Different Signaling and Cell Death Roles of Heterotrimeric G Protein α and β Subunits in the Arabidopsis Oxidative Stress Response to Ozone

Различные роли субъединиц α и β гетеротримерного G-белка в сигнализации и гибели клеток при оксидативном стрессе Arabidopsis в ответ на озон
Nina V. Fedoroff, Shiyu Wang, Alan M. Jones, Jin‐Gui Chen, Jung-Hee Joo
2005-02-11

Arabidopsis oxidative burstAtrbohD and AtrbohF NADPH oxidaseschloroplast-derived reactive oxygen species (ROS)heterotrimeric G protein alpha subunit (Galpha)heterotrimeric G protein beta subunit (Gbeta)
Arabidopsis thaliana plants with null mutations in the genes encoding the alpha and beta subunits of the single heterotrimeric G protein are less and more sensitive, respectively, to O3 damage than wild-type Columbia-0 plants. The first peak of the bimodal oxidative burst elicited by O3 in wild-type plants is almost entirely missing in both mutants. The late peak is normal in plants lacking the Gbeta protein but missing in plants lacking the Galpha protein. Endogenous reactive oxygen species (ROS) are first detectable in chloroplasts of leaf epidermal guard cells. ROS production in adjacent cells is triggered by extracellular ROS signals produced by guard cell membrane-associated NADPH oxidases encoded by the AtrbohD and AtrbohF genes. The late, tissue damage-associated component of the oxidative burst requires only the Galpha protein and arises from multiple cellular sources. The early component of the oxidative burst, arising primarily from chloroplasts, requires signaling through the heterotrimer (or the Gbetagamma complex) and is separable from Galpha-mediated activation of membrane-bound NADPH oxidases necessary for both intercellular signaling and cell death.
1
Endogenous ROS are first detectable in chloroplasts of leaf epidermal guard cells.
2
Null mutation in Gα reduces sensitivity to ozone damage compared to wild-type Columbia-0.
3
Null mutation in Gβ increases sensitivity to ozone damage compared to wild-type Columbia-0.
4
ROS production in adjacent cells is triggered by extracellular ROS from guard cell membrane-associated NADPH oxidases encoded by AtrbohD and AtrbohF.
5
The early oxidative burst, primarily from chloroplasts, requires signaling through the heterotrimer (or Gβγ) and is separable from Gα-mediated activation of membrane NADPH oxidases required for intercellular signaling and cell death.
6
The early peak of the bimodal oxidative burst induced by O3 is almost entirely missing in both Gα and Gβ mutants.
7
The late oxidative burst peak is absent in Gα mutants but normal in Gβ mutants.
8
The late, tissue-damage-associated oxidative burst requires only Gα and originates from multiple cellular sources.

Heterotrimeric G protein α and β subunits in Arabidopsis thaliana during ozone-induced oxidative stress

Their distinct signaling roles in regulating the biphasic oxidative burst (early chloroplast-derived ROS and late tissue-damage-associated ROS), intercellular ROS signaling via NADPH oxidases (AtrbohD/AtrbohF), and resultant cell death sensitivity

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2005-02-11
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Nina V. Fedoroff
Shiyu Wang
Alan M. Jones
Jin‐Gui Chen
Jung-Hee Joo
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