J. Spencer Johnston
Texas A&M University
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Featured researches published by J. Spencer Johnston.
Science | 2007
Vishvanath Nene; Jennifer R. Wortman; Daniel John Lawson; Brian J. Haas; Chinnappa D. Kodira; Zhijian Jake Tu; Brendan J. Loftus; Zhiyong Xi; Karyn Megy; Manfred Grabherr; Quinghu Ren; Evgeny M. Zdobnov; Neil F. Lobo; Kathryn S. Campbell; Susan E. Brown; Maria F. Bonaldo; Jingsong Zhu; Steven P. Sinkins; David G. Hogenkamp; Paolo Amedeo; Peter Arensburger; Peter W. Atkinson; Shelby Bidwell; Jim Biedler; Ewan Birney; Robert V. Bruggner; Javier Costas; Monique R. Coy; Jonathan Crabtree; Matt Crawford
We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at ∼1376 million base pairs is about 5 times the size of the genome of the malaria vector Anopheles gambiae. Nearly 50% of the Ae. aegypti genome consists of transposable elements. These contribute to a factor of ∼4 to 6 increase in average gene length and in sizes of intergenic regions relative to An. gambiae and Drosophila melanogaster. Nonetheless, chromosomal synteny is generally maintained among all three insects, although conservation of orthologous gene order is higher (by a factor of ∼2) between the mosquito species than between either of them and the fruit fly. An increase in genes encoding odorant binding, cytochrome P450, and cuticle domains relative to An. gambiae suggests that members of these protein families underpin some of the biological differences between the two mosquito species.
Proceedings of the National Academy of Sciences of the United States of America | 2010
Ewen F. Kirkness; Brian J. Haas; Weilin Sun; Henk R. Braig; M. Alejandra Perotti; John M. Clark; Si Hyeock Lee; Hugh M. Robertson; Ryan C. Kennedy; Eran Elhaik; Daniel Gerlach; Evgenia V. Kriventseva; Christine G. Elsik; Dan Graur; Catherine A. Hill; Jan A. Veenstra; Brian Walenz; Jose M. C. Tubio; José M. C. Ribeiro; Julio Rozas; J. Spencer Johnston; Justin T. Reese; Aleksandar Popadić; Marta Tojo; Didier Raoult; David L. Reed; Yoshinori Tomoyasu; Emily Kraus; Omprakash Mittapalli; Venu M. Margam
As an obligatory parasite of humans, the body louse (Pediculus humanus humanus) is an important vector for human diseases, including epidemic typhus, relapsing fever, and trench fever. Here, we present genome sequences of the body louse and its primary bacterial endosymbiont Candidatus Riesia pediculicola. The body louse has the smallest known insect genome, spanning 108 Mb. Despite its status as an obligate parasite, it retains a remarkably complete basal insect repertoire of 10,773 protein-coding genes and 57 microRNAs. Representing hemimetabolous insects, the genome of the body louse thus provides a reference for studies of holometabolous insects. Compared with other insect genomes, the body louse genome contains significantly fewer genes associated with environmental sensing and response, including odorant and gustatory receptors and detoxifying enzymes. The unique architecture of the 18 minicircular mitochondrial chromosomes of the body louse may be linked to the loss of the gene encoding the mitochondrial single-stranded DNA binding protein. The genome of the obligatory louse endosymbiont Candidatus Riesia pediculicola encodes less than 600 genes on a short, linear chromosome and a circular plasmid. The plasmid harbors a unique arrangement of genes required for the synthesis of pantothenate, an essential vitamin deficient in the louse diet. The human body louse, its primary endosymbiont, and the bacterial pathogens that it vectors all possess genomes reduced in size compared with their free-living close relatives. Thus, the body louse genome project offers unique information and tools to use in advancing understanding of coevolution among vectors, symbionts, and pathogens.
Science | 2014
Víctor Soria-Carrasco; Zachariah Gompert; Aaron A. Comeault; Timothy E. Farkas; Thomas L. Parchman; J. Spencer Johnston; C. Alex Buerkle; Jeffrey L. Feder; Jens Bast; Tanja Schwander; Scott P. Egan; Bernard J. Crespi; Patrik Nosil
Stick to the Bush Can the underlying genetic changes driving the divergence of populations into new species be predicted or repeated? Soria-Carrasco et al. (p. 738) investigated the genetic changes observed after one generation when stick insect (Timema cristinae) populations were transplanted from their preferred host plants to alternative hosts. Diverged genetic regions were relatively small, with most loci showing divergence in a single population pair. However, the number of loci showing parallel divergence was greater than expected by chance. Thus, selection can drive parallel phenotypic evolution via parallel genetic changes. Parallel speciation in insects shows both convergent and divergent selection after one generation. Natural selection can drive the repeated evolution of reproductive isolation, but the genomic basis of parallel speciation remains poorly understood. We analyzed whole-genome divergence between replicate pairs of stick insect populations that are adapted to different host plants and undergoing parallel speciation. We found thousands of modest-sized genomic regions of accentuated divergence between populations, most of which are unique to individual population pairs. We also detected parallel genomic divergence across population pairs involving an excess of coding genes with specific molecular functions. Regions of parallel genomic divergence in nature exhibited exceptional allele frequency changes between hosts in a field transplant experiment. The results advance understanding of biological diversification by providing convergent observational and experimental evidence for selection’s role in driving repeatable genomic divergence.
PLOS ONE | 2011
Simon W. Baxter; John W. Davey; J. Spencer Johnston; Anthony M. Shelton; David G. Heckel; Chris D. Jiggins; Mark Blaxter
Restriction-site associated DNA (RAD) sequencing is a powerful new method for targeted sequencing across the genomes of many individuals. This approach has broad potential for genetic analysis of non-model organisms including genotype-phenotype association mapping, phylogeography, population genetics and scaffolding genome assemblies through linkage mapping. We constructed a RAD library using genomic DNA from a Plutella xylostella (diamondback moth) backcross that segregated for resistance to the insecticide spinosad. Sequencing of 24 individuals was performed on a single Illumina GAIIx lane (51 base paired-end reads). Taking advantage of the lack of crossing over in homologous chromosomes in female Lepidoptera, 3,177 maternally inherited RAD alleles were assigned to the 31 chromosomes, enabling identification of the spinosad resistance and W/Z sex chromosomes. Paired-end reads for each RAD allele were assembled into contigs and compared to the genome of Bombyx mori (n = 28) using BLAST, revealing 28 homologous matches plus 3 expected fusion/breakage events which account for the difference in chromosome number. A genome-wide linkage map (1292 cM) was inferred with 2,878 segregating RAD alleles inherited from the backcross father, producing chromosome and location specific sequenced RAD markers. Here we have used RAD sequencing to construct a genetic linkage map de novo for an organism that has no previous genome data. Comparative analysis of P. xyloxtella linkage groups with B. mori chromosomes shows for the first time, genetic synteny appears common beyond the Macrolepidoptera. RAD sequencing is a powerful system capable of rapidly generating chromosome specific data for non-model organisms.
Genome Research | 2014
Wen Huang; Andreas Massouras; Yutaka Inoue; Jason A. Peiffer; Miquel Ràmia; Aaron M. Tarone; Lavanya Turlapati; Thomas Zichner; Dianhui Zhu; Richard F. Lyman; Michael M. Magwire; Kerstin P. Blankenburg; Mary Anna Carbone; Kyle Chang; Lisa L. Ellis; Sonia Fernandez; Yi Han; Gareth Highnam; Carl E. Hjelmen; John Jack; Mehwish Javaid; Joy Jayaseelan; Divya Kalra; Sandy Lee; Lora Lewis; Mala Munidasa; Fiona Ongeri; Shohba Patel; Lora Perales; Agapito Perez
The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify 4,853,802 single nucleotide polymorphisms (SNPs) and 1,296,080 non-SNP variants. Our molecular population genomic analyses show higher deletion than insertion mutation rates and stronger purifying selection on deletions. Weaker selection on insertions than deletions is consistent with our observed distribution of genome size determined by flow cytometry, which is skewed toward larger genomes. Insertion/deletion and single nucleotide polymorphisms are positively correlated with each other and with local recombination, suggesting that their nonrandom distributions are due to hitchhiking and background selection. Our cytogenetic analysis identified 16 polymorphic inversions in the DGRP. Common inverted and standard karyotypes are genetically divergent and account for most of the variation in relatedness among the DGRP lines. Intriguingly, variation in genome size and many quantitative traits are significantly associated with inversions. Approximately 50% of the DGRP lines are infected with Wolbachia, and four lines have germline insertions of Wolbachia sequences, but effects of Wolbachia infection on quantitative traits are rarely significant. The DGRP complements ongoing efforts to functionally annotate the Drosophila genome. Indeed, 15% of all D. melanogaster genes segregate for potentially damaged proteins in the DGRP, and genome-wide analyses of quantitative traits identify novel candidate genes. The DGRP lines, sequence data, genotypes, quality scores, phenotypes, and analysis and visualization tools are publicly available.
Science | 2015
Karen M. Kapheim; Hailin Pan; Cai Li; Daniela Puiu; Tanja Magoc; Hugh M. Robertson; Matthew E. Hudson; Aarti Venkat; Brielle J. Fischman; Alvaro G. Hernandez; Mark Yandell; Daniel Ence; Carson Holt; George D. Yocum; William P. Kemp; Jordi Bosch; Robert M. Waterhouse; Evgeny M. Zdobnov; Eckart Stolle; F. Bernhard Kraus; Sophie Helbing; Robin F. A. Moritz; Karl M. Glastad; Brendan G. Hunt; Michael A. D. Goodisman; Frank Hauser; Cornelis J. P. Grimmelikhuijzen; Daniel G. Pinheiro; Francis Morais Franco Nunes; Michelle Soares
For bees, many roads lead to social harmony Eusociality, where workers sacrifice their reproductive rights to support the colony, has evolved repeatedly and represents the most evolved form of social evolution in insects. Kapheim et al. looked across the genomes of 10 bee species with varying degrees of sociality to determine the underlying genomic contributions. No one genomic path led to eusociality, but similarities across genomes were seen in features such as increases in gene regulation and methylation. It also seems that selection pressures relaxed after the emergence of complex sociality. Science, this issue p. 1139 Social evolution in bees has followed diverse genomic paths but shares genomic patterns. The evolution of eusociality is one of the major transitions in evolution, but the underlying genomic changes are unknown. We compared the genomes of 10 bee species that vary in social complexity, representing multiple independent transitions in social evolution, and report three major findings. First, many important genes show evidence of neutral evolution as a consequence of relaxed selection with increasing social complexity. Second, there is no single road map to eusociality; independent evolutionary transitions in sociality have independent genetic underpinnings. Third, though clearly independent in detail, these transitions do have similar general features, including an increase in constrained protein evolution accompanied by increases in the potential for gene regulation and decreases in diversity and abundance of transposable elements. Eusociality may arise through different mechanisms each time, but would likely always involve an increase in the complexity of gene networks.
Genetica | 2002
Jonathan F. Wendel; Richard Cronn; J. Spencer Johnston; H. James Price
Plant genomes vary over several orders of magnitude in size, even among closely related species, yet the origin, genesis and significance of this variation are not clear. Because DNA content varies over a sevenfold range among diploid species in the cotton genus (Gossypium) and its allies, this group offers opportunities for exploring patterns and mechanisms of genome size evolution. For example, the question has been raised whether plant genomes have a ‘one-way ticket to genomic obesity’, as a consequence of retroelement accumulation. Few empirical studies directly address this possibility, although it is consistent with recent insights gleaned from evolutionary genomic investigations. We used a phylogenetic approach to evaluate the directionality of genome size evolution among Gossypium species and their relatives in the cotton tribe (Gossypieae, Malvaceae). Our results suggest that both DNA content increase and decrease have occurred repeatedly during evolution. In contrast to a model of unidirectional genome size change, the frequency of inferred genome size contraction exceeded that of expansion. In conjunction with other evidence, this finding highlights the dynamic nature of plant genome size evolution, and suggests that poorly understood genomic contraction mechanisms operate on a more extensive scale that previously recognized. Moreover, the research sets the stage for fine-scale analysis of the evolutionary dynamics and directionality of change for the full spectrum of genomic constituents.
BMC Evolutionary Biology | 2008
Neil D. Tsutsui; Andrew V. Suarez; Joseph C. Spagna; J. Spencer Johnston
BackgroundDespite the economic and ecological importance of ants, genomic tools for this family (Formicidae) remain woefully scarce. Knowledge of genome size, for example, is a useful and necessary prerequisite for the development of many genomic resources, yet it has been reported for only one ant species (Solenopsis invicta), and the two published estimates for this species differ by 146.7 Mb (0.15 pg).ResultsHere, we report the genome size for 40 species of ants distributed across 10 of the 20 currently recognized subfamilies, thus making Formicidae the 4th most surveyed insect family and elevating the Hymenoptera to the 5th most surveyed insect order. Our analysis spans much of the ant phylogeny, from the less derived Amblyoponinae and Ponerinae to the more derived Myrmicinae, Formicinae and Dolichoderinae. We include a number of interesting and important taxa, including the invasive Argentine ant (Linepithema humile), Neotropical army ants (genera Eciton and Labidus), trapjaw ants (Odontomachus), fungus-growing ants (Apterostigma, Atta and Sericomyrmex), harvester ants (Messor, Pheidole and Pogonomyrmex), carpenter ants (Camponotus), a fire ant (Solenopsis), and a bulldog ant (Myrmecia). Our results show that ants possess small genomes relative to most other insects, yet genome size varies three-fold across this insect family. Moreover, our data suggest that two whole-genome duplications may have occurred in the ancestors of the modern Ectatomma and Apterostigma. Although some previous studies of other taxa have revealed a relationship between genome size and body size, our phylogenetically-controlled analysis of this correlation did not reveal a significant relationship.ConclusionThis is the first analysis of genome size in ants (Formicidae) and the first across multiple species of social insects. We show that genome size is a variable trait that can evolve gradually over long time spans, as well as rapidly, through processes that may include occasional whole-genome duplication. The small genome sizes of ants, combined with their ecological, evolutionary and agricultural importance, suggest that some of these species may be good candidates for future whole-genome sequencing projects.
Nature Communications | 2016
Joshua B. Benoit; Zach N. Adelman; Klaus Reinhardt; Amanda Dolan; Monica Poelchau; Emily C. Jennings; Elise M. Szuter; Richard W. Hagan; Hemant Gujar; Jayendra Nath Shukla; Fang Zhu; M. Mohan; David R. Nelson; Andrew J. Rosendale; Christian Derst; Valentina Resnik; Sebastian Wernig; Pamela Menegazzi; Christian Wegener; Nicolai Peschel; Jacob M. Hendershot; Wolfgang Blenau; Reinhard Predel; Paul R. Johnston; Panagiotis Ioannidis; Robert M. Waterhouse; Ralf Nauen; Corinna Schorn; Mark Christoph Ott; Frank Maiwald
The bed bug, Cimex lectularius, has re-established itself as a ubiquitous human ectoparasite throughout much of the world during the past two decades. This global resurgence is likely linked to increased international travel and commerce in addition to widespread insecticide resistance. Analyses of the C. lectularius sequenced genome (650 Mb) and 14,220 predicted protein-coding genes provide a comprehensive representation of genes that are linked to traumatic insemination, a reduced chemosensory repertoire of genes related to obligate hematophagy, host–symbiont interactions, and several mechanisms of insecticide resistance. In addition, we document the presence of multiple putative lateral gene transfer events. Genome sequencing and annotation establish a solid foundation for future research on mechanisms of insecticide resistance, human–bed bug and symbiont–bed bug associations, and unique features of bed bug biology that contribute to the unprecedented success of C. lectularius as a human ectoparasite.
Genome Biology | 2016
Duane D. McKenna; Erin D. Scully; Yannick Pauchet; Kelli Hoover; Roy Kirsch; Scott M. Geib; Robert F. Mitchell; Robert M. Waterhouse; Seung Joon Ahn; Deanna Arsala; Joshua B. Benoit; Heath Blackmon; Tiffany Bledsoe; Julia H. Bowsher; André Busch; Bernarda Calla; Hsu Chao; Anna K. Childers; Christopher Childers; Dave J. Clarke; Lorna Cohen; Jeffery P. Demuth; Huyen Dinh; HarshaVardhan Doddapaneni; Amanda Dolan; Jian J. Duan; Shannon Dugan; Markus Friedrich; Karl M. Glastad; Michael A. D. Goodisman
BackgroundRelatively little is known about the genomic basis and evolution of wood-feeding in beetles. We undertook genome sequencing and annotation, gene expression assays, studies of plant cell wall degrading enzymes, and other functional and comparative studies of the Asian longhorned beetle, Anoplophora glabripennis, a globally significant invasive species capable of inflicting severe feeding damage on many important tree species. Complementary studies of genes encoding enzymes involved in digestion of woody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 additional insects, including the newly sequenced emerald ash borer and bull-headed dung beetle.ResultsThe Asian longhorned beetle genome encodes a uniquely diverse arsenal of enzymes that can degrade the main polysaccharide networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woody plants. It has the metabolic plasticity needed to feed on diverse plant species, contributing to its highly invasive nature. Large expansions of chemosensory genes involved in the reception of pheromones and plant kairomones are consistent with the complexity of chemical cues it uses to find host plants and mates.ConclusionsAmplification and functional divergence of genes associated with specialized feeding on plants, including genes originally obtained via horizontal gene transfer from fungi and bacteria, contributed to the addition, expansion, and enhancement of the metabolic repertoire of the Asian longhorned beetle, certain other phytophagous beetles, and to a lesser degree, other phytophagous insects. Our results thus begin to establish a genomic basis for the evolutionary success of beetles on plants.