Michael S Barker

Michael S Barker

Associate Professor, Ecology and Evolutionary Biology
Associate Department Head, Ecology and Evolutionary Biology
Associate Professor, BIO5 Institute
Member of the General Faculty
Member of the Graduate Faculty
Primary Department
Contact
(520) 621-2213

Research Interest

Michael Barker is an evolutionary biologist studying the origins of biological diversity, particularly how abrupt genomic changes such as polyploidy, chromosomal change, and hybridization have contributed to the evolution of plant diversity. Biologists have long been fascinated by these processes because they create unique opportunities for the evolution of ecological and phenotypic novelty with the potential for relatively rapid speciation. Although assessing the importance of these abrupt changes has historically been a difficult task, advances in genomics and bioinformatics have created new opportunities for addressing these longstanding questions. By integrating new computational and evolutionary genomic tools with traditional approaches such as molecular evolution, phylogenetics, mathematical modeling, and experimental work Barker's lab currently studies 1.) the contributions of recent and ancient polyploidy to eukaryotic diversity; 2.) the evolution of chromosome number and genome organization; and 3.) the impact of hybridization on speciation and novelty.

Publications

Hodgins, K. A., Lai, Z., Oliveira, L. O., Still, D. W., Scascitelli, M., Barker, M. S., Kane, N. C., Dempewolf, H., Kozik, A., Kesseli, R. V., Burke, J. M., Michelmore, R. W., & Rieseberg, L. H. (2014). Genomics of compositae crops: Reference transcriptome assemblies and evidence of hybridization with wild relatives. Molecular Ecology Resources, 14(1), 166-177.

Abstract:

Although the Compositae harbours only two major food crops, sunflower and lettuce, many other species in this family are utilized by humans and have experienced various levels of domestication. Here, we have used next-generation sequencing technology to develop 15 reference transcriptome assemblies for Compositae crops or their wild relatives. These data allow us to gain insight into the evolutionary and genomic consequences of plant domestication. Specifically, we performed Illumina sequencing of Cichorium endivia, Cichorium intybus, Echinacea angustifolia, Iva annua, Helianthus tuberosus, Dahlia hybrida, Leontodon taraxacoides and Glebionis segetum, as well 454 sequencing of Guizotia scabra, Stevia rebaudiana, Parthenium argentatum and Smallanthus sonchifolius. Illumina reads were assembled using Trinity, and 454 reads were assembled using MIRA and CAP3. We evaluated the coverage of the transcriptomes using BLASTX analysis of a set of ultra-conserved orthologs (UCOs) and recovered most of these genes (88-98%). We found a correlation between contig length and read length for the 454 assemblies, and greater contig lengths for the 454 compared with the Illumina assemblies. This suggests that longer reads can aid in the assembly of more complete transcripts. Finally, we compared the divergence of orthologs at synonymous sites (Ks) between Compositae crops and their wild relatives and found greater divergence when the progenitors were self-incompatible. We also found greater divergence between pairs of taxa that had some evidence of postzygotic isolation. For several more distantly related congeners, such as chicory and endive, we identified a signature of introgression in the distribution of Ks values. © 2013 John Wiley & Sons Ltd.

Barker, M. S., & Hickey, R. J. (2006). A taxonomic revision of Caribbean Adiantopsis (Pteridaceae). Annals of the Missouri Botanical Garden, 93(3), 371-401.

Abstract:

Adiantopsis Fée (Pteridaceae) is a relatively unstudied tropical cheilanthoid fern genus. In the present work, we evaluated the taxonomy and relationships among Caribbean Adiantopsis by examining 136 characters from approximately 500 herbarium specimens. This study identified nine Caribbean Adiantopsis species, three of which are newly described (A. parvisegmenta, A. pentagona, and A. vincentii). Additionally, an intriguing pattern of morphological and reticulate evolution was revealed by the analyses. Adiantopsis consists of three different laminar morphologies; palmate, pedate, and pinnate. The two pedate taxa are hypothesized to be fertile allotetraploid derivatives of the palmate A. radiata (L.) Fée and two different pinnate taxa. In this regard they parallel the origin of the South American A. Xaustralopedata Hickey, M. S. Barker & Ponce. Based on our analyses, it appears that pedate laminar morphologies in Adiantopsis independently originated multiple times via hybridization. This study provides testable hypotheses of morphological and reticulate evolution in the genus and presents a novel view of Caribbean Adiantopsis.

Barker, M. S., Demuth, J. P., & Wade, M. J. (2005). Maternal expression relaxes constraint on innovation of the anterior determinant, bicoid.. PLoS genetics, 1(5), e57.

PMID: 16299585;PMCID: PMC1283158;Abstract:

The origin of evolutionary novelty is believed to involve both positive selection and relaxed developmental constraint. In flies, the redesign of anterior patterning during embryogenesis is a major developmental innovation and the rapidly evolving Hox gene, bicoid (bcd), plays a critical role. We report evidence for relaxation of selective constraint acting on bicoid as a result of its maternal pattern of gene expression. Evolutionary theory predicts 2-fold greater sequence diversity for maternal effect genes than for zygotically expressed genes, because natural selection is only half as effective acting on autosomal genes expressed in one sex as it is on genes expressed in both sexes. We sample an individual from ten populations of Drosophila melanogaster and nine populations of D. simulans for polymorphism in the tandem gene duplicates bcd, which is maternally expressed, and zerknüllt (zen), which is zygotically expressed. In both species, we find the ratio of bcd to zen nucleotide diversity to be two or more in the coding regions but one in the noncoding regions, providing the first quantitative support for the theoretical prediction of relaxed selective constraint on maternal-effect genes resulting from sex-limited expression. Our results suggest that the accelerated rate of evolution observed for bcd is owing, at least partly, to variation generated by relaxed selective constraint.

Barker, M. S., Dlugosch, K. M., Dinh, L., Challa, R. S., Kane, N. C., King, M. G., & Rieseberg, L. H. (2010). Evopipes.net: Bioinformatic tools for ecological and evolutionary genomics. Evolutionary Bioinformatics, 2010(6), 143-149.

PMID: 21079755;PMCID: PMC2978936;Abstract:

Recent increases in the production of genomic data are yielding new opportunities and challenges for biologists. Among the chief problems posed by next-generation sequencing are assembly and analyses of these large data sets. Here we present an online server, http://EvoPipes.net, that provides access to a wide range of tools for bioinformatic analyses of genomic data oriented for ecological and evolutionary biologists. The EvoPipes.net server includes a basic tool kit for analyses of genomic data including a next-generation sequence cleaning pipeline (SnoWhite), scaffolded assembly software (SCARF), a reciprocal best-blast hit ortholog pipeline (RBH Orthologs), a pipeline for reference protein-based translation and identification of reading frame in transcriptome and genomic DNA (TransPipe), a pipeline to identify gene families and summarize the history of gene duplications (DupPipe), and a tool for developing SSRs or microsatellites from a transcriptome or genomic coding sequence collection (findSSR). EvoPipes.net also provides links to other software developed for evolutionary and ecological genomics, including chromEvol and NU-IN, as well as a forum for discussions of issues relating to genomic analyses and interpretation of results. Overall, these applications provide a basic bioinformatic tool kit that will enable ecologists and evolutionary biologists with relatively little experience and computational resources to take advantage of the opportunities provided by next-generation sequencing in their systems. © the author(s), publisher and licensee Libertas Academica Ltd.

Marques, I., Montgomery, S. A., Barker, M. S., Macfarlane, T. D., Conran, J. G., Catal{\'a}n, P., Rieseberg, L. H., Rudall, P. J., & Graham, S. W. (2015). Transcriptome-derived evidence supports recent polyploidization and a major phylogeographic division in Trithuria submersa (Hydatellaceae, Nymphaeales). New Phytologist.