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Cover We now take for granted that the basic components and mechanisms
of all eukaryotic cells are conserved. However, only 20 years ago the
relationship between animals and simple eukaryotes such as yeast was
not so clear. One of the hallmarks of eukaryotes is a cytoskeleton,
made up of actin filaments and microtubules. By 1984 it was known that
yeast had genes for actin and tubulin, and that the yeast actin and
tubulin proteins behaved in vitro like their animal counterparts, but
little was known of the structure and function of the yeast
cytoskeleton. Kilmartin and Adams (J. Cell Biol. [1984].
98, 922-933) adapted fluorescence microscopy techniques to
fixed yeast cells, revealing actin and microtubule structures that were
quite simple in comparison to those in animal cells. Although simple,
the yeast cytoskeleton was seen to change in characteristic ways during
the well-defined cell cycle. The cover figure shows the stages of the
cell cycle in cells of Saccharomyces uvarum (a close
relative of the more common Saccharomyces cerevisiae)
labeled with rhodamine-phalloidin (top) and anti-tubulin antibody. The
numbers below indicate the percent of cells in a growing population
showing the particular morphology. Filamentous actin is seen as
cortical dots, generally associated with points of cell growth, and as
fibers. Microtubules are seen as a bright intranuclear mitotic spindle
that lengthens during the cycle and fainter cytoplasmic microtubules.
This distribution of microtubules had been observed earlier in the
pioneering electron microscopy experiments of Breck Byers and
colleagues (Byers and Goetsch [1975]. J. Bacteriol. 124, 511-523). Soon after this work, conditional mutations were identified
in the actin and tubulin genes (Shortle et al. [1984].
Proc Natl. Acad. Sci. USA. 81, 4889-4893; Thomas
et al. [1985]. Genetics 111, 715-734),
allowing a genetic analysis of the functions of the yeast cytoskeleton.
This combination of genetics with morphological analysis has been
particularly powerful, and the current challenge is to relate the
wealth of information from the yeast genome sequence and associated
genome-wide phenotypic assays with functional studies on the yeast
cytoskeleton. The cover figure is reprinted from The Journal of
Cell Biology, 1984, 111, p. 715-734 by copyright permission of
The Rockefeller University Press.
Tim Stearns