Andrew R. Reynolds
Institute of Cancer Research
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Publication
Featured researches published by Andrew R. Reynolds.
Nature Communications | 2011
Keyan Zhao; Chih-Wei Tung; Georgia C. Eizenga; Mark H. Wright; M. Liakat Ali; Adam H. Price; Gareth J. Norton; S. M. Rafiqul Islam; Andrew R. Reynolds; Jason G. Mezey; Anna M. McClung; Carlos Bustamante; Susan R. McCouch
Asian rice, Oryza sativa is a cultivated, inbreeding species that feeds over half of the worlds population. Understanding the genetic basis of diverse physiological, developmental, and morphological traits provides the basis for improving yield, quality and sustainability of rice. Here we show the results of a genome-wide association study based on genotyping 44,100 SNP variants across 413 diverse accessions of O. sativa collected from 82 countries that were systematically phenotyped for 34 traits. Using cross-population-based mapping strategies, we identified dozens of common variants influencing numerous complex traits. Significant heterogeneity was observed in the genetic architecture associated with subpopulation structure and response to environment. This work establishes an open-source translational research platform for genome-wide association studies in rice that directly links molecular variation in genes and metabolic pathways with the germplasm resources needed to accelerate varietal development and crop improvement.
Nature | 2010
Bridgett M. vonHoldt; John P. Pollinger; Kirk E. Lohmueller; Eunjung Han; Heidi G. Parker; Pascale Quignon; Jeremiah D. Degenhardt; Adam R. Boyko; Dent Earl; Adam Auton; Andrew R. Reynolds; Kasia Bryc; Abra Brisbin; James C. Knowles; Dana S. Mosher; Tyrone C. Spady; Abdel G. Elkahloun; Eli Geffen; Malgorzata Pilot; Włodzimierz Jędrzejewski; Claudia Greco; Ettore Randi; Danika L. Bannasch; Alan N. Wilton; Jeremy Shearman; Marco Musiani; Michelle Cargill; Paul Glyn Jones; Zuwei Qian; Wei Huang
Advances in genome technology have facilitated a new understanding of the historical and genetic processes crucial to rapid phenotypic evolution under domestication. To understand the process of dog diversification better, we conducted an extensive genome-wide survey of more than 48,000 single nucleotide polymorphisms in dogs and their wild progenitor, the grey wolf. Here we show that dog breeds share a higher proportion of multi-locus haplotypes unique to grey wolves from the Middle East, indicating that they are a dominant source of genetic diversity for dogs rather than wolves from east Asia, as suggested by mitochondrial DNA sequence data. Furthermore, we find a surprising correspondence between genetic and phenotypic/functional breed groupings but there are exceptions that suggest phenotypic diversification depended in part on the repeated crossing of individuals with novel phenotypes. Our results show that Middle Eastern wolves were a critical source of genome diversity, although interbreeding with local wolf populations clearly occurred elsewhere in the early history of specific lineages. More recently, the evolution of modern dog breeds seems to have been an iterative process that drew on a limited genetic toolkit to create remarkable phenotypic diversity.
Nature Medicine | 2009
Andrew R. Reynolds; Ian R. Hart; Alan Watson; Jonathan C. Welti; Rita Silva; Stephen Robinson; Georges Da Violante; Morgane Gourlaouen; Mishal Salih; Matt C Jones; Dylan T. Jones; Garry Saunders; Vassiliki Kostourou; Françoise Perron-Sierra; Jim C. Norman; Gordon C Tucker; Kairbaan Hodivala-Dilke
Inhibitors of αvβ3 and αvβ5 integrin have entered clinical trials as antiangiogenic agents for cancer treatment but generally have been unsuccessful. Here we present in vivo evidence that low (nanomolar) concentrations of RGD-mimetic αvβ3 and αvβ5 inhibitors can paradoxically stimulate tumor growth and tumor angiogenesis. We show that low concentrations of these inhibitors promote VEGF-mediated angiogenesis by altering αvβ3 integrin and vascular endothelial growth factor receptor-2 trafficking, thereby promoting endothelial cell migration to VEGF. The proangiogenic effects of low concentrations of RGD-mimetic integrin inhibitors could compromise their efficacy as anticancer agents and have major implications for the use of RGD-mimetic compounds in humans.
Proceedings of the National Academy of Sciences of the United States of America | 2011
Sean Myles; Adam R. Boyko; Christopher Owens; Patrick J. Brown; F. Grassi; Mallikarjuna K. Aradhya; Bernard Prins; Andrew R. Reynolds; Jer-Ming Chia; Doreen Ware; Carlos Bustamante; Edward S. Buckler
The grape is one of the earliest domesticated fruit crops and, since antiquity, it has been widely cultivated and prized for its fruit and wine. Here, we characterize genome-wide patterns of genetic variation in over 1,000 samples of the domesticated grape, Vitis vinifera subsp. vinifera, and its wild relative, V. vinifera subsp. sylvestris from the US Department of Agriculture grape germplasm collection. We find support for a Near East origin of vinifera and present evidence of introgression from local sylvestris as the grape moved into Europe. High levels of genetic diversity and rapid linkage disequilibrium (LD) decay have been maintained in vinifera, which is consistent with a weak domestication bottleneck followed by thousands of years of widespread vegetative propagation. The considerable genetic diversity within vinifera, however, is contained within a complex network of close pedigree relationships that has been generated by crosses among elite cultivars. We show that first-degree relationships are rare between wine and table grapes and among grapes from geographically distant regions. Our results suggest that although substantial genetic diversity has been maintained in the grape subsequent to domestication, there has been a limited exploration of this diversity. We propose that the adoption of vegetative propagation was a double-edged sword: Although it provided a benefit by ensuring true breeding cultivars, it also discouraged the generation of unique cultivars through crosses. The grape currently faces severe pathogen pressures, and the long-term sustainability of the grape and wine industries will rely on the exploitation of the grapes tremendous natural genetic diversity.
Angiogenesis | 2014
Naveen S. Vasudev; Andrew R. Reynolds
Abstract Tumours require a vascular supply to grow and can achieve this via the expression of pro-angiogenic growth factors, including members of the vascular endothelial growth factor (VEGF) family of ligands. Since one or more of the VEGF ligand family is overexpressed in most solid cancers, there was great optimism that inhibition of the VEGF pathway would represent an effective anti-angiogenic therapy for most tumour types. Encouragingly, VEGF pathway targeted drugs such as bevacizumab, sunitinib and aflibercept have shown activity in certain settings. However, inhibition of VEGF signalling is not effective in all cancers, prompting the need to further understand how the vasculature can be effectively targeted in tumours. Here we present a succinct review of the progress with VEGF-targeted therapy and the unresolved questions that exist in the field: including its use in different disease stages (metastatic, adjuvant, neoadjuvant), interactions with chemotherapy, duration and scheduling of therapy, potential predictive biomarkers and proposed mechanisms of resistance, including paradoxical effects such as enhanced tumour aggressiveness. In terms of future directions, we discuss the need to delineate further the complexities of tumour vascularisation if we are to develop more effective and personalised anti-angiogenic therapies.
PLOS Biology | 2010
Adam R. Boyko; Pascale Quignon; Lin Li; Jeffrey J. Schoenebeck; Jeremiah D. Degenhardt; Kirk E. Lohmueller; Keyan Zhao; Abra Brisbin; Heidi G. Parker; Bridgett M. vonHoldt; Michele Cargill; Adam Auton; Andrew R. Reynolds; Abdel G. Elkahloun; Marta Castelhano; Dana S. Mosher; Nathan B. Sutter; Gary S. Johnson; John Novembre; Melissa J. Hubisz; Adam Siepel; Robert K. Wayne; Carlos Bustamante; Elaine A. Ostrander
The largest genetic study to date of morphology in domestic dogs identifies genes controlling nearly 100 morphological traits and identifies important trends in phenotypic variation within this species.
Proceedings of the National Academy of Sciences of the United States of America | 2010
Katarzyna Bryc; Christopher Velez; Tatiana M. Karafet; Andres Moreno-Estrada; Andrew R. Reynolds; Adam Auton; Michael F. Hammer; Carlos Bustamante; Harry Ostrer
Hispanic/Latino populations possess a complex genetic structure that reflects recent admixture among and potentially ancient substructure within Native American, European, and West African source populations. Here, we quantify genome-wide patterns of SNP and haplotype variation among 100 individuals with ancestry from Ecuador, Colombia, Puerto Rico, and the Dominican Republic genotyped on the Illumina 610-Quad arrays and 112 Mexicans genotyped on Affymetrix 500K platform. Intersecting these data with previously collected high-density SNP data from 4,305 individuals, we use principal component analysis and clustering methods FRAPPE and STRUCTURE to investigate genome-wide patterns of African, European, and Native American population structure within and among Hispanic/Latino populations. Comparing autosomal, X and Y chromosome, and mtDNA variation, we find evidence of a significant sex bias in admixture proportions consistent with disproportionate contribution of European male and Native American female ancestry to present-day populations. We also find that patterns of linkage-disequilibria in admixed Hispanic/Latino populations are largely affected by the admixture dynamics of the populations, with faster decay of LD in populations of higher African ancestry. Finally, using the locus-specific ancestry inference method LAMP, we reconstruct fine-scale chromosomal patterns of admixture. We document moderate power to differentiate among potential subcontinental source populations within the Native American, European, and African segments of the admixed Hispanic/Latino genomes. Our results suggest future genome-wide association scans in Hispanic/Latino populations may require correction for local genomic ancestry at a subcontinental scale when associating differences in the genome with disease risk, progression, and drug efficacy, as well as for admixture mapping.
Proceedings of the National Academy of Sciences of the United States of America | 2011
Jeanmaire Molina; Martin Sikora; Nandita R. Garud; Jonathan M. Flowers; Samara Rubinstein; Andrew R. Reynolds; Pu Huang; Scott A. Jackson; Barbara A. Schaal; Carlos Bustamante; Adam R. Boyko; Michael D. Purugganan
Asian rice, Oryza sativa, is one of worlds oldest and most important crop species. Rice is believed to have been domesticated ∼9,000 y ago, although debate on its origin remains contentious. A single-origin model suggests that two main subspecies of Asian rice, indica and japonica, were domesticated from the wild rice O. rufipogon. In contrast, the multiple independent domestication model proposes that these two major rice types were domesticated separately and in different parts of the species range of wild rice. This latter view has gained much support from the observation of strong genetic differentiation between indica and japonica as well as several phylogenetic studies of rice domestication. We reexamine the evolutionary history of domesticated rice by resequencing 630 gene fragments on chromosomes 8, 10, and 12 from a diverse set of wild and domesticated rice accessions. Using patterns of SNPs, we identify 20 putative selective sweeps on these chromosomes in cultivated rice. Demographic modeling based on these SNP data and a diffusion-based approach provide the strongest support for a single domestication origin of rice. Bayesian phylogenetic analyses implementing the multispecies coalescent and using previously published phylogenetic sequence datasets also point to a single origin of Asian domesticated rice. Finally, we date the origin of domestication at ∼8,200–13,500 y ago, depending on the molecular clock estimate that is used, which is consistent with known archaeological data that suggests rice was first cultivated at around this time in the Yangtze Valley of China.
Arteriosclerosis, Thrombosis, and Vascular Biology | 2007
Laura Piqueras; Andrew R. Reynolds; Kairbaan Hodivala-Dilke; Arantzazu Alfranca; Juan Miguel Redondo; Toshihisa Hatae; Tadashi Tanabe; Timothy D. Warner; David Bishop-Bailey
Objective—The role of the nuclear receptor peroxisome-proliferator activated receptor (PPAR)-&bgr;/&dgr; in endothelial cells remains unclear. Interestingly, the selective PPAR&bgr;/&dgr; ligand GW501516 is in phase II clinical trials for dyslipidemia. Here, using GW501516, we have assessed the involvement of PPAR&bgr;/&dgr; in endothelial cell proliferation and angiogenesis. Methods and Results—Western blot analysis indicated PPAR&bgr;/&dgr; was expressed in primary human umbilical and aortic endothelial cells, and in the endothelial cell line, EAHy926. Treatment with GW501516 increased human endothelial cell proliferation and morphogenesis in cultures in vitro, endothelial cell outgrowth from murine aortic vessels in vitro, and angiogenesis in a murine matrigel plug assay in vivo. GW501516 induced vascular endothelial cell growth factor mRNA and peptide release, as well as adipose differentiation-related protein (ADRP), a PPAR&bgr;/&dgr; target gene. GW501516-induced proliferation, morphogenesis, vascular endothelial growth factor (VEGF), and ADRP were absent in endothelial cells transfected with dominant-negative PPAR&bgr;/&dgr;. Furthermore, treatment of cells with cyclo-VEGFI, a VEGF receptor1/2 antagonist, abolished GW501516-induced endothelial cell proliferation and tube formation. Conclusions—PPAR&bgr;/&dgr; is a novel regulator of endothelial cell proliferation and angiogenesis through VEGF. The use of GW501516 to treat dyslipidemia may need to be carefully monitored in patients susceptible to angiogenic disorders.
PLOS ONE | 2010
Keyan Zhao; Mark G. Wright; Jennifer A. Kimball; Georgia C. Eizenga; Anna M. McClung; Michael J. Kovach; Wricha Tyagi; Md. Liakat Ali; Chih-Wei Tung; Andrew R. Reynolds; Carlos Bustamante; Susan R. McCouch
Background The domestication of Asian rice (Oryza sativa) was a complex process punctuated by episodes of introgressive hybridization among and between subpopulations. Deep genetic divergence between the two main varietal groups (Indica and Japonica) suggests domestication from at least two distinct wild populations. However, genetic uniformity surrounding key domestication genes across divergent subpopulations suggests cultural exchange of genetic material among ancient farmers. Methodology/Principal Findings In this study, we utilize a novel 1,536 SNP panel genotyped across 395 diverse accessions of O. sativa to study genome-wide patterns of polymorphism, to characterize population structure, and to infer the introgression history of domesticated Asian rice. Our population structure analyses support the existence of five major subpopulations (indica, aus, tropical japonica, temperate japonica and GroupV) consistent with previous analyses. Our introgression analysis shows that most accessions exhibit some degree of admixture, with many individuals within a population sharing the same introgressed segment due to artificial selection. Admixture mapping and association analysis of amylose content and grain length illustrate the potential for dissecting the genetic basis of complex traits in domesticated plant populations. Conclusions/Significance Genes in these regions control a myriad of traits including plant stature, blast resistance, and amylose content. These analyses highlight the power of population genomics in agricultural systems to identify functionally important regions of the genome and to decipher the role of human-directed breeding in refashioning the genomes of a domesticated species.