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PHYML online—a web server for fast maximum likelihood-based phylogenetic inference. Nucleic Acids Res. (2005)

by S Guindon, F Lethiec, P Duroux, O Gascuel
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E: Conditioned genome reconstruction: how to avoid choosing the conditioning genome

by Matthew Spencer, David Bryant, Edward Susko - Syst Biol 2007
"... Abstract.—Genome phylogenies can be inferred from data on the presence and absence of genes across taxa. Logdet distances may be a good method, because they allow expected genome size to vary across the tree. Recently, Lake and Rivera proposed conditioned genome reconstruction (calculation of logdet ..."
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Abstract.—Genome phylogenies can be inferred from data on the presence and absence of genes across taxa. Logdet distances may be a good method, because they allow expected genome size to vary across the tree. Recently, Lake and Rivera proposed conditioned genome reconstruction (calculation of logdet distances using only those genes present in a conditioning genome) to deal with unobservable genes that are absent from every taxon of interest. We prove that their method can consistently estimate the topology for almost any choice of conditioning genome. Nevertheless, the choice of conditioning genome is important for small samples. For real bacterial genome data, different choices of conditioning genome can result in strong bootstrap support for different tree topologies. To overcome this problem, we developed supertree methods that combine information from all choices of conditioning genome. One of these methods, based on the BIONJ algorithm, performs well on simulated data and may have applications to other supertree problems. However, an analysis of 40 bacterial genomes using this method supports an incorrect clade of parasites. This is a common feature of model-based gene content methods and is due to parallel gene loss. [BIONJ; conditioned genome reconstruction; consistency; gene content; logdet; supertrees.] Variation in gene content makes it difficult to estimate organismal phylogeny from nucleotide or amino acid se-quences. Within a lineage, genes are often gained (for example, by lateral transfer) and lost (by deletion). Both
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... real. We estimated the maximum likelihood tree topology for 16s rRNA sequences (from the Ribosomal Database Project II, release 9, http://rdp.cme.msu.edu/, downloaded 3 May 2006) using PHYML Online (=-=Guindon et al., 2005-=-, http://atgc.lirmm.fr/phyml/, accessed 18 May 2006) with discrete gamma rate variation, four gamma categories, and a general time-reversible model. There is little correlation between the edge length...

Plastid-derived genes in the nonphotosynthetic alveolate Oxyrrhis marina. Mol Biol Evol

by Claudio H Slamovits , Patrick J Keeling , 2008
"... Reconstructing the history of plastid acquisition and loss in the alveolate protists is a difficult problem because our knowledge of the distribution of plastids in extant lineages is incomplete due to the possible presence of cryptic, nonphotosynthetic plastids in several lineages. The discovery o ..."
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Reconstructing the history of plastid acquisition and loss in the alveolate protists is a difficult problem because our knowledge of the distribution of plastids in extant lineages is incomplete due to the possible presence of cryptic, nonphotosynthetic plastids in several lineages. The discovery of the apicoplast in apicomplexan parasites has drawn attention to this problem and, more specifically, to the question of whether many other nonphotosynthetic lineages also contain cryptic plastids or are derived from plastid-containing ancestors. Oxyrrhis marina is one such organism: It is a heterotrophic, early-branching member of the dinoflagellate lineage for which there is no evidence of a plastid. To investigate the possibility that O. marina is derived from a photosynthetic ancestor, we have generated and analyzed a large-scale EST database and searched for evidence of plastid-derived genes. Here, we describe 8 genes whose phylogeny shows them to be derived from plastid-targeted homologues. These genes encode proteins from several pathways known to be localized in the plastids of other algae, including synthesis of tetrapyrroles, isoprenoids, and amino acids, as well as carbon metabolism and oxygen detoxification. The 5# end of 5 cDNAs were also characterized using cap-dependent or spliced leader-mediated reverse transcriptase-polymerase chain reaction, revealing that at least 4 of these genes have retained leaders that are similar in nature to the plastid-targeting signals of other secondary plastids, suggesting that these proteins may be targeted to a cryptic organelle. At least 2 genes do not encode such leaders, and their products may presently function in the cytosol. Altogether, the presence of plastid-derived genes in O. marina shows that its ancestors contained a plastid, and the pathways represented by the genes and presence of targeting signals on at least some of the genes further suggests that a relict organelle may still exist to fulfill plastid metabolic functions.
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...mbination with a forward primer based on the sequence of the spliced leader described in (Zhang et al. 2007). New sequences were deposited in GenBank under accession numbers EU551745–EU551753. Phylogenetic Analyses Candidate O. marina genes with plastid ancestry were subject to phylogenetic analyses with a wide variety of homologues. Phylogenies were initially screened using a rapid Neighbor-Joining (NJ) analysis implemented in PAUP 4.0b10 (Swofford 2002). In cases where this did not exclude the possibility of a plastid origin, phylogenies were inferred by maximum likelihood (ML) using PhyML (Guindon et al. 2005) and Bayesian analysis usingMrBayes 3 (Ronquist and Huelsenbeck 2003). For ML, a WAG model of amino acid substitution was used with 8 categories of rate variation under a gamma distribution plus invariable sites. Bootstrap support was tested with 300 replicates under the same conditions. For Bayesian analyses, a gamma correction with 8 categories and proportion of invariable sites was used, and 4 Monte Carlo Markov chains were also used (default temperature 5 0.2). In each case, a total of 1,000,000 generations was calculated with trees sampled every 100 generations and with burn-in of 200,000...

The Hotdog Thioesterase EntH (YbdB) Plays a Role In Vivo in

by The Hotdog Thioesterase Enth (ybdb, Damien Leduc, Aurélia Battesti, Emmanuelle Bouveret , 2007
"... This article cites 41 articles, 19 of which can be accessed free ..."
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This article cites 41 articles, 19 of which can be accessed free
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... proteins from other organisms were used to add structural information. The corresponding unrooted tree was constructed by a maximum likelihood method using PHYLM with the Jones-Taylor-Thornton model =-=(14)-=-. Drawing was realized using the Treeview program (30). Bootstrap values were computed by PHYLM for 100 replicates of the original data set. RESULTS YbdB protein is produced under iron limitation cond...

HIV-1 replication in the central nervous system occurs in two distinct cell types.

by G Schnell , S Joseph , S Spudich , R W Price , R Swanstrom - PLOS Pathogens 7:e1002286. , 2011
"... Abstract Human immunodeficiency virus type 1 (HIV-1) infection of the central nervous system (CNS) can lead to the development of HIV-1-associated dementia (HAD). We examined the virological characteristics of HIV-1 in the cerebrospinal fluid (CSF) of HAD subjects to explore the association between ..."
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Abstract Human immunodeficiency virus type 1 (HIV-1) infection of the central nervous system (CNS) can lead to the development of HIV-1-associated dementia (HAD). We examined the virological characteristics of HIV-1 in the cerebrospinal fluid (CSF) of HAD subjects to explore the association between independent viral replication in the CNS and the development of overt dementia. We found that genetically compartmentalized CCR5-tropic (R5) T cell-tropic and macrophage-tropic HIV-1 populations were independently detected in the CSF of subjects diagnosed with HIV-1-associated dementia. Macrophagetropic HIV-1 populations were genetically diverse, representing established CNS infections, while R5 T cell-tropic HIV-1 populations were clonally amplified and associated with pleocytosis. R5 T cell-tropic viruses required high levels of surface CD4 to enter cells, and their presence was correlated with rapid decay of virus in the CSF with therapy initiation (similar to virus in the blood that is replicating in activated T cells). Macrophage-tropic viruses could enter cells with low levels of CD4, and their presence was correlated with slow decay of virus in the CSF, demonstrating a separate long-lived cell as the source of the virus. These studies demonstrate two distinct virological states inferred from the CSF virus in subjects diagnosed with HAD. Finally, macrophage-tropic viruses were largely restricted to the CNS/CSF compartment and not the blood, and in one case we were able to identify the macrophage-tropic lineage as a minor variant nearly two years before its expansion in the CNS. These results suggest that HIV-1 variants in CSF can provide information about viral replication and evolution in the CNS, events that are likely to play an important role in HIV-associated neurocognitive disorders.
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...R DN1, and B5957 UP1 and LTR DN1, were used for the first and second rounds of PCR, respectively [48]. The SGA amplicons were sequenced from the start of V1 through the ectodomain of gp41 [Hxb2 numbering of positions 6600–8000]. Phylogenetic and compartmentalization analyses Nucleotide sequences of the env genes were aligned using Clustal W [49,50] or MAFFT software [51]. Sequences from each subject were codon aligned using GeneCutter (Los Alamos HIV-1 database; http://www.hiv.lanl.gov/content/sequence/GENE_ CUTTER/cutter.html). Maximum likelihood phylogenetic trees were generated using PhyML [52] with the following parameters: HKY85 nucleotide substitution model, four substitution rate categories, estimation of the transition/transversion rate ratio, estimation of the proportion of invariant sites, and estimation of the gamma distribution parameter [53]. Compartmentalization of CSF viral populations by sequence was determined using the Slatkin-Maddison test for compartmentalization [54] by HyPhy software [55] using 10,000 permutations. Pairwise distance was calculated for HIV-1 env sequences in the CSF-compartmentalized population using MEGA 4.1 software [56,57,58]. Construction of HI...

Bromham L: Statistical tests between competing hypotheses of Hox cluster evolution

by Robert Lanfear, Lindell Bromham - Syst Biol
"... Abstract.—The Hox genes encode transcription factors that play vital roles in the anterior-posterior patterning of all bilaterian phyla studied to date. Additionally, the gain of Hox genes by duplication has been widely implicated as a driving force in the evolution of animal body plans. Because of ..."
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Abstract.—The Hox genes encode transcription factors that play vital roles in the anterior-posterior patterning of all bilaterian phyla studied to date. Additionally, the gain of Hox genes by duplication has been widely implicated as a driving force in the evolution of animal body plans. Because of this, reconstructing the evolution of the Hox cluster has been the focus of intense research interest. It has been commonly assumed that an ancestral four-gene ProtoHox cluster was duplicated early in animal evolution to give rise to the Hox and ParaHox clusters. However, this hypothesis has recently been called into question, and a number of alternative hypotheses of Hox and ParaHox gene evolution have been proposed. Here, we present the first statistical comparisons of current hypotheses of Hox and ParaHox gene evolution. We use two statistical methods that represent two different approaches to the treatment of phylogenetic uncertainty. In the first method, we estimate the maximum-likelihood tree for each hypothesis and compare these trees to one another using a parametric bootstrapping approach. In the second method, we use Bayesian phylogenetics to estimate the posterior distribution of trees, then we calculate the support for each hypothesis from this distribution. The results of both methods are largely congruent. We find that we are able to reject five out of the eight current hypotheses of Hox and ParaHox gene evolution that we consider. We conclude that the ProtoHox cluster is likely to have contained either three or four genes but that there is insufficient phylogenetic signal in the homeodomains to distinguish between these alternatives. [Bayesian; Homeobox; maximum likelihood; phylogenetics; ProtoHox; ParaHox.]
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...3) was assessed using the Goldman-Cox test (Goldman, 1993). For each Goldman-Cox test, we first estimated the ML topology for the dataset and model in question using PhyML (Guindon and Gascuel, 2003; =-=Guindon et al., 2005-=-). We then calculated both the unconstrained (i.e., model-free) and constrained (i.e., assuming a particular model) likelihoods for this topology, as well as the free parameters of the model, using PA...

The evolutionary dynamics of autonomous non-LTR retrotransposons in the lizard Anolis carolinensis shows more similarity to fish than mammals

by Peter A Novick , Holly Basta , Mark Floumanhaft , Marcella A Mcclure , Stéphane Boissinot , 2009
"... The genome of the lizard Anolis carolinensis (the green anole) is the first nonavian reptilian genome sequenced. It offers a unique opportunity to comparatively examine the evolution of amniote genomes. We analyzed the abundance and diversity of non-LTR (long terminal repeat) retrotransposons in th ..."
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The genome of the lizard Anolis carolinensis (the green anole) is the first nonavian reptilian genome sequenced. It offers a unique opportunity to comparatively examine the evolution of amniote genomes. We analyzed the abundance and diversity of non-LTR (long terminal repeat) retrotransposons in the anole using the Genome Parsing Suite. We found that the anole genome contains an extraordinary diversity of elements. We identified 46 families of elements representing five clades (L1, L2, CR1, RTE, and R4). Within most families, elements are very similar to each other suggesting that they have been inserted recently. The rarity of old elements suggests a high rate of turnover, the insertion of new elements being offset by the loss of element-containing loci. Consequently, non-LTR retrotransposons accumulate in the anole at a low rate and are found in low copy number. This pattern of diversity shows some striking similarity with the genome of teleostean fish but contrasts greatly with the low diversity and high copy number of mammalian L1 elements, suggesting a fundamental difference in the way mammals and nonmammalian vertebrates interact with their genomic parasites. The scarcity of divergent elements in anoles suggests that insertions have a deleterious effect and are eliminated by natural selection. We propose that the low abundance of non-LTR retrotransposons in the anole is related directly or indirectly to a higher rate of ectopic recombination in the anole relative to mammals.
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...tioned novel proteins. Sequence numbers correspond to those in figure 1 and can be found under the accession numbers: 1—AF086712; 2—L25662; 3—X99080; 4—AF018033; 5—M93690; 6—X51968; 7—D38414; 8—AF012049; 9—X06950; 10—M22874; 11—M14954; 12—M28878; 13—X60372; 14—U66331; 15—U88211; 16—AB005891; 17—U73800; 18— X60177; 19—U87543; 20—Z25525; 21—AF025462; 22—U58755; 23—M26915; 24—AF081114; 25—U93574; 26—X51967; 27—U13035; 28—M16558; 29—U29445; 30—M33009; 31—M62862; and 32—X17078. These sequences were then analyzed phylogenetically using the NJ andmaximum likelihood tree usingMEGA4.0 andPHYML online (Guindon et al. 2005), respectively. Results The GPS identified a total of 1,888 FL elements in the anole. Further Blast and BLAT searches of the anole genome using the sequences collected by GPS as probes failed to detect any other FL elements, although we recovered a number of truncated (TR) elements (supplementary fig. 1, Supplementary Material online). Representatives from five of the twelve clades of non-LTR retrotransposons were detected: L1, L2, CR1, RTE, and R4 (fig. 1). These clades differ greatly in copy number and diversity. Of the five clades that inhabit the genome of A. carolinensis, L1 is the least ...

ISG20L2, a novel vertebrate nucleolar exoribonuclease involved in ribosome biogenesis, in "Molecular and cellular proteomics", L1, vol. 7, n o 3

by Karine Kindbeiter
"... Proteomics analyses of human nucleoli provided molec-ular bases for an understanding of the multiple functions fulfilled by these nuclear domains. However, the biological roles of about 100 of the identified proteins are unpredict-able. The present study describes the functional charac-terization of ..."
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Proteomics analyses of human nucleoli provided molec-ular bases for an understanding of the multiple functions fulfilled by these nuclear domains. However, the biological roles of about 100 of the identified proteins are unpredict-able. The present study describes the functional charac-terization of one of these proteins, ISG20L2. We demon-strate that ISG20L2 is a 3 to 5 exoribonuclease involved in ribosome biogenesis at the level of 5.8 S rRNA matura-tion, more specifically in the processing of the 12 S pre-cursor rRNA. The use of truncated forms of ISG20L2 dem-onstrated that its N-terminal half promotes the nucleolar localization and suggested that its C-terminal half bears the exoribonuclease activity. Identification of the binding partners of ISG20L2 confirmed its involvement in the bio-genesis of the large ribosomal subunit. These results
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...than or equal to the score of the yeast Rex1 paralog. Sequences were aligned with MUSCLE (27). The phylogenetic tree was inferred from protein sequence alignments by maximum likelihood. We used Phyml =-=(28, 29)-=- under the Jones-Taylor-Thornton model of protein evolution (30) with site-tosite rate variation modeled on a discrete distribution (four categories, shape parameter , and proportion of invariable ...

Phylogeny, biogeography, and electric signal evolution of Neotropical knifefishes of the genus Gymnotus (Osteichthyes: Gymnotidae)

by Nathan R Lovejoy , Kristie Lester , William G R Crampton , Fernando P L Marques , James S Albert
"... a b s t r a c t The Neotropical knifefish genus Gymnotus is the most broadly distributed and the most diverse (34 + species) gymnotiform genus. Its wide range includes both Central and South American drainages, including the Amazon, Orinoco, and La Plata Basins. Like all gymnotiforms, Gymnotus spec ..."
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a b s t r a c t The Neotropical knifefish genus Gymnotus is the most broadly distributed and the most diverse (34 + species) gymnotiform genus. Its wide range includes both Central and South American drainages, including the Amazon, Orinoco, and La Plata Basins. Like all gymnotiforms, Gymnotus species produce weak electric fields for both navigation and communication, and these fields exhibit interspecific variation in electric waveform characteristics. Both biogeography and electric signal evolution can profitably be analyzed in a phylogenetic context. Here, we present a total evidence phylogeny for 19 Gymnotus species based on data from the mitochondrial cytochrome b and 16S genes (1558 bp), the nuclear RAG2 gene (1223 bp), and 113 morphological characters. Our phylogenetic hypothesis resolves five distinct Gymnotus lineages. In a previous morphology-based analysis, the Central American Gymnotus cylindricus lineage was hypothesized as the sister group to all other Gymnotus species. In our analysis, the G. cylindricus lineage is nested within South American species, and molecular age estimates support a relatively recent origin for the clade in Central America. Phylogenetic optimization of electric signal waveforms indicate that the ancestral state in Gymnotus is a multiphasic (4 + phases of alternating polarity) condition, and independent phase loss has occurred in multiple lineages. Gymnotus is a model group for understanding Neotropical diversification and the evolution of communication at a continental scale.
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...tion for each node (Baker and 282 N.R. Lovejoy et al. / Molecular Phylogenetics and Evolution 54 (2010) 278–290DeSalle, 1997). Finally, we explored the effect of different character weighting schemes by inferring transition/transversion ratios from the data and using step matrices to differentially weight these state changes. We also subjected the dataset to phylogenetic analyses using maximum likelihood and Bayesian methods (Guindon and Gascuel, 2003; Ronquist and Huelsenbeck, 2003). Maximum likelihood phylogenetic methods were implemented in the program PHYML 3.0 (Guindon and Gascuel, 2003; Guindon et al., 2005), under the GTR+I+G model. This model was found to be the best fit for the unpartitioned molecular dataset, according to both hierarchical likelihood ratio tests (LRT) and Akaike Information Criterion (AIC), as implemented in Modeltest v3.7 (Posada and Crandall, 1998). For the likelihood analyses, bootstrapping methods (100 replicates) were used to assess the node support (Felsenstein, 1985b). Bayesian inference was performed in MrBayes 3.1.2 (Ronquist and Huelsenbeck, 2003). The morphological data and each of the three genes were treated as separate data partitions. All partitions had indepen...

Referred to by

by Amanda L. Lewis, Jean-bernard Lubin, Shilpa Argade, Natasha Naidu, Biswa Choudhury, A L. Lewis, Jean-bernard Lubin, Shilpa Argade, Natasha Naidu, Biswa Choudhury, E. Fidelma, Natasha Naidu, Biswa Choudhury, E. Fidelma Boyd, A L. Lewis, Jean-bernard Lubin, Shilpa Argade
"... Genomic and metabolic profiling of nonulosonic acids in Vibrionaceae reveal biochemical phenotypes of allelic divergence in Vibrio vulnificus ..."
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Genomic and metabolic profiling of nonulosonic acids in Vibrionaceae reveal biochemical phenotypes of allelic divergence in Vibrio vulnificus
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...hecked for invariant and conserved regions using GENEDOC (version 2.7; National Resource for Biomedical Supercomputing (Pittsburgh, PA) (14, 33). We used neighbor joining (NJ) as implemented in MEGA4 =-=(19, 20, 54)-=-. The bootstrap values for NJ trees were obtained after 1,000 generations, and MEGA4 tree viewer was used to visualize the trees and calculate confidence values (25, 54). 16S rRNA sequences were also ...

Evolutionary analysis of mammalian genomes and associations to human disease [PhD thesis

by Jessica Janaki Vamathevan
"... I, Jessica Janaki Vamathevan, confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis. Statistical models of DNA sequence evolution for analysing protein-coding genes can be used to estimate ..."
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I, Jessica Janaki Vamathevan, confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis. Statistical models of DNA sequence evolution for analysing protein-coding genes can be used to estimate rates of molecular evolution and to detect signals of natural selection. Genes that have undergone positive selection during evolution are indicative of functional adaptations that drive species differences. Genes that underwent positive selection during the evolution of humans and four mammals used to model human diseases (mouse, rat, chimpanzee and dog) were identified, using maximum likelihood methods. I show that genes under positive selection during human evolution are implicated in diseases such as epithelial cancers, schizophrenia, autoimmune diseases and Alzheimer’s disease. Comparisons of humans with great apes have shown such diseases to display biomedical disease differences, such as varying degrees of pathology, differing
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...dard mammalian species tree was trimmed to only include the species in the alignment using prunetree (Ziheng Yang, unpublished). The gene trees were created from the nucleotide alignment using phyml (=-=Guindon et al., 2005-=-) with model TN93 (Tamura and Nei, 1993) and 4 rate categories in the discrete gamma models of rate variation among sites (Yang, 1994). 149Figure 6.4 Example of a species tree (A) and a gene tree (B)...

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