Physcomitrella PIN localization usually formed a conspicuous banding pattern traversing the adaxial-abaxial leaf axis, where two cells contact one another ( Figures 3 and S3). Where leaves were thickened around the midvein, we also detected signal on the cell faces that were in contact with other cells, but the outermost cell Panobinostat in vitro faces were usually free from signal. Although we cannot rule out the possibility that each neighboring cell contributes to the high signal intensity at cell junctions, in our view, the localization is polarized.

As auxin-treated gametophores and pinA pinB mutants have around half the number of cells in the mediolateral leaf axis than normal and the mediolateral leaf axis is elaborated by asymmetric cell divisions [ 61], a polar localization pattern perpendicular to the mediolateral axis is consistent

with a role for PINA and PINB in promoting asymmetric cell division. These results suggest a role for canonical Physcomitrella PINs in intercellular polar auxin transport in leaf development. Recent work was unable to detect polar auxin transport in gametophytic moss shoots, and no effect of treatment with transport inhibitors was observed, leading to the conclusion that auxin transport does not contribute Dabrafenib mw to gametophore development [32 and 33]. We were also unable to detect long-range polar auxin transport using radio-labeled IAA (data not shown). The discrepancy between the results that we obtained with NPA and previously published results arises from a difference in experimental approach. Whereas previous experiments immersed fully grown shoots in 50 μM NPA [32 and 33], we grew colonies on NPA, exposing shoots to transport inhibition from the earliest developmental stages, and cotreatment

with low auxin concentrations was needed to see strong developmental effects (Figure 2). GPX6 We found that treatment of WT gametophores with NPA disrupted extension of proximodistal and mediolateral axes of leaf development and disrupted meristem function. The effects observed were similar to treatments with high concentrations of auxin or treatments of pinA mutants with low concentrations of auxin. Again, these results support a role for PIN-mediated auxin transport in the asymmetric cell divisions that drive leaf development and meristem function [ 61]. Consistent with PIN localization patterns, we hypothesize that auxin transport in moss gametophores occurs in a localized manner, to remove auxin from the leaves and meristem without detectable long-distance flux [ 62]. It is also possible that Physcomitrella PINs distribute auxin principally in the epidermis and, therefore, that the overall levels of transport involved are low.