Boris Igic

Associate Professor

Education:  PhD, University of California, San Diego

Website: Dr. Igic's Lab

About Dr. Igic's Research
[Please go to the lab webpage, linked above, for a complete publication list and other detailed information.]

My lab seeks to advance our understanding of mating system evolution, and more broadly the patterns and causes of trait changes and their effects on diversification.

Mating systems have wide-ranging effects, including the their strong causal association with the magnitude and distribution of genetic diversity. Our work has long aimed to uncover both the causes and consequences of mating system transitions and the observed variation in mating systems within and between species. We are presently engaged in an effort to generate massively parallel  sequence data for the inference of population genetic patterns and phylogenetic relationships in the nightshade plant family (Solanaceae). We continue to work on detecting and fixing the multitude of problems with macroevolutionary inference of trait evolution (Igic et al. 2006, Goldberg and Igic 2008, 2012).. One of the goals of this line of research is to properly order breeding and mating system transitions and ask how contrasting mating systems influence evolutionary fate of lineages.

We are also interested in the link between genotype, phenotype, and environment. Until recently, we pursued this interest principally in the context of self-incompatibility systems, where the fitness consequences of new phenotypic variants are well understood. Self-incompatibility (SI) is defined as the ability of plants to recognize and reject their own pollen. It commonly involves linked pollen- and style-expressed genes, which must co-evolve to maintain the ability to recognize each other. Genes associated with self-recognition systems such as SI in plants, mating type loci in fungi, the sex determination locus in hymenopterans, and the MHC in jawed vertebrates experience selection for rare alleles, and thus harbor extreme allelic polymorphism. This polymorphism is typically manifested as a spectacular number of alleles maintained in natural populations (up to 200; Lawrence 2000), and high molecular divergence among alleles (Ioerger et al. 1990), implying long times to coalescence of allelic polymorphism. Because of its unique characteristics, the study of SI can provide information concerning historical population genetic changes (e.g. bottlenecks; Richman et al. 1996, Igic et al. 2004), the order of mating system transitions (Igic et al. 2004, 2006, 2008; Goldberg et al. 2010), and provide insights into the link between nucleotide transitions, traits, and ecological setting.

In addition, the lab is entering a number of exciting collaborations aimed at improving the methods for reconstruction of ancestral states and detection of differential diversification rates in a variety of traits not confined to plant lineages, finding co-evolved regions/residues of interacting molecules under positive selection (in the absence of experimental evidence), and identifying genomic regions and genes responsible for reproductive isolation and ecological divergence between species.

Literature Cited

  • Igic, B., L. Bohs, and J.R. Kohn. 2004. Historical inferences from the self-incompatibility locus. New Phytologist 161:97-105.

  • Igic, B., L. Bohs, and J.R. Kohn. 2006. Ancient polymorphism reveals unidirectional breeding system shifts. Proceedings of the National Academy of Sciences 103:1359-1363.

  • Igic, B. and J.R. Kohn. 2006. Bias in the studies of outcrossing rate distributions. Evolution 60:1098-1103.

  • Ioerger, T. R., A. G. Clark, and T.-h. Kao. 1990. Polymorphism at the self-incompatibility locus in Solanaceae predates speciation. Proceedings of the National Academy of Sciences 87:9732-9735.

  • Lawrence, M.J. 2000. Population genetics of homomorphic self-incompatibility polymorphisms in flowering plants. Annals of Botany 85:221-226.

  • Richman, A. D., M. K. Uyenoyama, and J. R. Kohn. 1996. Allelic diversity and gene genealogy at the self-incompatibility locus in the Solanaceae. Science 273:1212-1216.

  • Stebbins, G. L. 1957. Self fertilization and population variability in the higher plants. American Naturalist 91:337-354.

Representative Publications 
(Complete list of publications on Google Scholar)

  • Igic, B. and J. W. Busch. 2013. Is self-fertilization an evolutionary dead end? New Phytologist 198:386-397.
  • Goldberg, E. E. and B. Igic. 2012. Tempo and mode in plant breeding system evolution. Evolution 66:3701-3709.
  • Goldberg E.E., J.R. Kohn, R. Lande, K.A. Robertson, S.A. Smith, and B. Igic. 2010. Species selection maintains self-incompatibility. Science 330: 459-460.
  • Goldberg E.E. and B. Igic. 2008. On phylogenetic tests of irreversible evolution. Evolution 62: 2727-2741.
  • Igic B., R. Lande, and J.R. Kohn. 2008. Loss of self-incompatibility and its evolutionary consequences. International Journal of Plant Sciences 169: 93-104.
  • Igic B., W.A. Smith, K. Robertson, B.A. Schaal, and J.R. Kohn. 2007. The population genetics of the self-incompatibility polymorphism in wild tomatoes: I. S-RNase diversity in Solanum chilense (Dun.) Reiche (Solanaceae). Heredity 99: 553-561.
  • Igic B., L. Bohs, and J.R. Kohn. 2006. Ancient polymorphism reveals unidirectional breeding system transitions. Proceedings of the National Academy of Sciences 103: 1359-1363.
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Contact Information

Phone: 312-996-6072