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Dive into the research topics where David A. Ray is active.

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Featured researches published by David A. Ray.


Nature | 2012

Butterfly genome reveals promiscuous exchange of mimicry adaptations among species

Kanchon K. Dasmahapatra; James R. Walters; Adriana D. Briscoe; John W. Davey; Annabel Whibley; Nicola J. Nadeau; Aleksey V. Zimin; Daniel S.T. Hughes; Laura Ferguson; Simon H. Martin; Camilo Salazar; James J. Lewis; Sebastian Adler; Seung-Joon Ahn; Dean A. Baker; Simon W. Baxter; Nicola Chamberlain; Ritika Chauhan; Brian A. Counterman; Tamas Dalmay; Lawrence E. Gilbert; Karl H.J. Gordon; David G. Heckel; Heather M. Hines; Katharina Hoff; Peter W. H. Holland; Emmanuelle Jacquin-Joly; Francis M. Jiggins; Robert T. Jones; Durrell D. Kapan

The evolutionary importance of hybridization and introgression has long been debated. Hybrids are usually rare and unfit, but even infrequent hybridization can aid adaptation by transferring beneficial traits between species. Here we use genomic tools to investigate introgression in Heliconius, a rapidly radiating genus of neotropical butterflies widely used in studies of ecology, behaviour, mimicry and speciation. We sequenced the genome of Heliconius melpomene and compared it with other taxa to investigate chromosomal evolution in Lepidoptera and gene flow among multiple Heliconius species and races. Among 12,669 predicted genes, biologically important expansions of families of chemosensory and Hox genes are particularly noteworthy. Chromosomal organization has remained broadly conserved since the Cretaceous period, when butterflies split from the Bombyx (silkmoth) lineage. Using genomic resequencing, we show hybrid exchange of genes between three co-mimics, Heliconius melpomene, Heliconius timareta and Heliconius elevatus, especially at two genomic regions that control mimicry pattern. We infer that closely related Heliconius species exchange protective colour-pattern genes promiscuously, implying that hybridization has an important role in adaptive radiation.


Nature | 2011

The genome of the green anole lizard and a comparative analysis with birds and mammals

Jessica Alföldi; Federica Di Palma; Manfred Grabherr; Christina Williams; Lesheng Kong; Evan Mauceli; Pamela Russell; Craig B. Lowe; Richard E. Glor; Jacob D. Jaffe; David A. Ray; Stéphane Boissinot; Andrew M. Shedlock; Todd A. Castoe; John K. Colbourne; Matthew K. Fujita; Ricardo Moreno; Boudewijn ten Hallers; David Haussler; Andreas Heger; David I. Heiman; Daniel E. Janes; Jeremy Johnson; Pieter J. de Jong; Maxim Koriabine; Marcia Lara; Peter Novick; Chris L. Organ; Sally E. Peach; Steven Poe

The evolution of the amniotic egg was one of the great evolutionary innovations in the history of life, freeing vertebrates from an obligatory connection to water and thus permitting the conquest of terrestrial environments. Among amniotes, genome sequences are available for mammals and birds, but not for non-avian reptiles. Here we report the genome sequence of the North American green anole lizard, Anolis carolinensis. We find that A. carolinensis microchromosomes are highly syntenic with chicken microchromosomes, yet do not exhibit the high GC and low repeat content that are characteristic of avian microchromosomes. Also, A. carolinensis mobile elements are very young and diverse—more so than in any other sequenced amniote genome. The GC content of this lizard genome is also unusual in its homogeneity, unlike the regionally variable GC content found in mammals and birds. We describe and assign sequence to the previously unknown A. carolinensis X chromosome. Comparative gene analysis shows that amniote egg proteins have evolved significantly more rapidly than other proteins. An anole phylogeny resolves basal branches to illuminate the history of their repeated adaptive radiations.


Science | 2014

Comparative genomics reveals insights into avian genome evolution and adaptation

Guojie Zhang; Cai Li; Qiye Li; Bo Li; Denis M. Larkin; Chul Hee Lee; Jay F. Storz; Agostinho Antunes; Matthew J. Greenwold; Robert W. Meredith; Qi Zhou; Luohao Xu; Zongji Wang; Pei Zhang; Haofu Hu; Wei Yang; Jiang Hu; Jin Xiao; Zhikai Yang; Yang Liu; Qiaolin Xie; Hao Yu; Jinmin Lian; Ping Wen; Fang Zhang; Hui Li; Yongli Zeng; Zijun Xiong; Shiping Liu; Zhiyong Huang

Birds are the most species-rich class of tetrapod vertebrates and have wide relevance across many research fields. We explored bird macroevolution using full genomes from 48 avian species representing all major extant clades. The avian genome is principally characterized by its constrained size, which predominantly arose because of lineage-specific erosion of repetitive elements, large segmental deletions, and gene loss. Avian genomes furthermore show a remarkably high degree of evolutionary stasis at the levels of nucleotide sequence, gene synteny, and chromosomal structure. Despite this pattern of conservation, we detected many non-neutral evolutionary changes in protein-coding genes and noncoding regions. These analyses reveal that pan-avian genomic diversity covaries with adaptations to different lifestyles and convergent evolution of traits.


Proceedings of the National Academy of Sciences of the United States of America | 2013

The Burmese python genome reveals the molecular basis for extreme adaptation in snakes

Todd A. Castoe; A. P. Jason de Koning; Kathryn T. Hall; Daren C. Card; Drew R. Schield; Matthew K. Fujita; Robert P. Ruggiero; Jack F. Degner; Juan M. Daza; Wanjun Gu; Jacobo Reyes-Velasco; Kyle J. Shaney; Jill M. Castoe; Samuel E. Fox; Alex W. Poole; Daniel Polanco; Jason Dobry; Michael W. Vandewege; Qing Li; Ryan K. Schott; Aurélie Kapusta; Patrick Minx; Cédric Feschotte; Peter Uetz; David A. Ray; Federico G. Hoffmann; Robert Bogden; Eric N. Smith; Belinda S. W. Chang; Freek J. Vonk

Significance The molecular basis of morphological and physiological adaptations in snakes is largely unknown. Here, we study these phenotypes using the genome of the Burmese python (Python molurus bivittatus), a model for extreme phenotypic plasticity and metabolic adaptation. We discovered massive rapid changes in gene expression that coordinate major changes in organ size and function after feeding. Many significantly responsive genes are associated with metabolism, development, and mammalian diseases. A striking number of genes experienced positive selection in ancestral snakes. Such genes were related to metabolism, development, lungs, eyes, heart, kidney, and skeletal structure—all highly modified features in snakes. Snake phenotypic novelty seems to be driven by the system-wide coordination of protein adaptation, gene expression, and changes in genome structure. Snakes possess many extreme morphological and physiological adaptations. Identification of the molecular basis of these traits can provide novel understanding for vertebrate biology and medicine. Here, we study snake biology using the genome sequence of the Burmese python (Python molurus bivittatus), a model of extreme physiological and metabolic adaptation. We compare the python and king cobra genomes along with genomic samples from other snakes and perform transcriptome analysis to gain insights into the extreme phenotypes of the python. We discovered rapid and massive transcriptional responses in multiple organ systems that occur on feeding and coordinate major changes in organ size and function. Intriguingly, the homologs of these genes in humans are associated with metabolism, development, and pathology. We also found that many snake metabolic genes have undergone positive selection, which together with the rapid evolution of mitochondrial proteins, provides evidence for extensive adaptive redesign of snake metabolic pathways. Additional evidence for molecular adaptation and gene family expansions and contractions is associated with major physiological and phenotypic adaptations in snakes; genes involved are related to cell cycle, development, lungs, eyes, heart, intestine, and skeletal structure, including GRB2-associated binding protein 1, SSH, WNT16, and bone morphogenetic protein 7. Finally, changes in repetitive DNA content, guanine-cytosine isochore structure, and nucleotide substitution rates indicate major shifts in the structure and evolution of snake genomes compared with other amniotes. Phenotypic and physiological novelty in snakes seems to be driven by system-wide coordination of protein adaptation, gene expression, and changes in the structure of the genome.


Proceedings of the National Academy of Sciences of the United States of America | 2003

Alu elements and hominid phylogenetics

Abdel Halim Salem; David A. Ray; Jinchuan Xing; Pauline A. Callinan; Jeremy S. Myers; Dale J. Hedges; Randall K. Garber; David J. Witherspoon; Lynn B. Jorde; Mark A. Batzer

Alu elements have inserted in primate genomes throughout the evolution of the order. One particular Alu lineage (Ye) began amplifying relatively early in hominid evolution and continued propagating at a low level as many of its members are found in a variety of hominid genomes. This study represents the first conclusive application of short interspersed elements, which are considered nearly homoplasy-free, to elucidate the phylogeny of hominids. Phylogenetic analysis of Alu Ye5 elements and elements from several other subfamilies reveals high levels of support for monophyly of Hominidae, tribe Hominini and subtribe Hominina. Here we present the strongest evidence reported to date for a sister relationship between humans and chimpanzees while clearly distinguishing the chimpanzee and human lineages.


Science | 2014

Three crocodilian genomes reveal ancestral patterns of evolution among archosaurs

Richard E. Green; Edward L. Braun; Joel Armstrong; Dent Earl; Ngan Nguyen; Glenn Hickey; Michael W. Vandewege; John St. John; Salvador Capella-Gutiérrez; Todd A. Castoe; Colin Kern; Matthew K. Fujita; Juan C. Opazo; Jerzy Jurka; Kenji K. Kojima; Juan Caballero; Robert Hubley; Arian Smit; Roy N. Platt; Christine Lavoie; Meganathan P. Ramakodi; John W. Finger; Alexander Suh; Sally R. Isberg; Lee G. Miles; Amanda Y. Chong; Weerachai Jaratlerdsiri; Jaime Gongora; C. Moran; Andrés Iriarte

INTRODUCTION Crocodilians and birds are the two extant clades of archosaurs, a group that includes the extinct dinosaurs and pterosaurs. Fossils suggest that living crocodilians (alligators, crocodiles, and gharials) have a most recent common ancestor 80 to 100 million years ago. Extant crocodilians are notable for their distinct morphology, limited intraspecific variation, and slow karyotype evolution. Despite their unique biology and phylogenetic position, little is known about genome evolution within crocodilians. Evolutionary rates of tetrapods inferred from DNA sequences anchored by ultraconserved elements. Evolutionary rates among reptiles vary, with especially low rates among extant crocodilians but high rates among squamates. We have reconstructed the genomes of the common ancestor of birds and of all archosaurs (shown in gray silhouette, although the morphology of these species is uncertain). RATIONALE Genome sequences for the American alligator, saltwater crocodile, and Indian gharial—representatives of all three extant crocodilian families—were obtained to facilitate better understanding of the unique biology of this group and provide a context for studying avian genome evolution. Sequence data from these three crocodilians and birds also allow reconstruction of the ancestral archosaurian genome. RESULTS We sequenced shotgun genomic libraries from each species and used a variety of assembly strategies to obtain draft genomes for these three crocodilians. The assembled scaffold N50 was highest for the alligator (508 kilobases). Using a panel of reptile genome sequences, we generated phylogenies that confirm the sister relationship between crocodiles and gharials, the relationship with birds as members of extant Archosauria, and the outgroup status of turtles relative to birds and crocodilians. We also estimated evolutionary rates along branches of the tetrapod phylogeny using two approaches: ultraconserved element–anchored sequences and fourfold degenerate sites within stringently filtered orthologous gene alignments. Both analyses indicate that the rates of base substitution along the crocodilian and turtle lineages are extremely low. Supporting observations were made for transposable element content and for gene family evolution. Analysis of whole-genome alignments across a panel of reptiles and mammals showed that the rate of accumulation of micro-insertions and microdeletions is proportionally lower in crocodilians, consistent with a single underlying cause of a reduced rate of evolutionary change rather than intrinsic differences in base repair machinery. We hypothesize that this single cause may be a consistently longer generation time over the evolutionary history of Crocodylia. Low heterozygosity was observed in each genome, consistent with previous analyses, including the Chinese alligator. Pairwise sequential Markov chain analysis of regional heterozygosity indicates that during glacial cycles of the Pleistocene, each species suffered reductions in effective population size. The reduction was especially strong for the American alligator, whose current range extends farthest into regions of temperate climates. CONCLUSION We used crocodilian, avian, and outgroup genomes to reconstruct 584 megabases of the archosaurian common ancestor genome and the genomes of key ancestral nodes. The estimated accuracy of the archosaurian genome reconstruction is 91% and is higher for conserved regions such as genes. The reconstructed genome can be improved by adding more crocodilian and avian genome assemblies and may provide a unique window to the genomes of extinct organisms such as dinosaurs and pterosaurs. To provide context for the diversification of archosaurs—the group that includes crocodilians, dinosaurs, and birds—we generated draft genomes of three crocodilians: Alligator mississippiensis (the American alligator), Crocodylus porosus (the saltwater crocodile), and Gavialis gangeticus (the Indian gharial). We observed an exceptionally slow rate of genome evolution within crocodilians at all levels, including nucleotide substitutions, indels, transposable element content and movement, gene family evolution, and chromosomal synteny. When placed within the context of related taxa including birds and turtles, this suggests that the common ancestor of all of these taxa also exhibited slow genome evolution and that the comparatively rapid evolution is derived in birds. The data also provided the opportunity to analyze heterozygosity in crocodilians, which indicates a likely reduction in population size for all three taxa through the Pleistocene. Finally, these data combined with newly published bird genomes allowed us to reconstruct the partial genome of the common ancestor of archosaurs, thereby providing a tool to investigate the genetic starting material of crocodilians, birds, and dinosaurs.


Systematic Biology | 2006

SINEs of a Nearly Perfect Character

David A. Ray; Jinchuan Xing; Abdel Halim Salem; Mark A. Batzer

Mobile elements have been recognized as powerful tools for phylogenetic and population-level analyses. However, issues regarding potential sources of homoplasy and other misleading events have been raised. We have collected available data for all phylogenetic and population level studies of primates utilizing Alu insertion data and examined them for potentially homoplasious and other misleading events. Very low levels of each potential confounding factor in a phylogenetic or population analysis (i.e., lineage sorting, parallel insertions, and precise excision) were found. Although taxa known to be subject to high levels of these types of events may indeed be subject to problems when using SINE analysis, we propose that most taxa will respond as the order Primates has--by the resolution of several long-standing problems observed using sequence-based methods.


Genome Biology | 2012

Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes

John St. John; Edward L. Braun; Sally R. Isberg; Lee G. Miles; Amanda Yoon-Yee Chong; Jaime Gongora; Pauline Dalzell; C. Moran; Bertrand Bed'hom; Arhat Abzhanov; Shane C. Burgess; Amanda M. Cooksey; Todd A. Castoe; Nicholas G. Crawford; Llewellyn D. Densmore; Jennifer C. Drew; Scott V. Edwards; Brant C. Faircloth; Matthew K. Fujita; Matthew J. Greenwold; Federico G. Hoffmann; Jonathan M. Howard; Taisen Iguchi; Daniel E. Janes; Shahid Yar Khan; Satomi Kohno; A. P. Jason de Koning; Stacey L. Lance; Fiona M. McCarthy; John E. McCormack

The International Crocodilian Genomes Working Group (ICGWG) will sequence and assemble the American alligator (Alligator mississippiensis), saltwater crocodile (Crocodylus porosus) and Indian gharial (Gavialis gangeticus) genomes. The status of these projects and our planned analyses are described.


Genome Research | 2008

Multiple waves of recent DNA transposon activity in the bat, Myotis lucifugus

David A. Ray; Cédric Feschotte; Heidi J.T. Pagan; Jeremy D. Smith; Ellen J. Pritham; Peter Arensburger; Peter W. Atkinson; Nancy L. Craig

DNA transposons, or class 2 transposable elements, have successfully propagated in a wide variety of genomes. However, it is widely believed that DNA transposon activity has ceased in mammalian genomes for at least the last 40 million years. We recently reported evidence for the relatively recent activity of hAT and Helitron elements, two distinct groups of DNA transposons, in the lineage of the vespertilionid bat Myotis lucifugus. Here, we describe seven additional families that have also been recently active in the bat lineage. Early vespertilionid genome evolution was dominated by the activity of Helitrons, mariner-like and Tc2-like elements. This was followed by the colonization of Tc1-like elements, and by a more recent explosion of hAT-like elements. Finally, and most recently, piggyBac-like elements have amplified within the Myotis genome and our results indicate that one of these families is probably still expanding in natural populations. Together, these data suggest that there has been tremendous recent activity of various DNA transposons in the bat lineage that far exceeds those previously reported for any mammalian lineage. The diverse and recent populations of DNA transposons in genus Myotis will provide an unprecedented opportunity to study the impact of this class of elements on mammalian genome evolution and to better understand what makes some species more susceptible to invasion by genomic parasites than others.


Nature Communications | 2013

Draft genome sequence of the Tibetan antelope.

Ri-Li Ge; Qingle Cai; Yong-Yi Shen; A. san; Lan Ma; Yong Zhang; Xin Yi; Yan Chen; Lingfeng Yang; Ying Huang; Rongjun He; Yuanyuan Hui; Meirong Hao; Yue Li; Bo Wang; Xiaohua Ou; Jiaohui Xu; Yongfen Zhang; K ui Wu; Chunyu Geng; Wei-Ping Zhou; Taicheng Zhou; David M. Irwin; Yingzhong Yang; Liu Ying; Jaebum Kim; Denis M. Larkin; Jian Ma; Harris A. Lewin; Jinchuan Xing

The Tibetan antelope (Pantholops hodgsonii) is endemic to the extremely inhospitable high-altitude environment of the Qinghai-Tibetan Plateau, a region that has a low partial pressure of oxygen and high ultraviolet radiation. Here we generate a draft genome of this artiodactyl and use it to detect the potential genetic bases of highland adaptation. Compared with other plain-dwelling mammals, the genome of the Tibetan antelope shows signals of adaptive evolution and gene-family expansion in genes associated with energy metabolism and oxygen transmission. Both the highland American pika, and the Tibetan antelope have signals of positive selection for genes involved in DNA repair and the production of ATPase. Genes associated with hypoxia seem to have experienced convergent evolution. Thus, our study suggests that common genetic mechanisms might have been utilized to enable high-altitude adaptation.

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Mark A. Batzer

Louisiana State University

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Federico G. Hoffmann

Mississippi State University

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Michael W. Vandewege

Mississippi State University

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Todd A. Castoe

University of Texas at Arlington

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Jeremy D. Smith

Mississippi State University

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