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Science 6 December 2002: Vol. 298. no. 5600, pp. 1942 - 1946 DOI: 10.1126/science.1072163
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Review
Generating and Exploiting Polarity in Bacteria
Lucy Shapiro,1*
Harley H. McAdams,1
Richard Losick2
Bacteria are often highly polarized, exhibiting specialized
structures at or near the ends of the cell. Among such structures are
actin-organizing centers, which mediate the movement of certain pathogenic bacteria within the cytoplasm of an animal host cell; organized arrays of membrane receptors, which govern chemosensory behavior in swimming bacteria; and asymmetrically positioned septa, which generate specialized progeny in differentiating bacteria. This
polarization is orchestrated by complex and dynamic changes in the
subcellular localization of signal transduction and cytoskeleton proteins as well as of specific regions of the chromosome. Recent work
has provided information on how dynamic subcellular localization occurs
and how it is exploited by the bacterial cell.
The main task of a bacterial cell is
to survive and duplicate itself. The bacterium must replicate its
genetic material and divide at the correct site in the cell and at the
correct time in the cell cycle with high precision. Each kind of
bacterium also executes its own strategy to find nutrients in its
habitat and to cope with conditions of stress from its environment.
This involves moving toward food, adapting to environmental extremes, and, in many cases, entering and exploiting a eukaryotic host. These
activities often involve processes that take place at or near the poles
of the cell. Here we explore some of the schemes bacteria use to
orchestrate dynamic changes at their poles and how these polar events
execute cellular functions.
In spite of their small size, bacteria have a remarkably complex
internal organization and external architecture. Bacterial cells are
inherently asymmetric, some more obviously so than others. The most
easily recognized asymmetries involve surface structures, e.g.,
flagella, pili, and stalks that are preferentially assembled at one
pole by many bacteria. "New" poles generated at the cell division
plane differ from old poles from the previous round of cell division.
Even in Escherichia coli, which is generally thought to be
symmetrical, old poles are more static than new poles with respect to
cell wall assembly (1), and they differ in the deposition of
phospholipid domains (2). There are many instances of
differential polar functions; among these is the preferential use of
old poles when attaching to host cells as in the interaction of
Bradyrhizobium with plant root hairs (3) or the
polar pili-mediated attachment of the Pseudomonas aeruginosa
pathogen to tracheal epithelia (4). An unusual polar
organelle that mediates directed motility on solid surfaces is found in
the nonpathogenic bacterium Myxococcus xanthus. The gliding
motility of this bacterium is propelled by a nozzle-like structure that
squirts a polysaccharide-containing slime from the pole of the cell
(5). Interestingly, M. xanthus, which has nozzles
at both poles, can reverse direction by closing one nozzle and opening
the other in response to end-to-end interactions between cells.
1 Department of Developmental Biology, Stanford
University School of Medicine, B300 Beckman Center, Stanford, CA 94305, USA.
2 Department of Molecular and Cellular Biology,
Harvard University, Cambridge, MA 02138, USA.
*
To whom correspondence should be addressed. E-mail:
shapiro{at}cmgm.stanford.edu
Read the Full Text
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