The unicellular green alga Acetabularia acetabulum has proven itself to be a superior model for studies of morphogenesis because of its large size and distinctive polar morphology. The giant cell forms an elongated tube (a stalk of up to 60 mm in length), which at its apical pole makes whorls of hairs, followed by one whorl of gametophores in the shape of a cap. At its basal pole, the cell extends into a rhizoid wherein the single nucleus is positioned. In this study, we have determined the level of specific messenger RNAs in the apical, middle, and basal regions using reverse transcriptase-PCR methodology. Four mRNA classes were distinguished: those that were uniformly distributed (small subunit of Rubisco, actin-1, ADPglucose, centrin, and ␣-and -tubulin), those that expressed apical/basal (calmodulin-4) or basal/apical gradients (calmodulin-2 and a Ran-G protein), and those with development-specific patterns of distribution (mitogen-activated protein kinase, actin-2, and UDP-glucose-epimerase). Restoration of the apical/basal calmodulin-4 mRNA gradient after amputation of the apical region of the cell requires the nucleus and was abolished by cytochalasin D. Accumulation of actin-1 mRNA in the vicinity of the wound set by the amputation needs, likewise, the presence of the nucleus and was also inhibited by cytochalasin. This suggests that actin microfilaments of the cytoskeleton are involved in directed transport and/or anchoring of these mRNAs.In the early 1930s, Haemmerling (1931, 1932, 1934a) introduced the unicellular green alga Acetabularia acetabulum (formerly known as Acetabularia mediterranea) as a research object into cell biology primarily because of its large size and distinct polar morphology. The life cycle of A. acetabulum begins with the fusion of two isogametes to form a zygote, which, after attachment to a solid substratum, grows into a long, tube-shaped stalk. The stalk elongates at the tip, periodically forming lateral whorls of branched hairs. Morphogenesis at the apical pole is completed with formation of a whorl of gametophores known as the cap. In contrast, the basal pole ends in a short, convoluted rhizoid resembling the fingers of a gnarled hand wherein the nucleus is located during all vegetative stages of the cell cycle. Thus, both cellular poles of A. acetabulum execute very different morphogenetic programs (for details, see Berger and Kaever, 1992;Mandoli, 1998).Grafting experiments led Haemmerling to the conclusion that "morphogenetic substances" are released from the nucleus into the cytoplasm where they elicit cellular morphogenesis. He considered them to be "gene products of the nucleus," distinguishing between cap-, whorls of hair-, stalk-, and rhizoidforming substances (Haemmerling, 1934b). A major feature of Haemmerling's morphogenetic substances was their extreme stability, because enucleated cells could perform stalk-, hair-, and cap-formation for several weeks after removal of the nucleus (Haemmerling, 1932). When these concepts were formulated, neither the chemical ...