We have determined the levels of photosystem 11 activity and polypeptide abundance in whole leaves and isolated bundle sheath and mesophyll cells of C4, "C4-like," and C3 species of the genus Flaverla (Asteraceae). On a chlorophyll basis, the whole leaf levels of the DI, D2, and 34-kilodalton photosystem 11 polypeptides were similar for each Flaveria species. Photosystem II activity varied twofold, but was not correlated with photosynthetic type (C3 or C4). The bundle sheath cell levels of photosystem 11 activity and associated polypeptides in C4-like and C4 Flaveria species were approximately one-half those observed in mesophyll cells but equivalent to those in bundle sheath cells of the C3 species, Flaveria cronquistll. Analyses of the steady-state levels of transcripts encoding photosystem 11 polypeptides indicated that there were no differences in transcript abundance between mesophyll and bundle sheath cells of the C4 Flaveria species. This pattem was in contrast to the three-to tenfold higher levels of transcripts encoding photosystem 11 polypeptides in mesophyll versus bundle sheath cells of maize. It is apparent that the higher mesophyll cell to bundle sheath ratio of photosystem 11 polypeptides in C4-and C4-like species of Flaveria is the result of higher levels of photosystem 11 expression in mesophyll cells rather than lower levels of expression in bundle sheath cells.generation ofelevated CO2 concentrations in the BSC, leading to a reduction in photorespiratory activities (6).The tissue-specific expression of C3 and C4 cycle enzymes is determined by developmentally regulated processes as well as by environmental (light) signals and may be regulated at the transcriptional and/or posttranscriptional level (4,10,12,15,20,23,25,28). In addition, the expression of some enzymes, e.g. Rubisco, requires the coordinate synthesis and assembly of subunits encoded by two separate genomes (chloroplast and nuclear) (4,15,25,26,28).To date, the molecular characterization of the expression of multi-subunit enzyme complexes in C4 plants has largely focused on this two subunit enzyme complex, Rubisco (4,25,27). Another multi-subunit enzyme complex that is expressed in a tissue-specific manner in NADP-ME type C4 plants is 11,26,28). The PSII complex is composed of more than 10 polypeptides which are both nuclear and chloroplast encoded and is expressed predominantly in the MC ofNADP-ME enzyme type C4 plants (17,23,26). Studies on the localization and expression of the PSII activity and polypeptides in C4 plants have, however, been limited to monocots such as maize and sorghum. In this study we have characterized the pattern of expression of PSII activity and polypeptides in C3, "C4-like," and C4 species of Flaveria (dicot).A characteristic feature of C4 plants is the differentiation of the photosynthetic tissues ofleaves into two distinct cell types, MC3 and BSC. These cells contain different complements of enzymes active in photosynthetic CO2 fixation (5). For example, PEPCase, the C4 cycle enzyme that catalyz...