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Saxena, A. S.

Publications and source records attributed to Saxena, A. S..

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Head-to-Head Comparison of Three Methods of Quantifying Competitive Fitness in C. elegans

Organismal fitness is relevant in many contexts in biology. The most meaningful experimental measure of fitness is competitive fitness, when two or more entities (e.g., genotypes) are allowed to compete directly. In theory, competitive fitness is simple to measure: an experimental population is initiated with the different types in known proportions and allowed to evolve under experimental conditions to a predefined endpoint. In practice, there are several obstacles to obtaining robust estimates of competitive fitness in multicellular organisms, the most pervasive of which is simply the time it takes to count many individuals of different types from many replicate populations. Methods by which counting can be automated in high throughput are desirable, but for automated methods to be useful, the bias and technical variance associated with the method must be (a) known, and (b) sufficiently small relative to other sources of bias and variance to make the effort worthwhile.\n\nThe nematode Caenorhabditis elegans is an important model organism, and the fitness effects of genotype and environmental conditions are often of interest. We report a comparison of three experimental methods of quantifying competitive fitness, in which wild-type strains are competed against GFP-marked competitors under standard laboratory conditions. Population samples were split into three replicates and counted (1) \"by eye\" from a saved image, (2) from the same image using CellProfiler image analysis software, and (3) with a large particle flow cytometer (a \"worm sorter\"). From 720 replicate samples, neither the frequency of wild-type worms nor the among-sample variance differed significantly between the three methods. CellProfiler and the worm sorter provide at least a tenfold increase in sample handling speed with little (if any) bias or increase in variance.

evolutionary biology

Tempo, mode, and fitness effects of mutation in Caenorhabditis elegans over 400 generations of minimal selection

The mutational process varies at many levels, from within genomes to among taxa. Many mechanisms have been linked to variation in mutation, but understanding of the evolution of the mutational process is rudimentary. Physiological condition is often implicated as a source of variation in microbial mutation rate and may contribute to mutation rate variation in multicellular organisms.\n\nDeleterious mutations are a ubiquitous source of variation in condition. We test the hypothesis that the mutational process depends on the underlying mutation load in two groups of Caenorhabditis elegans mutation accumulation (MA) lines that differ in their starting mutation loads. \"First-Order MA\" (O1MA) lines maintained under minimal selection for [~]250 generations were divided into high-fitness and low-fitness groups and sets of \"second-order MA\" (O2MA) lines derived from each O1MA line were maintained for [~]150 additional generations. Genomes of 48 O2MA lines and their progenitors were sequenced. There is significant variation among O2MA lines in base-substitution rate ({micro}bs), but no effect of initial fitness, whereas the indel rate is greater in high-fitness O2MA lines. Overall, {micro}bs is positively correlated with recombination and proximity to short tandem repeats and negatively correlated with 10 bp and 1 Kb GC content. However, probability of mutation is well-predicted by the three-nucleotide motif. [~]90% of the variance in standing nucleotide variation is explained by mutability. Total mutation rate increased in the O2MA lines, as predicted by the \"drift barrier\" model of mutation rate evolution. These data, combined with experimental estimates of fitness, suggest that epistasis is synergistic.

evolutionary biology