The PP2C Alphabet Is a Negative Regulator of Stress-Activated Protein Kinase Signaling in Drosophila

被引:25
作者
Baril, Caroline [1 ,3 ]
Sahmi, Malha [1 ]
Ashton-Beaucage, Dariel [1 ]
Stronach, Beth [4 ]
Therrien, Marc [1 ,2 ,3 ]
机构
[1] Univ Montreal, Lab Intracellular Signaling, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Dept Pathol & Biol Cellulaire, Montreal, PQ H3C 3J7, Canada
[3] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[4] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
基金
美国国家卫生研究院; 加拿大创新基金会;
关键词
DORSAL CLOSURE; LINEAGE KINASE; CELL-DEATH; B-RAF; JNK; PATHWAY; PHOSPHATASE; SURVIVAL; TRANSDUCTION; RESPONSES;
D O I
10.1534/genetics.108.096461
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Jun N-terminal kinase and 1338 pathways, also known as stress-activated protein kinase (SAPK) pathways, are signaling conduits reiteratively used throughout the development and adult life of metazoans where they play central roles in the control of apoptosis, immune function, and environmental stress responses. We recently identified a Drosophila Ser/Thr phosphatase of the PP2C family, named Alphabet (Alph), which acts as a negative regulator of the Ras/ERK pathway. Here we show that Alph also plays an inhibitory role with respect to Drosophila SAPK signaling during development as well as under stress conditions such as oxidative or genotoxic stresses. Epistasis experiments suggest that Alph acts at a Step upstream of the MAPKKs Hep and Lic. Consistent with this interpretation, biochemical experiments identify the upstream MAPKKKs Slpr, Tak1, and Wnd as putative substrates. Together with previous findings, this work identifies Alph as a general attenuator of MAPK signaling in Drosophila.
引用
收藏
页码:567 / 579
页数:13
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