The organization and control of polarized growth through the cell cycle of Schizosaccharomyces pombe, a single-celled eukaryote, have been studied extensively. We have investigated the changes in these processes when S. pombe differentiates to form multicellular invasive mycelia and have found striking alterations to the behavior of some of the key regulatory proteins. Cells at the tips of invading filaments are considerably more elongated than cells growing singly and grow at one pole only. The filament tip follows a strict direction of growth through multiple cell cycles. A group of proteins involved in the growth process and actin regulation, comprising Spo20, Bgs4, activated Cdc42, and Crn1, are all concentrated at the growing tip, unlike their distribution at both ends of single cells. In contrast, several proteins implicated in microtubule-dependent organization of growth, including Tea1, Tea4, Mod5, and Pom1, all show the opposite effect and are relatively depleted at the growing end and enriched at the nongrowing end, although Tea1 appears to continue to be delivered to both ends. A third group acting at different stages of the cell cycle, including Bud6, Rga4, and Mid1, localize similarly in filaments and single cells, while Nif1 shows a reciprocal localization to Pom1.The fission yeast Schizosaccharomyces pombe has been used extensively as a model to study the control and morphology of a eukaryotic cell cycle. As a simple rod-shaped cell, it grows by elongation and divides by medial fission. Growth at each end is strictly controlled during the cycle. After division, growth occurs only at the "old" end, but after S phase is completed, growth commences at the "new" end, a stage known as newend take-off (NETO). The molecular basis of this ordered and polarized growth, which involves the actin cytoskeleton at the cell tips and microtubules to impose longer-range order, has been studied intensively (12). The Tea1 protein plays a key role in this process. It is delivered to cell tips on the plus ends of growing microtubules and accumulates at both tips even when only one end is growing. It and associated proteins in turn regulate, among other factors, the For3 formin and the GTPbinding protein Cdc42, both of which are involved in regulating actin-dependent tip growth. The site of cell division is marked by the anilin-related Mid1, while the Pom1 kinase interacts with all of these, apparently forming a concentration gradient that controls the timing of cell division (13,20). These and other proteins form a group of reinforcing functional modules which combine to produce the characteristically uniform pattern of growth of the S. pombe cell.