Volume 22, Issue 16, Pages R620-R622 (August 2012) Candida albicans  Judith Berman  Current Biology  Volume 22, Issue 16, Pages R620-R622 (August 2012) DOI: 10.1016/j.cub.2012.05.043 Copyright © 2012 Elsevier Ltd Terms and Conditions

Figure 1 Fluorescent protein fusions in Candida albicans. Useful fluorescent markers for tracking subcellular structures in C. albicans include: DAPI (DNA); Nop1-GFP (green fluorescent protein, localizing to the nucleolus); Hhf1-GFP (chromatin); Tub2-GFP (microtubules, green); and Tub4-mCherry fluorescent protein (spindle pole bodies, red). Micrographs courtesy of Shelly Applen and Benjamin Harrison. Current Biology 2012 22, R620-R622DOI: (10.1016/j.cub.2012.05.043) Copyright © 2012 Elsevier Ltd Terms and Conditions

Figure 2 Phenotypic switching in Candida albicans. Growth of C. albicans cells on phloxine plates detects colonies of cells that are either white (white colonies) or opaque (pink colonies) (left panel). A subset of cells in a mostly white colony switched to the opaque state, forming a sector in the colony (right panel). Photos courtesy of Meleah Hickman. Current Biology 2012 22, R620-R622DOI: (10.1016/j.cub.2012.05.043) Copyright © 2012 Elsevier Ltd Terms and Conditions