We analyze the effect of the plastoquinone redox state on the regulation of the light-harvesting antenna size at transcriptional and post-transcriptional levels. This was approached by studying transcription and accumulation of light-harvesting complexes in wild type versus the barley mutant viridis zb63, which is depleted in photosystem I and where plastoquinone is constitutively reduced. We show that the mRNA level of genes encoding antenna proteins is almost unaffected in the mutant; this stability of messenger level is not a peculiarity of antenna-encoding genes, but it extends to all photosynthesis-related genes. In contrast, analysis of protein accumulation by two-dimensional PAGE shows that the mutant undergoes strong reduction of its antenna size, with individual gene products having different levels of accumulation. We conclude that the plastoquinone redox state plays an important role in the long term regulation of chloroplast protein expression. However, its modulation is active at the post-transcriptional rather than transcriptional level.Sunlight is the only energy source for plants: light is absorbed by chlorophylls and carotenoids bound to the pigment-protein complexes composing photosystems I and II (PSI and -II), 2 and it is converted into chemical energy. Both photosystems are composed by two distinct moieties: (i) a core complex, responsible for charge separation and for the first steps of the electron transport, and (ii) an antenna system that increases light-harvesting capacity. In photosynthetic eukaryotes, the antenna system is composed by the members of a multigenic family called Lhc (light-harvesting complexes) (1). To avoid the over-accumulation of excitation energy in photosystems, light-absorption capacity needs to be related to the electron transport rate. To this purpose, the number of antenna proteins associated to photosystems is regulated according to the environmental conditions (2). More recently it was shown that the regulation of antenna size is restricted to PSII, whereas PSI-LHCI stoichiometry remains constant (3). Besides antenna size regulation, other mechanisms, like the state transition, the adjustment of PSI/PSII ratio, and regulation of carotenoid biosynthesis, are also involved in the plant's long term acclimation to different conditions (4). The limiting step of electron transport chain from PSII to PSI is the oxidation of plastoquinol (PQ) by cytochrome b 6 f (5); the PQ pool redox state depends on PSII excitation pressure, on the donor side, on the PSI capacity as acceptor, and on the rate of PQ reduction by cyclic electron transport (6). Thus, the ratio between reduced and oxidized plastoquinone is considered a good indicator of the balance between light absorption and electron transport rate: PQ over-reduction, in fact, suggests that electron transport is unable to use all the energy absorbed by PSII, where accumulation of excited states easily leads to the formation of harmful reactive oxygen species (ROS) (7). Thus, it is not surprising that the PQ pool redox ...