of the DNA damage response kinase ATR
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HCLK2 is required for activity of the DNA damage response kinase ATR. / Rendtlew Danielsen, Jannie M; Larsen, Dorthe Helena; Schou, Kenneth Bødtker; Freire, Raimundo; Falck, Jacob; Bartek, Jiri; Lukas, Jiri.
In: Journal of Biological Chemistry, Vol. 284, No. 7, 2008, p. 4140-7.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - HCLK2 is required for activity of the DNA damage response kinase ATR
AU - Rendtlew Danielsen, Jannie M
AU - Larsen, Dorthe Helena
AU - Schou, Kenneth Bødtker
AU - Freire, Raimundo
AU - Falck, Jacob
AU - Bartek, Jiri
AU - Lukas, Jiri
N1 - Keywords: Carrier Proteins; Cell Cycle Proteins; Chromosomal Proteins, Non-Histone; DNA Damage; DNA-Binding Proteins; Enzyme Induction; Enzyme Stability; Hela Cells; Humans; Nuclear Proteins; Protein Kinases; Protein-Serine-Threonine Kinases; Protein-Tyrosine Kinases
PY - 2008
Y1 - 2008
N2 - ATR is a protein kinase that orchestrates the cellular response to replication problems and DNA damage. HCLK2 has previously been reported to stabilize ATR and Chk1. Here we provide evidence that human HCLK2 acts at an early step in the ATR signaling pathway and contributes to full-scale activation of ATR kinase activity. We show that HCLK2 forms a complex with ATR-ATRIP and the ATR activator TopBP1. We demonstrate that HCLK2-induced ATR kinase activity toward substrates requires TopBP1 and vice versa and provides evidence that HCLK2 facilitates efficient ATR-TopBP1 association. Consistent with its role in ATR activation, HCLK2 depletion severely impaired phosphorylation of multiple ATR targets including Chk1, Nbs1, and Smc1 after DNA damage. We show that HCLK2 is required for and stimulates ATR autophosphorylation and activity toward different substrates in vitro. Furthermore, HCLK2 depletion abrogated the G(2) checkpoint and decreased survival of cells after exposure to DNA damaging agents and replicative stress. Overall, our data suggest that HCLK2 facilitates ATR activation and, therefore, contributes to ATR-mediated checkpoint signaling. Importantly, our results suggest that HCLK2 functions in the same pathway as TopBP1 but that the two proteins regulate different steps in ATR activation.
AB - ATR is a protein kinase that orchestrates the cellular response to replication problems and DNA damage. HCLK2 has previously been reported to stabilize ATR and Chk1. Here we provide evidence that human HCLK2 acts at an early step in the ATR signaling pathway and contributes to full-scale activation of ATR kinase activity. We show that HCLK2 forms a complex with ATR-ATRIP and the ATR activator TopBP1. We demonstrate that HCLK2-induced ATR kinase activity toward substrates requires TopBP1 and vice versa and provides evidence that HCLK2 facilitates efficient ATR-TopBP1 association. Consistent with its role in ATR activation, HCLK2 depletion severely impaired phosphorylation of multiple ATR targets including Chk1, Nbs1, and Smc1 after DNA damage. We show that HCLK2 is required for and stimulates ATR autophosphorylation and activity toward different substrates in vitro. Furthermore, HCLK2 depletion abrogated the G(2) checkpoint and decreased survival of cells after exposure to DNA damaging agents and replicative stress. Overall, our data suggest that HCLK2 facilitates ATR activation and, therefore, contributes to ATR-mediated checkpoint signaling. Importantly, our results suggest that HCLK2 functions in the same pathway as TopBP1 but that the two proteins regulate different steps in ATR activation.
U2 - 10.1074/jbc.M808174200
DO - 10.1074/jbc.M808174200
M3 - Journal article
C2 - 19097996
VL - 284
SP - 4140
EP - 4147
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
SN - 0021-9258
IS - 7
ER -
ID: 18698049