Drosophila melanogaster Singh Lab Drosophila melanogaster
Home - People - Publications - Research - Photos - Joining the Lab - Contact Us - Relevant Links
DNA helix
Research

The challenge in genomics no longer lies in the production of sequence data, but rather, in their interpretation. My research program focuses on one aspect of this interpretation: deciphering genome-level patterns of genetic change. These patterns, observed as divergence between species or polymorphisms within species, are generated by all stages of the molecular evolutionary process, from the mutational generation of novel variants to the population level processes that lead to their fixation. We use laboratory, bioinformatic, and comparative genomic tools to quantify the individual and joint contributions of different evolutionary forces to genome evolution, such that the underlying causes of molecular change can be inferred.

We are currently focusing on heterogeneity in recombination intensity and mutation rate.

Meiotic recombination is a potent process that significantly impacts myriad aspects of genome evolution. Rates of recombination are known to vary among species, populations, and even among individuals. Different regions of the genome show varying rates of crossing-over as well, over both large and small chromosomal spans. However, the scale of this heterogeneity in recombination intensity and its molecular and genetic basis remain poorly understood. Thus, several outstanding questions remain. At what scale does recombination intensity vary, and to what degree? What is the genetic basis for heterogeneity in recombination intensity? Are the factors mediating variation in recombination intensity within populations the same as those mediating between-population differences? How labile is recombination intensity on an evolutionary timescale? We are addressing these questions using Drosophila as a model system by leveraging a combination of classical genetics and next-generation sequencing.

Previous work in Drosophila has indicated heterogeneity in patterns of single nucleotide substitution both within and between species. However, this heterogeneity could have arisen from underlying variation in mutation rate, or variation in the population process through which mutations are fixed or lost from the population. To distinguish between these possibilities, we are quantifying intra- and interspecific mutation rate variation in Drosophila using a combination of population genetic, molecular evolutionary, and experimental techniques.