S. Pursiheimo et al., Coregulation of light-harvesting complex II phosphorylation and lhcb mRNA accumulation in winter rye, PLANT J, 26(3), 2001, pp. 317-327
Winter rye plants grown under contrasting environmental conditions or just
transiently shifted to varying light and temperature conditions, were studi
ed to elucidate the chloroplast signal involved in regulation of photosynth
esis genes in the nucleus. Photosystem II excitation pressure, reflecting t
he plastoquinone redox state, and the phosphorylation level of thylakoid li
ght-harvesting proteins (LHCII and CP29) were monitored together with chang
es occurring in the accumulation of Ihcb, rbcS and psbA mRNAs. Short-term s
hifts of plants to changed conditions, from 1 h to 2 d, were postulated to
reveal signals crucial for the initiation of the acclimation process. Compa
rison of these results with those obtained from plants acclimated during se
veral weeks' growth at contrasting temperature and in different light regim
es, allow us to make the following conclusions: (1) LHCII protein phosphoyl
ation is a sensitive tool to monitor redox changes in chloroplasts; (2) LHC
II protein phosphorylation and Ihcb mRNA accumulation occur under similar c
onditions and are possibly coregulated via an activation state of the same
kinase (the LHCII kinase); (3) Maximal accumulation of Ihcb mRNA during the
diurnal light phase seems to require an active LHCII kinase whereas inacti
vation of the kinase is accompanied by dampening of the circadian oscillati
on in the amount of Ihcb mRNA; (4) Excitation pressure of photosystem II (r
eduction state of the plastoquinone pool) is not directly involved in the r
egulation of Ihcb mRNA accumulation. Instead (5) the redox status of the el
ectron accepters of photosystem I in the stromal compartment seems to be hi
ghly regulated and crucial for the regulation of Ihcb gene expression in th
e nucleus.