Fitness effects of altering gene expression noise in <i>Saccharomyces cerevisiae</i>

Gene expression noise is an evolvable property of biological systems that describes differences in expression among genetically identical cells in the same environment. Prior work has shown that expression noise is heritable and can be shaped by selection, but the impact of variation in expression noise on organismal fitness has proven difficult to measure. Here, we quantify the fitness effects of altering expression noise for the TDH3 gene in Saccharomyces cerevisiae. We show that increases in expression noise can be deleterious or beneficial depending on the difference between the average expression level of a genotype and the expression level maximizing fitness. We also show that a simple model relating single-cell expression levels to population growth produces patterns consistent with our empirical data. We use this model to explore a broad range of average expression levels and expression noise, providing additional insight into the fitness effects of variation in expression noise

Empirical distributions of mutational effects define gene-specific neutral models of regulatory evolution

Poster presented at GSA PEQG 201

Classification of vocalizations of killer whales using dynamic time warping

A large number of killer whale sounds have recently been classified perceptually into Call Types. [A. Hodgins-Davis, thesis, Wellesley College (2004)]. The repetition rate of the pulsed component of five or more examples of each call type has been calculated using a modified form of the FFT based comb-filter method. A dissimilarity or distance matrix for these sounds was calculated using dynamic time warping to compare their melodic contours. These distances were transformed into a component space using multidimensional scaling and the resulting points were clustered with a kmeans algorithm. In grouping 57 sounds into 9 call types, a single discrepancy between the perceptual and the automated methods occurred. (c) 2006 Acoustical Society of America.</p

Candida albicans selection for human commensalism results in substantial within-host diversity without decreasing fitness for invasive disease.

Candida albicans is a frequent colonizer of human mucosal surfaces as well as an opportunistic pathogen. C. albicans is remarkably versatile in its ability to colonize diverse host sites with differences in oxygen and nutrient availability, pH, immune responses, and resident microbes, among other cues. It is unclear how the genetic background of a commensal colonizing population can influence the shift to pathogenicity. Therefore, we examined 910 commensal isolates from 35 healthy donors to identify host niche-specific adaptations. We demonstrate that healthy people are reservoirs for genotypically and phenotypically diverse C. albicans strains. Using limited diversity exploitation, we identified a single nucleotide change in the uncharacterized ZMS1 transcription factor that was sufficient to drive hyper invasion into agar. We found that SC5314 was significantly different from the majority of both commensal and bloodstream isolates in its ability to induce host cell death. However, our commensal strains retained the capacity to cause disease in the Galleria model of systemic infection, including outcompeting the SC5314 reference strain during systemic competition assays. This study provides a global view of commensal strain variation and within-host strain diversity of C. albicans and suggests that selection for commensalism in humans does not result in a fitness cost for invasive disease