Loss-of-function of OsSTN8 suppresses the photosystem II core protein phosphorylation and interferes with the photosystem II repair mechanism in rice (Oryza sativa)

Krishna Nath, Roshan Sharma Poudyal, Joon Seob Eom, Yu Shin Park, Ismayil S. Zulfugarov, Sujata R. Mishra, Altanzaya Tovuu, Nayeoon Ryoo, Ho Sung Yoon, Hong Gil Nam, Gynheung An, Jong Seong Jeon, Choon Hwan Lee

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

STN8 kinase is involved in photosystem II (PSII) core protein phosphorylation (PCPP). To examine the role of PCPP in PSII repair during high light (HL) illumination, we characterized a T-DNA insertional knockout mutant of the rice (Oryza sativa) STN8 gene. In this osstn8 mutant, PCPP was significantly suppressed, and the grana were thin and elongated. Upon HL illumination, PSII was strongly inactivated in the mutants, but the D1 protein was degraded more slowly than in wild-type, and mobilization of the PSII supercomplexes from the grana to the stromal lamellae for repair was also suppressed. In addition, higher accumulation of reactive oxygen species and preferential oxidation of PSII reaction center core proteins in thylakoid membranes were observed in the mutants during HL illumination. Taken together, our current data show that the absence of STN8 is sufficient to abolish PCPP in osstn8 mutants and to produce all of the phenotypes observed in the double mutant of Arabidopsis, indicating the essential role of STN8-mediated PCPP in PSII repair.

Original languageEnglish
Pages (from-to)675-686
Number of pages12
JournalPlant Journal
Volume76
Issue number4
DOIs
StatePublished - Nov 2013

Keywords

  • D1 protein degradation
  • high light illumination
  • photosystem II core protein phosphorylation
  • photosystem II repair
  • rice
  • STN8 kinase

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