Knockdown of the A rabidopsis thaliana chloroplast protein disulfide isomerase 6 results in reduced levels of photoinhibition and increased D 1 synthesis in high light

A chloroplast protein disulfide isomerase ( PDI ) was previously proposed to regulate translation of the unicellular green alga C hlamydomonas reinhardtii chloroplast psb A m RNA , encoding the D 1 protein, in response to light. Here we show that A t PDI 6, one of 13 A rabidopsis thaliana   PDI gene...

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Veröffentlicht in:The Plant journal : for cell and molecular biology 2014-06, Vol.78 (6), p.1003-1013
Hauptverfasser: Wittenberg, Gal, Levitan, Alexander, Klein, Tamir, Dangoor, Inbal, Keren, Nir, Danon, Avihai
Format: Artikel
Sprache:eng
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Zusammenfassung:A chloroplast protein disulfide isomerase ( PDI ) was previously proposed to regulate translation of the unicellular green alga C hlamydomonas reinhardtii chloroplast psb A m RNA , encoding the D 1 protein, in response to light. Here we show that A t PDI 6, one of 13 A rabidopsis thaliana   PDI genes, also plays a role in the chloroplast. We found that A t PDI 6 is targeted and localized to the chloroplast. Interestingly, A t PDI 6 knockdown plants displayed higher resistance to photoinhibition than wild‐type plants when exposed to a tenfold increase in light intensity. The A t PDI 6 knockdown plants also displayed a higher rate of D 1 synthesis under a similar light intensity. The increased resistance to photoinhibition may not be rationalized by changes in antenna or non‐photochemical quenching. Thus, the increased D 1 synthesis rate, which may result in a larger proportion of active D 1 under light stress, may led to the decrease in photoinhibition. These results suggest that, although the D 1 synthesis rates observed in wild‐type plants under high light intensities are elevated, repair can potentially occur faster. The findings implicate A t PDI 6 as an attenuator of D 1 synthesis, modulating photoinhibition in a light‐regulated manner.
ISSN:0960-7412
1365-313X
DOI:10.1111/tpj.12525