Jiaxin Qu
Baylor College of Medicine
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Publication
Featured researches published by Jiaxin Qu.
Nature | 2012
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.
PLOS ONE | 2012
Adam C English; Stephen Richards; Yi Han; Min Wang; Vanesa Vee; Jiaxin Qu; Xiang Qin; Donna M. Muzny; Jeffrey G. Reid; Kim C. Worley; Richard A. Gibbs
Many genomes have been sequenced to high-quality draft status using Sanger capillary electrophoresis and/or newer short-read sequence data and whole genome assembly techniques. However, even the best draft genomes contain gaps and other imperfections due to limitations in the input data and the techniques used to build draft assemblies. Sequencing biases, repetitive genomic features, genomic polymorphism, and other complicating factors all come together to make some regions difficult or impossible to assemble. Traditionally, draft genomes were upgraded to “phase 3 finished” status using time-consuming and expensive Sanger-based manual finishing processes. For more facile assembly and automated finishing of draft genomes, we present here an automated approach to finishing using long-reads from the Pacific Biosciences RS (PacBio) platform. Our algorithm and associated software tool, PBJelly, (publicly available at https://sourceforge.net/projects/pb-jelly/) automates the finishing process using long sequence reads in a reference-guided assembly process. PBJelly also provides “lift-over” co-ordinate tables to easily port existing annotations to the upgraded assembly. Using PBJelly and long PacBio reads, we upgraded the draft genome sequences of a simulated Drosophila melanogaster, the version 2 draft Drosophila pseudoobscura, an assembly of the Assemblathon 2.0 budgerigar dataset, and a preliminary assembly of the Sooty mangabey. With 24× mapped coverage of PacBio long-reads, we addressed 99% of gaps and were able to close 69% and improve 12% of all gaps in D. pseudoobscura. With 4× mapped coverage of PacBio long-reads we saw reads address 63% of gaps in our budgerigar assembly, of which 32% were closed and 63% improved. With 6.8× mapped coverage of mangabey PacBio long-reads we addressed 97% of gaps and closed 66% of addressed gaps and improved 19%. The accuracy of gap closure was validated by comparison to Sanger sequencing on gaps from the original D. pseudoobscura draft assembly and shown to be dependent on initial reference quality.
Nature Genetics | 2015
Andrew D. Foote; Yue Liu; Gregg W.C. Thomas; Tomáš Vinař; Jessica Alföldi; Jixin Deng; Shannon Dugan; Cornelis E van Elk; Margaret E Hunter; Vandita Joshi; Ziad Khan; Christie Kovar; Sandra L. Lee; Kerstin Lindblad-Toh; Annalaura Mancia; Rasmus Nielsen; Xiang Qin; Jiaxin Qu; Brian J. Raney; Nagarjun Vijay; Jochen B. W. Wolf; Matthew W. Hahn; Donna M. Muzny; Kim C. Worley; M. Thomas P. Gilbert; Richard A. Gibbs
Marine mammals from different mammalian orders share several phenotypic traits adapted to the aquatic environment and therefore represent a classic example of convergent evolution. To investigate convergent evolution at the genomic level, we sequenced and performed de novo assembly of the genomes of three species of marine mammals (the killer whale, walrus and manatee) from three mammalian orders that share independently evolved phenotypic adaptations to a marine existence. Our comparative genomic analyses found that convergent amino acid substitutions were widespread throughout the genome and that a subset of these substitutions were in genes evolving under positive selection and putatively associated with a marine phenotype. However, we found higher levels of convergent amino acid substitutions in a control set of terrestrial sister taxa to the marine mammals. Our results suggest that, whereas convergent molecular evolution is relatively common, adaptive molecular convergence linked to phenotypic convergence is comparatively rare.
Current Biology | 2015
Chaoyang Zhao; Lucio Navarro Escalante; Hang Chen; Thiago R. Benatti; Jiaxin Qu; Sanjay Chellapilla; Robert M. Waterhouse; David Wheeler; Martin Andersson; Riyue Bao; Matthew Batterton; Susanta K. Behura; Kerstin P. Blankenburg; Doina Caragea; James C. Carolan; Marcus Coyle; Mustapha El-Bouhssini; Liezl Francisco; Markus Friedrich; Navdeep Gill; Tony Grace; Cornelis J. P. Grimmelikhuijzen; Yi Han; Frank Hauser; Nicolae Herndon; Michael Holder; Panagiotis Ioannidis; LaRonda Jackson; Mehwish Javaid; Shalini N. Jhangiani
Gall-forming arthropods are highly specialized herbivores that, in combination with their hosts, produce extended phenotypes with unique morphologies [1]. Many are economically important, and others have improved our understanding of ecology and adaptive radiation [2]. However, the mechanisms that these arthropods use to induce plant galls are poorly understood. We sequenced the genome of the Hessian fly (Mayetiola destructor; Diptera: Cecidomyiidae), a plant parasitic gall midge and a pest of wheat (Triticum spp.), with the aim of identifying genic modifications that contribute to its plant-parasitic lifestyle. Among several adaptive modifications, we discovered an expansive reservoir of potential effector proteins. Nearly 5% of the 20,163 predicted gene models matched putative effector gene transcripts present in the M. destructor larval salivary gland. Another 466 putative effectors were discovered among the genes that have no sequence similarities in other organisms. The largest known arthropod gene family (family SSGP-71) was also discovered within the effector reservoir. SSGP-71 proteins lack sequence homologies to other proteins, but their structures resemble both ubiquitin E3 ligases in plants and E3-ligase-mimicking effectors in plant pathogenic bacteria. SSGP-71 proteins and wheat Skp proteins interact in vivo. Mutations in different SSGP-71 genes avoid the effector-triggered immunity that is directed by the wheat resistance genes H6 and H9. Results point to effectors as the agents responsible for arthropod-induced plant gall formation.
Nature | 2015
Oleg Simakov; Takeshi Kawashima; Ferdinand Marlétaz; Jerry Jenkins; Ryo Koyanagi; Therese Mitros; Kanako Hisata; Jessen Bredeson; Eiichi Shoguchi; Fuki Gyoja; Jia-Xing Yue; Yi-Chih Chen; Robert M. Freeman; Akane Sasaki; Tomoe Hikosaka-Katayama; Atsuko Sato; Manabu Fujie; Kenneth W. Baughman; Judith Levine; Paul Gonzalez; Christopher B. Cameron; Jens H. Fritzenwanker; Ariel M. Pani; Hiroki Goto; Miyuki Kanda; Nana Arakaki; Shinichi Yamasaki; Jiaxin Qu; Andrew Cree; Yan Ding
Acorn worms, also known as enteropneust (literally, ‘gut-breathing’) hemichordates, are marine invertebrates that share features with echinoderms and chordates. Together, these three phyla comprise the deuterostomes. Here we report the draft genome sequences of two acorn worms, Saccoglossus kowalevskii and Ptychodera flava. By comparing them with diverse bilaterian genomes, we identify shared traits that were probably inherited from the last common deuterostome ancestor, and then explore evolutionary trajectories leading from this ancestor to hemichordates, echinoderms and chordates. The hemichordate genomes exhibit extensive conserved synteny with amphioxus and other bilaterians, and deeply conserved non-coding sequences that are candidates for conserved gene-regulatory elements. Notably, hemichordates possess a deuterostome-specific genomic cluster of four ordered transcription factor genes, the expression of which is associated with the development of pharyngeal ‘gill’ slits, the foremost morphological innovation of early deuterostomes, and is probably central to their filter-feeding lifestyle. Comparative analysis reveals numerous deuterostome-specific gene novelties, including genes found in deuterostomes and marine microbes, but not other animals. The putative functions of these genes can be linked to physiological, metabolic and developmental specializations of the filter-feeding ancestor.
Genome Research | 2014
Zhen Xia Chen; David Sturgill; Jiaxin Qu; Huaiyang Jiang; Soo Park; Nathan Boley; Ana Maria Suzuki; Anthony R. Fletcher; David C. Plachetzki; Peter C. FitzGerald; Carlo G. Artieri; Joel Atallah; Olga Barmina; James B. Brown; Kerstin P. Blankenburg; Emily Clough; Abhijit Dasgupta; Sai Gubbala; Yi Han; Joy Jayaseelan; Divya Kalra; Yoo-Ah Kim; Christie Kovar; Sandra L. Lee; Mingmei Li; James D. Malley; John H. Malone; Tittu Mathew; Nicolas R Mattiuzzo; Mala Munidasa
Accurate gene model annotation of reference genomes is critical for making them useful. The modENCODE project has improved the D. melanogaster genome annotation by using deep and diverse high-throughput data. Since transcriptional activity that has been evolutionarily conserved is likely to have an advantageous function, we have performed large-scale interspecific comparisons to increase confidence in predicted annotations. To support comparative genomics, we filled in divergence gaps in the Drosophila phylogeny by generating draft genomes for eight new species. For comparative transcriptome analysis, we generated mRNA expression profiles on 81 samples from multiple tissues and developmental stages of 15 Drosophila species, and we performed cap analysis of gene expression in D. melanogaster and D. pseudoobscura. We also describe conservation of four distinct core promoter structures composed of combinations of elements at three positions. Overall, each type of genomic feature shows a characteristic divergence rate relative to neutral models, highlighting the value of multispecies alignment in annotating a target genome that should prove useful in the annotation of other high priority genomes, especially human and other mammalian genomes that are rich in noncoding sequences. We report that the vast majority of elements in the annotation are evolutionarily conserved, indicating that the annotation will be an important springboard for functional genetic testing by the Drosophila community.
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 (650u2009Mb) 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.
BMC Biology | 2017
Evelyn E. Schwager; Prashant P. Sharma; Thomas H. Clarke; Daniel J. Leite; Torsten Wierschin; Matthias Pechmann; Yasuko Akiyama-Oda; Lauren Esposito; Jesper Bechsgaard; Trine Bilde; Alexandra D. Buffry; Hsu Chao; Huyen Dinh; HarshaVardhan Doddapaneni; Shannon Dugan; Cornelius Eibner; Cassandra G. Extavour; Peter Funch; Jessica E. Garb; Luis B. Gonzalez; Vanessa L. González; Sam Griffiths-Jones; Yi Han; Cheryl Y. Hayashi; Maarten Hilbrant; Daniel S.T. Hughes; Ralf Janssen; Sandra L. Lee; Ignacio Maeso; Shwetha C. Murali
BackgroundThe duplication of genes can occur through various mechanisms and is thought to make a major contribution to the evolutionary diversification of organisms. There is increasing evidence for a large-scale duplication of genes in some chelicerate lineages including two rounds of whole genome duplication (WGD) in horseshoe crabs. To investigate this further, we sequenced and analyzed the genome of the common house spider Parasteatoda tepidariorum.ResultsWe found pervasive duplication of both coding and non-coding genes in this spider, including two clusters of Hox genes. Analysis of synteny conservation across the P. tepidariorum genome suggests that there has been an ancient WGD in spiders. Comparison with the genomes of other chelicerates, including that of the newly sequenced bark scorpion Centruroides sculpturatus, suggests that this event occurred in the common ancestor of spiders and scorpions, and is probably independent of the WGDs in horseshoe crabs. Furthermore, characterization of the sequence and expression of the Hox paralogs in P. tepidariorum suggests that many have been subject to neo-functionalization and/or sub-functionalization since their duplication.ConclusionsOur results reveal that spiders and scorpions are likely the descendants of a polyploid ancestor that lived more than 450 MYA. Given the extensive morphological diversity and ecological adaptations found among these animals, rivaling those of vertebrates, our study of the ancient WGD event in Arachnopulmonata provides a new comparative platform to explore common and divergent evolutionary outcomes of polyploidization events across eukaryotes.
Genome Biology | 2016
Alexie Papanicolaou; Marc F. Schetelig; Peter Arensburger; Peter W. Atkinson; Joshua B. Benoit; Kostas Bourtzis; Pedro Castañera; John P. Cavanaugh; Hsu Chao; Christopher Childers; Ingrid Curril; Huyen Dinh; HarshaVardhan Doddapaneni; Amanda Dolan; Shannon Dugan; Markus Friedrich; Giuliano Gasperi; Scott M. Geib; Georgios Georgakilas; Richard A. Gibbs; Sarah D. Giers; Ludvik M. Gomulski; Miguel González-Guzmán; Ana Guillem-Amat; Yi Han; Artemis G. Hatzigeorgiou; Pedro Hernández-Crespo; Daniel S.T. Hughes; Jeffery W. Jones; Dimitra Karagkouni
The Mediterranean fruit fly (medfly), Ceratitis capitata, is a major destructive insect pest due to its broad host range, which includes hundreds of fruits and vegetables. It exhibits a unique ability to invade and adapt to ecological niches throughout tropical and subtropical regions of the world, though medfly infestations have been prevented and controlled by the sterile insect technique (SIT) as part of integrated pest management programs (IPMs). The genetic analysis and manipulation of medfly has been subject to intensive study in an effort to improve SIT efficacy and other aspects of IPM control. The 479 Mb medfly genome is sequenced from adult flies from lines inbred for 20 generations. A high-quality assembly is achieved having a contig N50 of 45.7 kb and scaffold N50 of 4.06 Mb. In-depth curation of more than 1800 messenger RNAs shows specific gene expansions that can be related to invasiveness and host adaptation, including gene families for chemoreception, toxin and insecticide metabolism, cuticle proteins, opsins, and aquaporins. We identify genes relevant to IPM control, including those required to improve SIT. The medfly genome sequence provides critical insights into the biology of one of the most serious and widespread agricultural pests. This knowledge should significantly advance the means of controlling the size and invasive potential of medfly populations. Its close relationship to Drosophila, and other insect species important to agriculture and human health, will further comparative functional and structural studies of insect genomes that should broaden our understanding of gene family evolution.