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Featured researches published by Christine G. Elsik.


Science | 2009

The Genome Sequence of Taurine Cattle : A Window to Ruminant Biology and Evolution

Christine G. Elsik; Ross L. Tellam; Kim C. Worley

A survey of genetic diversity of cattle suggests two domestication events in Asia and selection by husbandry. Not Just Dinner on Legs Several thousand years ago, human beings realized the virtues of domesticating wild animals as easy meat. Soon other possibilities became apparent, and as revealed in a series of papers in this issue, early pastoralists became selective about breeding for wool, leather, milk, and muscle power. In two papers, Gibbs et al. report on the bovine genome sequence (p. 522; see the cover, the Perspective by Lewin, and the Policy Forum by Roberts) and trace the diversity and genetic history of cattle (p. 528), while Chessa et al. (p. 532) survey the occurrence of endogenous retroviruses in sheep and map their distribution to historical waves of human selection and dispersal across Europe. Finally, Ludwig et al. (p. 485) note the origins of variation in the coat-color of horses and suggest that it is most likely to have been selected for by humans in need of good-looking transport. To understand the biology and evolution of ruminants, the cattle genome was sequenced to about sevenfold coverage. The cattle genome contains a minimum of 22,000 genes, with a core set of 14,345 orthologs shared among seven mammalian species of which 1217 are absent or undetected in noneutherian (marsupial or monotreme) genomes. Cattle-specific evolutionary breakpoint regions in chromosomes have a higher density of segmental duplications, enrichment of repetitive elements, and species-specific variations in genes associated with lactation and immune responsiveness. Genes involved in metabolism are generally highly conserved, although five metabolic genes are deleted or extensively diverged from their human orthologs. The cattle genome sequence thus provides a resource for understanding mammalian evolution and accelerating livestock genetic improvement for milk and meat production.


The Plant Cell | 2000

Comparative genomics of plant chromosomes

Andrew H. Paterson; John E. Bowers; Mark D. Burow; Xavier Draye; Christine G. Elsik; Chun-Xiao Jiang; Catherine S. Katsar; Tien-Hung Lan; Yann-Rong Lin; Reiguang Ming; Robert J. Wright

Comparative genomics, the study of similarities and differences in structure and function of the hereditary information in different taxa, uses molecular tools to investigate notions that far preceded the discovery that DNA was the hereditary molecule. Vavilov’s (1922) “law of homologous series in variation” was an early suggestion of the possibility of underlying commonality in the genetic blueprints of different (plant) species. In plants, genetic analysis based upon morphological and isozyme markers provided early hints that the arrangements of genes along the chromosomes of various taxa may have retained parallels since their divergence from common ancestors. DNA-level investigations in diverse taxa point to two broad messages: (1) The small but essential portion of most plant genomes encoding genes evolves relatively slowly, with corresponding genes retaining recognizable DNA sequences and similar order along the chromosomes of taxa that have been reproductively-isolated for millions of years. (2) A wide range of factors, such as DNA sequence mobility, gene deletion, and localized rearrangements, are superimposed on the relatively slow tempo of chromosomal evolution and cause many deviations from co-linearity. (3) Genetic loci that account for common phenotypes in different taxa are often at corresponding genomic locations, and may represent orthologous genes or members of orthologous clusters of genes.


Genome Biology | 2007

Creating a honey bee consensus gene set

Christine G. Elsik; Aaron J. Mackey; Justin T. Reese; Natalia V. Milshina; David S. Roos; George M. Weinstock

BackgroundWe wished to produce a single reference gene set for honey bee (Apis mellifera). Our motivation was twofold. First, we wished to obtain an improved set of gene models with increased coverage of known genes, while maintaining gene model quality. Second, we wished to provide a single official gene list that the research community could further utilize for consistent and comparable analyses and functional annotation.ResultsWe created a consensus gene set for honey bee (Apis mellifera) using GLEAN, a new algorithm that uses latent class analysis to automatically combine disparate gene prediction evidence in the absence of known genes. The consensus gene models had increased representation of honey bee genes without sacrificing quality compared with any one of the input gene predictions. When compared with manually annotated gold standards, the consensus set of gene models was similar or superior in quality to each of the input sets.ConclusionMost eukaryotic genome projects produce multiple gene sets because of the variety of gene prediction programs. Each of the gene prediction programs has strengths and weaknesses, and so the multiplicity of gene sets offers users a more comprehensive collection of genes to use than is available from a single program. On the other hand, the availability of multiple gene sets is also a cause for uncertainty among users as regards which set they should use. GLEAN proved to be an effective method to combine gene lists into a single reference set.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Draft genome of the globally widespread and invasive Argentine ant (Linepithema humile)

Christopher D. Smith; Aleksey V. Zimin; Carson Holt; Ehab Abouheif; Richard Benton; Elizabeth Cash; Vincent Croset; Cameron R. Currie; Eran Elhaik; Christine G. Elsik; Marie Julie Favé; Vilaiwan Fernandes; Jürgen Gadau; Joshua D. Gibson; Dan Graur; Kirk J. Grubbs; Darren E. Hagen; Martin Helmkampf; Jo Anne Holley; Hao Hu; Ana Sofia Ibarraran Viniegra; Brian R. Johnson; Reed M. Johnson; Abderrahman Khila; Jay W. Kim; Joseph G. Laird; Kaitlyn A. Mathis; Joseph A. Moeller; Monica Munoz-Torres; Marguerite C. Murphy

Ants are some of the most abundant and familiar animals on Earth, and they play vital roles in most terrestrial ecosystems. Although all ants are eusocial, and display a variety of complex and fascinating behaviors, few genomic resources exist for them. Here, we report the draft genome sequence of a particularly widespread and well-studied species, the invasive Argentine ant (Linepithema humile), which was accomplished using a combination of 454 (Roche) and Illumina sequencing and community-based funding rather than federal grant support. Manual annotation of >1,000 genes from a variety of different gene families and functional classes reveals unique features of the Argentine ants biology, as well as similarities to Apis mellifera and Nasonia vitripennis. Distinctive features of the Argentine ant genome include remarkable expansions of gustatory (116 genes) and odorant receptors (367 genes), an abundance of cytochrome P450 genes (>110), lineage-specific expansions of yellow/major royal jelly proteins and desaturases, and complete CpG DNA methylation and RNAi toolkits. The Argentine ant genome contains fewer immune genes than Drosophila and Tribolium, which may reflect the prominent role played by behavioral and chemical suppression of pathogens. Analysis of the ratio of observed to expected CpG nucleotides for genes in the reproductive development and apoptosis pathways suggests higher levels of methylation than in the genome overall. The resources provided by this genome sequence will offer an abundance of tools for researchers seeking to illuminate the fascinating biology of this emerging model organism.


PLOS Genetics | 2011

The Genome Sequence of the Leaf-Cutter Ant Atta cephalotes Reveals Insights into Its Obligate Symbiotic Lifestyle

Garret Suen; Clotilde Teiling; Lewyn Li; Carson Holt; Ehab Abouheif; Erich Bornberg-Bauer; Pascal Bouffard; Eric J. Caldera; Elizabeth Cash; Amy Cavanaugh; Olgert Denas; Eran Elhaik; Marie-Julie Favé; Jürgen Gadau; Joshua D. Gibson; Dan Graur; Kirk J. Grubbs; Darren E. Hagen; Timothy T. Harkins; Martin Helmkampf; Hao Hu; Brian R. Johnson; Jay Joong Kim; Sarah E. Marsh; Joseph A. Moeller; Monica Munoz-Torres; Marguerite C. Murphy; Meredith C. Naughton; Surabhi Nigam; Rick P. Overson

Leaf-cutter ants are one of the most important herbivorous insects in the Neotropics, harvesting vast quantities of fresh leaf material. The ants use leaves to cultivate a fungus that serves as the colonys primary food source. This obligate ant-fungus mutualism is one of the few occurrences of farming by non-humans and likely facilitated the formation of their massive colonies. Mature leaf-cutter ant colonies contain millions of workers ranging in size from small garden tenders to large soldiers, resulting in one of the most complex polymorphic caste systems within ants. To begin uncovering the genomic underpinnings of this system, we sequenced the genome of Atta cephalotes using 454 pyrosequencing. One prediction from this ants lifestyle is that it has undergone genetic modifications that reflect its obligate dependence on the fungus for nutrients. Analysis of this genome sequence is consistent with this hypothesis, as we find evidence for reductions in genes related to nutrient acquisition. These include extensive reductions in serine proteases (which are likely unnecessary because proteolysis is not a primary mechanism used to process nutrients obtained from the fungus), a loss of genes involved in arginine biosynthesis (suggesting that this amino acid is obtained from the fungus), and the absence of a hexamerin (which sequesters amino acids during larval development in other insects). Following recent reports of genome sequences from other insects that engage in symbioses with beneficial microbes, the A. cephalotes genome provides new insights into the symbiotic lifestyle of this ant and advances our understanding of host–microbe symbioses.


BMC Genomics | 2014

Finding the missing honey bee genes: Lessons learned from a genome upgrade

Christine G. Elsik; Kim C. Worley; Anna K. Bennett; Martin Beye; Francisco Camara; Christopher P. Childers; Dirk C. de Graaf; Griet Debyser; Jixin Deng; Bart Devreese; Eran Elhaik; Jay D. Evans; Leonard J. Foster; Dan Graur; Roderic Guigó; Katharina Hoff; Michael Holder; Matthew E. Hudson; Greg J. Hunt; Huaiyang Jiang; Vandita Joshi; Radhika S. Khetani; Peter Kosarev; Christie Kovar; Jian Ma; Ryszard Maleszka; Robin F. A. Moritz; Monica Munoz-Torres; Terence Murphy; Donna M. Muzny

BackgroundThe first generation of genome sequence assemblies and annotations have had a significant impact upon our understanding of the biology of the sequenced species, the phylogenetic relationships among species, the study of populations within and across species, and have informed the biology of humans. As only a few Metazoan genomes are approaching finished quality (human, mouse, fly and worm), there is room for improvement of most genome assemblies. The honey bee (Apis mellifera) genome, published in 2006, was noted for its bimodal GC content distribution that affected the quality of the assembly in some regions and for fewer genes in the initial gene set (OGSv1.0) compared to what would be expected based on other sequenced insect genomes.ResultsHere, we report an improved honey bee genome assembly (Amel_4.5) with a new gene annotation set (OGSv3.2), and show that the honey bee genome contains a number of genes similar to that of other insect genomes, contrary to what was suggested in OGSv1.0. The new genome assembly is more contiguous and complete and the new gene set includes ~5000 more protein-coding genes, 50% more than previously reported. About 1/6 of the additional genes were due to improvements to the assembly, and the remaining were inferred based on new RNAseq and protein data.ConclusionsLessons learned from this genome upgrade have important implications for future genome sequencing projects. Furthermore, the improvements significantly enhance genomic resources for the honey bee, a key model for social behavior and essential to global ecology through pollination.


Nucleic Acids Research | 2011

Hymenoptera Genome Database: integrated community resources for insect species of the order Hymenoptera

Monica Munoz-Torres; Justin T. Reese; Christopher P. Childers; Anna K. Bennett; Jaideep P. Sundaram; Kevin L. Childs; Juan M. Anzola; Natalia V. Milshina; Christine G. Elsik

The Hymenoptera Genome Database (HGD) is a comprehensive model organism database that caters to the needs of scientists working on insect species of the order Hymenoptera. This system implements open-source software and relational databases providing access to curated data contributed by an extensive, active research community. HGD contains data from 9 different species across ∼200 million years in the phylogeny of Hymenoptera, allowing researchers to leverage genetic, genome sequence and gene expression data, as well as the biological knowledge of related model organisms. The availability of resources across an order greatly facilitates comparative genomics and enhances our understanding of the biology of agriculturally important Hymenoptera species through genomics. Curated data at HGD includes predicted and annotated gene sets supported with evidence tracks such as ESTs/cDNAs, small RNA sequences and GC composition domains. Data at HGD can be queried using genome browsers and/or BLAST/PSI-BLAST servers, and it may also be downloaded to perform local searches. We encourage the public to access and contribute data to HGD at: http://HymenopteraGenome.org.


BioMed Research International | 2010

Development and application of bovine and porcine oligonucleotide arrays with protein-based annotation.

John R. Garbe; Christine G. Elsik; Eric Antoniou; James M. Reecy; Karl J. Clark; Anand Venkatraman; JaeWoo Kim; Robert D. Schnabel; C. Michael Dickens; Russell D. Wolfinger; Scott C. Fahrenkrug; Jeremy F. Taylor

The design of oligonucleotide sequences for the detection of gene expression in species with disparate volumes of genome and EST sequence information has been broadly studied. However, a congruous strategy has yet to emerge to allow the design of sensitive and specific gene expression detection probes. This study explores the use of a phylogenomic approach to align transcribed sequences to vertebrate protein sequences for the detection of gene families to design genomewide 70-mer oligonucleotide probe sequences for bovine and porcine. The bovine array contains 23,580 probes that target the transcripts of 16,341 genes, about 72% of the total number of bovine genes. The porcine array contains 19,980 probes targeting 15,204 genes, about 76% of the genes in the Ensembl annotation of the pig genome. An initial experiment using the bovine array demonstrates the specificity and sensitivity of the array.


Genome Biology | 2010

The pea aphid genome sequence brings theories of insect defense into question

Christine G. Elsik

The genome sequence of the pea aphid is the first for a basal hemimetabolous insect and provides insights into developmental plasticity, symbiosis and insect immunity.


Physiological Genomics | 2009

Discovery of candidate genes and pathways in the endometrium regulating ovine blastocyst growth and conceptus elongation

M. Carey Satterfield; Gwonhwa Song; Kelli J. Kochan; Penny K. Riggs; Rebecca M. Simmons; Christine G. Elsik; David L. Adelson; Fuller W. Bazer; Huaijun Zhou; Thomas E. Spencer

Establishment of pregnancy in ruminants requires blastocyst growth to form an elongated conceptus that produces interferon tau, the pregnancy recognition signal, and initiates implantation. Blastocyst growth and development requires secretions from the uterine endometrium. An early increase in circulating concentrations of progesterone (P4) stimulates blastocyst growth and elongation in ruminants. This study utilized sheep as a model to identify candidate genes and regulatory networks in the endometrium that govern preimplantation blastocyst growth and development. Ewes were treated daily with either P4 or corn oil vehicle from day 1.5 after mating to either day 9 or day 12 of pregnancy when endometrium was obtained by hysterectomy. Microarray analyses revealed many differentially expressed genes in the endometria affected by day of pregnancy and early P4 treatment. In situ hybridization analyses revealed that many differentially expressed genes were expressed in a cell-specific manner within the endometrium. The Database for Annotation, Visualization, and Integrated Discovery (DAVID) was used to identify functional groups of genes and biological processes in the endometrium that are associated with growth and development of preimplantation blastocysts. Notably, biological processes affected by day of pregnancy and/or early P4 treatment included lipid biosynthesis and metabolism, angiogenesis, transport, extracellular space, defense and inflammatory response, proteolysis, amino acid transport and metabolism, and hormone metabolism. This transcriptomic data provides novel insights into the biology of endometrial function and preimplantation blastocyst growth and development in sheep.

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Monica Munoz-Torres

Lawrence Berkeley National Laboratory

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Kevin L. Childs

Michigan State University

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Kim C. Worley

Baylor College of Medicine

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Dan Graur

University of Houston

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