My research uses evolutionary
and population genetic theory as a framework for understanding
the evolutionary significance of mutation rates and mutational
phenomena.
Because the ultimate source of genetic
variation is mutation, the evolution of mutation rates is a subject
of basic interest in genetics. Considerable health implications
exist as well: Recent findings have linked high somatic mutation
rates with certain cancers, and high mutation rates have also
been linked to pathogenicity in E. coli and Salmonella.
Defective methyl-directed mismatch repair (hereafter, MMR) is
implicated as the underlying mechanistic basis for high mutation
rates in both of these cases. However, the basis for the evolutionary
success of MMR-defective alleles remains to be examined rigorously.
I am currently studying experimental populations of the bacterium
Escherichia coli in which strikingly elevated general mutation
rates have evolved. Genetic complementation analyses have shown
that these high mutation rates are caused by defects in the MMR
pathway. I am using classical and molecular genetic approaches
to manipulate and characterize the specific MMR defects responsible
for the evolution of mutation rates, and I am pursuing experimental
and theoretical population genetic studies to examine the causes
of mutation rate evolution.
The genomes of virtually all organisms
well studied at the molecular level harbor transposable elements
(TEs), which are genetic entities capable of replicating faster
than host DNA and inserting replicas into new genomic locations.
TEs have been the subject of considerable speculation and interest;
opinion is broadly divided over whether they are of functional
or adaptive value or are best regarded as parasitic (selfish)
entities. Surveys of TEs in natural Drosophila melanogaster
populations have supported the selfish DNA view: TEs are rare
at occupied genomic sites, as would be expected on a balance between
selective elimination and replicative transposition. Very little
is known, however, about the population biology of TEs in other
taxa. I have recently initiated a project to study the population
genetics of Ty elements in the wild yeast Saccharomyces paradoxus,
a close congener to the domesticated brewer's yeast S. cerevisiae.
The early stages of this project are providing novel information
on the structure of wild yeast populations, and this information
will be used as a baseline for future studies of the significance
of Ty elements.
Sniegowski P. 1998. Mismatch
repair: origin of species?. [Review] [16 refs] Current Biology8(2):R59-61.
Lenski R.E., Mongold J.A., Sniegowski
P.D., Travisano M., Vasi F. Gerrish P.J., Schmidt T.M.
1998. Evolution of competitive fitness in experimental populations
of E. coli: what makes one genotype a better competitor
than another?. [Review] [29 refs] Antonie van Leeuwenhoek73(1):35-47.
Naumov, G.I., Naumova, E.S., Sniegowski
P.D. 1997. Differentiation of European and Far East Asian populations
of Saccharomyces paradoxus by allozyme analysis. International
Journal of Systematic Bacteriology47(2):341-4.
Sniegowski, P.D., Gerrish,
P.J., Lenski, R.E., 1997. Evolution of high mutation rates
in experimental populations of E. coli [see comments]. Nature387(6634):703-5.
Sniegowski P. 1997. Evolution:
setting the mutation rate. Current Biology7(8):R487-8.
Sniegowski, P. D. 1995.
A test of the directed mutation hypothesis in Escherichia coli MCS2
using replica plating. Journal of Bacteriology177:1119-1120.
Sniegowski, P. D. and R. E.
Lenski. 1995. Mutation and adaptation: The directed mutation
controversy in evolutionary perspective. Annual Review of
Ecology and Systematics26:553-578.
Sniegowski, P. D. and
B. Charlesworth. 1994. Transposable element numbers in cosmopolitan
inversions from a natural population of Drosophila melanogaster.
Genetics137:815-827.
Charlesworth, B., Sniegowski, P.
and W. Stephan. 1994. The evolutionary dynamics of repetitive
DNA in eukaryotes. Nature371:215-220.