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The Chloroplast Calcium Sensor CAS Is Required for Photoacclimation in Chlamydomonas reinhardtii
被引:120
作者:
Petroutsos, Dimitris
[1
]
Busch, Andreas
[1
]
Janssen, Ingrid
[1
]
Trompelt, Kerstin
[1
]
Bergner, Sonja Verena
[1
]
Weinl, Stefan
[1
]
Holtkamp, Michael
[2
]
Karst, Uwe
[2
]
Kudla, Joerg
[1
]
Hippler, Michael
[1
]
机构:
[1] Univ Munster, Inst Plant Biol & Biotechnol, D-48143 Munster, Germany
[2] Univ Munster, Inst Inorgan & Analyt Chem, D-48149 Munster, Germany
来源:
关键词:
PLASMA EMISSION-SPECTROMETRY;
MEASURING DETECTION LIMITS;
CYTOSOLIC CA2+ TRANSIENTS;
PHOTOSYSTEM-II;
THYLAKOID MEMBRANE;
BIOENERGETIC PATHWAYS;
ARABIDOPSIS-THALIANA;
ARTIFICIAL MICRORNAS;
FLAGELLAR EXCISION;
CALMODULIN-BINDING;
D O I:
10.1105/tpc.111.087973
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The plant-specific calcium binding protein CAS (calcium sensor) has been localized in chloroplast thylakoid membranes of vascular plants and green algae. To elucidate the function of CAS in Chlamydomonas reinhardtii, we generated and analyzed eight independent CAS knockdown C. reinhardtii lines (cas-kd). Upon transfer to high-light (HL) growth conditions, cas-kd lines were unable to properly induce the expression of LHCSR3 protein that is crucial for nonphotochemical quenching. Prolonged exposure to HL revealed a severe light sensitivity of cas-kd lines and caused diminished activity and recovery of photosystem II (PSII). Remarkably, the induction of LHCSR3, the growth of cas-kd lines under HL, and the performance of PSII were fully rescued by increasing the calcium concentration in the growth media. Moreover, perturbing cellular Ca2+ homeostasis by application of the calmodulin antagonist W7 or the G-protein activator mastoparan impaired the induction of LHCSR3 expression in a concentration-dependent manner. Our findings demonstrate that CAS and Ca2+ are critically involved in the regulation of the HL response and particularly in the control of LHCSR3 expression.
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页码:2950 / 2963
页数:14
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