Kristofer M. Helgen
University of Adelaide
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Featured researches published by Kristofer M. Helgen.
Journal of Heredity | 2009
David Haussler; Stephen J. O'Brien; Oliver A. Ryder; F. Keith Barker; Michele Clamp; Andrew J. Crawford; Robert Hanner; Olivier Hanotte; Warren E. Johnson; Jimmy A. McGuire; Webb Miller; Robert W. Murphy; William J. Murphy; Frederick H. Sheldon; Barry Sinervo; Byrappa Venkatesh; E. O. Wiley; Fred W. Allendorf; George Amato; C. Scott Baker; Aaron M. Bauer; Albano Beja-Pereira; Eldredge Bermingham; Giacomo Bernardi; Cibele R. Bonvicino; Sydney Brenner; Terry Burke; Joel Cracraft; Mark Diekhans; Scott V. Edwards
The human genome project has been recently complemented by whole-genome assessment sequence of 32 mammals and 24 nonmammalian vertebrate species suitable for comparative genomic analyses. Here we anticipate a precipitous drop in costs and increase in sequencing efficiency, with concomitant development of improved annotation technology and, therefore, propose to create a collection of tissue and DNA specimens for 10,000 vertebrate species specifically designated for whole-genome sequencing in the very near future. For this purpose, we, the Genome 10K Community of Scientists (G10KCOS), will assemble and allocate a biospecimen collection of some 16,203 representative vertebrate species spanning evolutionary diversity across living mammals, birds, nonavian reptiles, amphibians, and fishes (ca. 60,000 living species). In this proposal, we present precise counts for these 16,203 individual species with specimens presently tagged and stipulated for DNA sequencing by the G10KCOS. DNA sequencing has ushered in a new era of investigation in the biological sciences, allowing us to embark for the first time on a truly comprehensive study of vertebrate evolution, the results of which will touch nearly every aspect of vertebrate biological enquiry.
Proceedings of the National Academy of Sciences of the United States of America | 2011
Webb Miller; Vanessa M. Hayes; Aakrosh Ratan; Desiree C. Petersen; Nicola E. Wittekindt; Jason R. Miller; Brian Walenz; James Knight; Ji Qi; Fangqing Zhao; Qingyu Wang; Oscar C. Bedoya-Reina; Neerja Katiyar; Lynn P. Tomsho; Lindsay McClellan Kasson; Rae-Anne Hardie; Paula Woodbridge; Elizabeth A. Tindall; Mads F. Bertelsen; Dale Dixon; Stephen Pyecroft; Kristofer M. Helgen; Arthur M. Lesk; Thomas H. Pringle; Nick Patterson; Yu Zhang; Alexandre Kreiss; Gm Woods; Menna E. Jones; Stephan C. Schuster
The Tasmanian devil (Sarcophilus harrisii) is threatened with extinction because of a contagious cancer known as Devil Facial Tumor Disease. The inability to mount an immune response and to reject these tumors might be caused by a lack of genetic diversity within a dwindling population. Here we report a whole-genome analysis of two animals originating from extreme northwest and southeast Tasmania, the maximal geographic spread, together with the genome from a tumor taken from one of them. A 3.3-Gb de novo assembly of the sequence data from two complementary next-generation sequencing platforms was used to identify 1 million polymorphic genomic positions, roughly one-quarter of the number observed between two genetically distant human genomes. Analysis of 14 complete mitochondrial genomes from current and museum specimens, as well as mitochondrial and nuclear SNP markers in 175 animals, suggests that the observed low genetic diversity in todays population preceded the Devil Facial Tumor Disease disease outbreak by at least 100 y. Using a genetically characterized breeding stock based on the genome sequence will enable preservation of the extant genetic diversity in future Tasmanian devil populations.
Journal of Mammalogy | 2009
Kristofer M. Helgen; F. Russell Cole; Lauren E. Helgen; Don E. Wilson
Abstract The substantial body of research on Holarctic ground squirrels amassed over the past century documents considerable variability in morphological, cytogenetic, ecological, and behavioral attributes in the genus Spermophilus F. Cuvier, 1825. Recent molecular phylogenetic studies suggest that the traditionally recognized genera Marmota Blumenbach, 1779 (marmots), Cynomys Rafinesque, 1817 (prairie dogs), and Ammospermophilus Merriam, 1892 (antelope ground squirrels) render Spermophilus paraphyletic, potentially suggesting that multiple generic-level lineages should be credited within Spermophilus. Herein, we recognize 8 genera formerly subsumed in Spermophilus, each of which is morphologically diagnosable, craniometrically distinctive, and recovered as a monophyletic clade in phylogenetic analyses utilizing the mitochondrial gene cytochrome b. Generic-level names are available for each of these ground squirrel assemblages, most of which are exclusively or predominantly North American in distribution (Notocitellus A. H. Howell, 1938; Otospermophilus Brandt, 1844; Callospermophilus Merriam, 1897; Ictidomys J. A. Allen, 1877; Poliocitellus A. H. Howell, 1938; Xerospermophilus Merriam, 1892; and Urocitellus Obolenskij, 1927). Only Spermophilus sensu stricto is restricted to Eurasia. Generic subdivision of Spermophilus more aptly illuminates the taxonomic relationships, ecomorphological disparity, and biogeographic history of Holarctic ground squirrels.
Nature | 2004
Alfred L. Roca; Gila Kahila Bar-Gal; Eduardo Eizirik; Kristofer M. Helgen; Roberto María; Mark S. Springer; Stephen J. O'Brien; William J. Murphy
The highly endangered solenodons, endemic to Cuba (Solenodon cubanus) and Hispaniola (S. paradoxus), comprise the only two surviving species of West Indian insectivores. Combined gene sequences (13.9 kilobases) from S. paradoxus established that solenodons diverged from other eulipotyphlan insectivores 76 million years ago in the Cretaceous period, which is consistent with vicariance, though also compatible with dispersal. A sequence of 1.6 kilobases of mitochondrial DNA from S. cubanus indicated a deep divergence of 25 million years versus the congeneric S. paradoxus, which is consistent with vicariant origins as tectonic forces separated Cuba and Hispaniola. Efforts to prevent extinction of the two surviving solenodon species would conserve an entire lineage as old or older than many mammalian orders.
Genome Research | 2011
Victor C. Mason; Gang Li; Kristofer M. Helgen; William J. Murphy
The ability to uncover the phylogenetic history of recently extinct species and other species known only from archived museum material has rapidly improved due to the reduced cost and increased sequence capacity of next-generation sequencing technologies. One limitation of these approaches is the difficulty of isolating and sequencing large, orthologous DNA regions across multiple divergent species, which is exacerbated for museum specimens, where DNA quality varies greatly between samples and contamination levels are often high. Here we describe the use of cross-species DNA capture hybridization techniques and next-generation sequencing to selectively isolate and sequence partial to full-length mitochondrial DNA genomes from the degraded DNA of museum specimens, using probes generated from the DNA of a single extant species. We demonstrate our approach on specimens from an enigmatic gliding mammal, the Sunda colugo, which is widely distributed throughout Southeast Asia. We isolated DNA from 13 colugo specimens collected 47-170 years ago, and successfully captured and sequenced mitochondrial DNA from every specimen, frequently recovering fragments with 10%-13% sequence divergence from the capture probe sequence. Phylogenetic results reveal deep genetic divergence among colugos, both within and between the islands of Borneo and Java, as well as between the Malay Peninsula and different Sundaic islands. Our method is based on noninvasive sampling of minute amounts of soft tissue material from museum specimens, leaving the original specimen essentially undamaged. This approach represents a paradigm shift away from standard PCR-based approaches for accessing population genetic and phylogenomic information from poorly known and difficult-to-study species.
BMC Evolutionary Biology | 2010
Robert J. Asher; Kristofer M. Helgen
An issue arising from recent progress in establishing the placental mammal Tree of Life concerns the nomenclature of high-level clades. Fortunately, there are now several well-supported clades among extant mammals that require unambiguous, stable names. Although the International Code of Zoological Nomenclature does not apply above the Linnean rank of family, and while consensus on the adoption of competing systems of nomenclature does not yet exist, there is a clear, historical basis upon which to arbitrate among competing names for high-level mammalian clades. Here, we recommend application of the principles of priority and stability, as laid down by G.G. Simpson in 1945, to discriminate among proposed names for high-level taxa. We apply these principles to specific cases among placental mammals with broad relevance for taxonomy, and close with particular emphasis on the Afrotherian family Tenrecidae. We conclude that no matter how reconstructions of the Tree of Life change in years to come, systematists should apply new names reluctantly, deferring to those already published and maximizing consistency with existing nomenclature.
PLOS ONE | 2013
Julia T. Vilstrup; Andaine Seguin-Orlando; Mathias Stiller; Aurélien Ginolhac; Maanasa Raghavan; Sandra C. Abel Nielsen; Jacobo Weinstock; Duane G. Froese; Sergei K. Vasiliev; Nikolai D. Ovodov; Joel Clary; Kristofer M. Helgen; Robert C. Fleischer; Alan Cooper; Beth Shapiro; Ludovic Orlando
The genus Equus is richly represented in the fossil record, yet our understanding of taxonomic relationships within this genus remains limited. To estimate the phylogenetic relationships among modern horses, zebras, asses and donkeys, we generated the first data set including complete mitochondrial sequences from all seven extant lineages within the genus Equus. Bayesian and Maximum Likelihood phylogenetic inference confirms that zebras are monophyletic within the genus, and the Plains and Grevy’s zebras form a well-supported monophyletic group. Using ancient DNA techniques, we further characterize the complete mitochondrial genomes of three extinct equid lineages (the New World stilt-legged horses, NWSLH; the subgenus Sussemionus; and the Quagga, Equus quagga quagga). Comparisons with extant taxa confirm the NWSLH as being part of the caballines, and the Quagga and Plains zebras as being conspecific. However, the evolutionary relationships among the non-caballine lineages, including the now-extinct subgenus Sussemionus, remain unresolved, most likely due to extremely rapid radiation within this group. The closest living outgroups (rhinos and tapirs) were found to be too phylogenetically distant to calibrate reliable molecular clocks. Additional mitochondrial genome sequence data, including radiocarbon dated ancient equids, will be required before revisiting the exact timing of the lineage radiation leading up to modern equids, which for now were found to have possibly shared a common ancestor as far as up to 4 Million years ago (Mya).
Journal of Ecology | 2013
Hillary S. Young; Douglas J. McCauley; Kristofer M. Helgen; Jacob R. Goheen; Erik Otárola-Castillo; Todd M. Palmer; Robert M. Pringle; Truman P. Young; Rodolfo Dirzo
1. Herbivores influence the structure and composition of terrestrial plant communities. However, responses of plant communities to herbivory are variable and depend on environmental conditions, herbivore identity and herbivore abundance. As anthropogenic impacts continue to drive large declines in wild herbivores, understanding the context dependence of herbivore impacts on plant communities becomes increasingly important. 2. Exclosure experiments are frequently used to assess how ecosystems reorganize in the face of large wild herbivore defaunation. Yet in many landscapes, declines in large wildlife are often accompanied by other anthropogenic activities, especially land conversion to livestock production. In such cases, exclosure experiments may not reflect typical outcomes of human-driven extirpations of wild herbivores. 3. Here, we examine how plant community responses to changes in the identity and abundance of large herbivores interact with abiotic factors (rainfall and soil properties). We also explore how effects of wild herbivores on plant communities differ between large-scale herbivore exclosures and landscape sites where anthropogenic activity has caused wildlife declines, often accompanied by livestock increases. 4. Abiotic context modulated the responses of plant communities to herbivore declines with stronger effect sizes in lower-productivity environments. Also, shifts in plant community structure, composition and species richness following wildlife declines differed considerably between exclosure experiments and landscape sites in which wild herbivores had declined and were often replaced by livestock. Plant communities in low wildlife landscape sites were distinct in both composition and physical structure from both exclosure and control sites in experiments. The power of environmental (soil and rainfall) gradients in influencing plant response to herbivores was also greatly dampened or absent in the landscape sites. One likely explanation for these observed differences is the compensatory effect of livestock associated with the depression or extirpation of wildlife. 5. Synthesis. Our results emphasize the importance of abiotic environmental heterogeneity in modulating the effects of mammalian herbivory on plant communities and the importance of such covariation in understanding effects of wild herbivore declines. They also suggest caution when extrapolating results from exclosure experiments to predict the consequences of defaunation as it proceeds in the Anthropocene.
Current Biology | 2015
Klaus-Peter Koepfli; John P. Pollinger; Raquel Godinho; Jacqueline Robinson; Amanda J. Lea; Sarah A. Hendricks; Rena M. Schweizer; Olaf Thalmann; Pedro Miguel Silva; Zhenxin Fan; Andrey A. Yurchenko; Pavel Dobrynin; Alexey I. Makunin; James A. Cahill; Beth Shapiro; Francisco Álvares; José Carlos Brito; Eli Geffen; Jennifer A. Leonard; Kristofer M. Helgen; Warren E. Johnson; Stephen J. O’Brien; Blaire Van Valkenburgh; Robert K. Wayne
The golden jackal of Africa (Canis aureus) has long been considered a conspecific of jackals distributed throughout Eurasia, with the nearest source populations in the Middle East. However, two recent reports found that mitochondrial haplotypes of some African golden jackals aligned more closely to gray wolves (Canis lupus), which is surprising given the absence of gray wolves in Africa and the phenotypic divergence between the two species. Moreover, these results imply the existence of a previously unrecognized phylogenetically distinct species despite a long history of taxonomic work on African canids. To test the distinct-species hypothesis and understand the evolutionary history that would account for this puzzling result, we analyzed extensive genomic data including mitochondrial genome sequences, sequences from 20 autosomal loci (17 introns and 3 exon segments), microsatellite loci, X- and Y-linked zinc-finger protein gene (ZFX and ZFY) sequences, and whole-genome nuclear sequences in African and Eurasian golden jackals and gray wolves. Our results provide consistent and robust evidence that populations of golden jackals from Africa and Eurasia represent distinct monophyletic lineages separated for more than one million years, sufficient to merit formal recognition as different species: C. anthus (African golden wolf) and C. aureus (Eurasian golden jackal). Using morphologic data, we demonstrate a striking morphologic similarity between East African and Eurasian golden jackals, suggesting parallelism, which may have misled taxonomists and likely reflects uniquely intense interspecific competition in the East African carnivore guild. Our study shows how ecology can confound taxonomy if interspecific competition constrains size diversification.
Molecular Biology and Evolution | 2013
María C. Ávila-Arcos; Simon Y. W. Ho; Yasuko Ishida; Nikolas Nikolaidis; Kyriakos Tsangaras; Karin Hönig; Rebeca Medina; Morten Rasmussen; Sarah L. Fordyce; Sébastien Calvignac-Spencer; M. Thomas P. Gilbert; Kristofer M. Helgen; Alfred L. Roca; Alex D. Greenwood
Although endogenous retroviruses are common across vertebrate genomes, the koala retrovirus (KoRV) is the only retrovirus known to be currently invading the germ line of its host. KoRV is believed to have first infected koalas in northern Australia less than two centuries ago. We examined KoRV in 28 koala museum skins collected in the late 19th and 20th centuries and deep sequenced the complete proviral envelope region from five northern Australian specimens. Strikingly, KoRV env sequences were conserved among koalas collected over the span of a century, and two functional motifs that affect viral infectivity were fixed across the museum koala specimens. We detected only 20 env polymorphisms among the koalas, likely representing derived mutations subject to purifying selection. Among northern Australian koalas, KoRV was already ubiquitous by the late 19th century, suggesting that KoRV evolved and spread among koala populations more slowly than previously believed. Given that museum and modern koalas share nearly identical KoRV sequences, it is likely that koala populations, for more than a century, have experienced increased susceptibility to diseases caused by viral pathogenesis.