Thomas D. Cabot Associate Professor of Organismic and Evolutionary Biology
Office: Biolabs 1105, 16 Divinity Avenue
Lab Website: http://www.oeb.harvard.edu/faculty/bomblies/
The main interest of the lab is to understand the molecular mechanisms of evolutionary adaptation, but we see this broadly to include adaptation to both the internal environment (adaptation to changes in the genome) and the external environment (habitat adaptation). We work mostly with Arabidopsis arenosa, which we have been developing as a molecular model system. This lovely relative of A. thaliana is an obligate outcrosser, tetraploid through most of its range but with an extant diploid variant, and widely distributed in Europe. Populations vary considerably in a number of interesting potentially adapative traits as well as in ploidy.
(1) Adaptation to whole genome duplication. Arabidopsis arenosa is autotetraploid through most of its central European range (that is, it duplicated its entire genome via a within-species event that did not involve hybridization). The tetraploids, like their diploid progenitors, are obligately outcrossing and fully fertile. From artificially doubled diploids, we know that the diploid genome is not already competent to sustain stable meiosis in the polyploid state, yet the established polyploids show cytologically diploid-like behavior (this was from our collaborators James Higgins and Chris Franklin at the University of Birmingham in the UK). This suggests that the established tetraploid has adapted to its polyploid genome state. What processes were modified and what protein functions changed to condition this is a question we are seeking to answer using a combination of genomics, transcriptomics, molecular genetics and cytology. In two genome scans we identified a set of genes that were likely important in tetraploid evolution. With genetic follow-up, we have shown that allelic variation in at least one of these genes has a dramatic effect on chromosome segregation in the tetraploids. We are currently following this up to understand the mechanism underlying this. We are also analyzing the molecular evolution of meiosis-related genes in diploid and tetraploid A. arenosa and have found intriguing patterns that are prompting us to explore the evolution of meiosis genes in greater detail.
(2) Biogeography and Habitat adaptation. Arabidopsis arenosa autotetraploids have adapted to a wide range of habitats, ranging from the apparently ancestral shaded limestone outcrop habitat to silicaceous outcrops, serpentine, railways, acid bogs, beaches, and heavy metal contaminated mine tailings. We are interested in understanding the genetic basis of their invasion of human-associated flatland railway habitats from ancestral mountain rock-outcrop habitats. The invasion of the the drier, hotter railway habitat (which also gets sprayed nearly annually with herbicide) is associated with a switch from perennial winter-dependent episodic flowering to an annual, rapid-cycling, perpetually flowering winter-independent habit. We are using population genomic as well as genetic approaches to explore the genetic basis of this adaptation, and are very interested in whether this involves the same genes or distinct ones from related well-characterized A. thaliana. We already have evidence that early flowering arose at least twice and apparently through independent molecular mechanisms in A. arenosa. Currently we are mapping the causal genes.
(3) Evolutionary dynamics of interacting genes. One striking observation from our genome scans is that signatures of selection are often seen in genes whose protein products are known to interact. Are these genes adaptating to their genomic context? Do they co-evolve as "adaptive modules" or do they all contribute additively to phenotype? Do they all need to be in the correct allelic state? We are currently exploring these questions with a large population resequencing study and follow-up experiments to test functional modules of related genes. We are particularly focused on several groups of functionally-connected meiosis genes that show evidence of having undergone selective sweeps in tetraploids, as well as in some cases already in diploids.
Current group members:
Ben Hunter – Senior Research Associate. Flowering time in A. arenosa. Molecular genetics of hybrid necrosis and temperature responses in A. thaliana.
Kevin Wright - Postdoc / NIH NRSA fellow. Meiotic adaptation in A. arenosa.
Jeremy O'Connell - Postdoc. Meiotic adaptation in A. arenosa.
Brian Arnold – PhD student. Population genetics and genomics of A. arenosa.
Pierre Baduel – PhD student. Flowering time adaptation in A. arenosa.
Yherson Franchesco Molina Henao – PhD student (starting fall 2013).
Julie Vu – Undergraduate research assistant. Adaptation of meiosis in A. arenosa.
Dina Benayad – High school student. Working with Kevin Wright on the molecular evolution of meiosis genes.
Yant, L.*, Hollister, J. D.*, Wright, K. M., Arnold, B. J., Higgins, J. D., Franklin, F. C. H. and Bomblies, K. (2013) Meiotic adaptation to genome duplication in Arabidopsis arenosa. Current Biology. 23, pp. 2151-2156. * = contributed equally.
Arnold, B.*, Corbett-Detig, R. B.*, Hartl, D. and Bomblies, K. (2013) RADseq underestimates diversity and introduces genealogical biases due to nonrandom haplotype sampling. Molecular Ecology, Vol 22: 3179-3190. * = contributed equally.
Wright, K. M., and Bomblies, K. (2013) Evolutionary genetics: Inheritance of a complex pollination syndrome. Dispatch article. Current Biology. 23, pp. R525-R527.
Hunter, B.*, Wright, K*., and Bomblies, K. (2013) Short read sequencing in studies of natural variation and adaptation. Curr Op in Plant Biology, 16 (1) 85-91.* equal contribution.
Bomblies, K. (2013) Genes causing postzygotic hybrid incompatibility in plants: A window into co-evolution, in Polyploid and Hybrid Genomics (eds Z. J. Chen and J. A. Birchler), John Wiley & Sons, Inc., Oxford, UK.
Hollister, J., Arnold, B., Svedin, E., Xue, K., Dilkes, B. and Bomblies, K. (2012) Genetic adaptation associated with genome-doubling in autotetraploid Arabidopsis arenosa. PLoS Genetics, 8(12): e1003093.
Arnold, B., Bomblies, K. and Wakeley, J. (2012) Extending coalescent theory to autotetraploids. Genetics. Vol 192, pp. 195-204.
Hunter, B., Hollister, J. D. and Bomblies, K. (2012) Epigenetic inheritance: What news for evolution? Current Biology. Dispatch article. Vol 22, pp. R54-R56.
Hunter, B. and Bomblies, K. (2010) The genetics of speciation in the Arabidopsis genus. Invited review. In: The Arabidopsis Book. American Society of Plant Biologists. Ames, IA
Bomblies, K. (2010). Doomed lovers: mechanisms of isolation and incompatibility in plant speciation. Invited review. Annual review of Plant Biology 61, pp. 109-124.
Bomblies, K. (2010) Evolution: Redundancy as an opportunity for innovation. Dispatch article. Current Biology. 20, pp. R320-R322.
Bomblies, K. (2009). Too much of a good thing? Hybrid necrosis as a by-product of plant immune system diversification. Invited review. Botany 87, pp. 1013-1022.
General Audience Publications
Bomblies, K. Plant Immunity in a changing world. Essay contribution to “Future Science – 19 essays from the Cutting Edge” edited by Max Brockmann (2011).
Bomblies, K. The stunning diversity of plants. 10 Questions Interview. Seed magazine. February 22, 2010.