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Dive into the research topics where Cymon J. Cox is active.

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Featured researches published by Cymon J. Cox.


Nature | 2006

Reconstructing the early evolution of Fungi using a six-gene phylogeny

Timothy Y. James; Frank Kauff; Conrad L. Schoch; P. Brandon Matheny; Cymon J. Cox; Gail Celio; Emily Fraker; Jolanta Miadlikowska; H. Thorsten Lumbsch; Alexandra Rauhut; A. Elizabeth Arnold; Anja Amtoft; Jason E. Stajich; Kentaro Hosaka; Gi-Ho Sung; Desiree Johnson; Michael Crockett; Manfred Binder; Judd M. Curtis; Jason C. Slot; Zheng Wang; Andrew W. Wilson; Arthur Schu; Joyce E. Longcore; David G. Porter; Peter M. Letcher; Martha J. Powell; John W. Taylor; Merlin M. White; Gareth W. Griffith

The ancestors of fungi are believed to be simple aquatic forms with flagellated spores, similar to members of the extant phylum Chytridiomycota (chytrids). Current classifications assume that chytrids form an early-diverging clade within the kingdom Fungi and imply a single loss of the spore flagellum, leading to the diversification of terrestrial fungi. Here we develop phylogenetic hypotheses for Fungi using data from six gene regions and nearly 200 species. Our results indicate that there may have been at least four independent losses of the flagellum in the kingdom Fungi. These losses of swimming spores coincided with the evolution of new mechanisms of spore dispersal, such as aerial dispersal in mycelial groups and polar tube eversion in the microsporidia (unicellular forms that lack mitochondria). The enigmatic microsporidia seem to be derived from an endoparasitic chytrid ancestor similar to Rozella allomycis, on the earliest diverging branch of the fungal phylogenetic tree.


Proceedings of the National Academy of Sciences of the United States of America | 2008

The archaebacterial origin of eukaryotes

Cymon J. Cox; Peter G. Foster; Robert P. Hirt; Simon R. Harris; T. Martin Embley

The origin of the eukaryotic genetic apparatus is thought to be central to understanding the evolution of the eukaryotic cell. Disagreement about the source of the relevant genes has spawned competing hypotheses for the origins of the eukaryote nuclear lineage. The iconic rooted 3-domains tree of life shows eukaryotes and archaebacteria as separate groups that share a common ancestor to the exclusion of eubacteria. By contrast, the eocyte hypothesis has eukaryotes originating within the archaebacteria and sharing a common ancestor with a particular group called the Crenarchaeota or eocytes. Here, we have investigated the relative support for each hypothesis from analysis of 53 genes spanning the 3 domains, including essential components of the eukaryotic nucleic acid replication, transcription, and translation apparatus. As an important component of our analysis, we investigated the fit between model and data with respect to composition. Compositional heterogeneity is a pervasive problem for reconstruction of ancient relationships, which, if ignored, can produce an incorrect tree with strong support. To mitigate its effects, we used phylogenetic models that allow for changing nucleotide or amino acid compositions over the tree and data. Our analyses favor a topology that supports the eocyte hypothesis rather than archaebacterial monophyly and the 3-domains tree of life.


Bioinformatics | 2009

Biopython: freely available Python tools for computational molecular biology and bioinformatics.

Peter J. A. Cock; Tiago Antao; Jeffrey T. Chang; Brad Chapman; Cymon J. Cox; Andrew Dalke; Iddo Friedberg; Thomas Hamelryck; Frank Kauff; Bartosz Wilczyński; Michiel J. L. de Hoon

Summary: The Biopython project is a mature open source international collaboration of volunteer developers, providing Python libraries for a wide range of bioinformatics problems. Biopython includes modules for reading and writing different sequence file formats and multiple sequence alignments, dealing with 3D macro molecular structures, interacting with common tools such as BLAST, ClustalW and EMBOSS, accessing key online databases, as well as providing numerical methods for statistical learning. Availability: Biopython is freely available, with documentation and source code at www.biopython.org under the Biopython license. Contact: All queries should be directed to the Biopython mailing lists, see www.biopython.org/wiki/[email protected].


Nature | 2013

An archaeal origin of eukaryotes supports only two primary domains of life

Tom A. Williams; Peter G. Foster; Cymon J. Cox; T. Martin Embley

The discovery of the Archaea and the proposal of the three-domains ‘universal’ tree, based on ribosomal RNA and core genes mainly involved in protein translation, catalysed new ideas for cellular evolution and eukaryotic origins. However, accumulating evidence suggests that the three-domains tree may be incorrect: evolutionary trees made using newer methods place eukaryotic core genes within the Archaea, supporting hypotheses in which an archaeon participated in eukaryotic origins by founding the host lineage for the mitochondrial endosymbiont. These results provide support for only two primary domains of life—Archaea and Bacteria—because eukaryotes arose through partnership between them.


Journal of Clinical Microbiology | 2004

Phylogeny and Evolution of Medical Species of Candida and Related Taxa: a Multigenic Analysis

Stephanie Diezmann; Cymon J. Cox; Gabriele Schönian; Rytas Vilgalys; Thomas G. Mitchell

ABSTRACT Hemiascomycetes are species of yeasts within the order Saccharomycetales. The order encompasses disparate genera with a variety of life styles, including opportunistic human pathogens (e.g., Candida albicans), plant pathogens (e.g., Eremothecium gossypii), and cosmopolitan yeasts associated with water and decaying vegetation. To analyze the phylogeny of medically important species of yeasts, we selected 38 human pathogenic and related strains in the order Saccharomycetales. The DNA sequences of six nuclear genes were analyzed by maximum likelihood and Bayesian phylogenetic methods. The maximum likelihood analysis of the combined data for all six genes resolved three major lineages with significant support according to Bayesian posterior probability. One clade was mostly comprised of pathogenic species of Candida. Another major group contained members of the family Metschnikowiaceae as a monophyletic group, three species of Debaryomyces, and strains of Candida guilliermondii. The third clade consisted exclusively of species of the family Saccharomycetaceae. Analysis of the evolution of key characters indicated that both codon reassignment and coenzyme Q9 likely had single origins with multiple losses. Tests of correlated character evolution revealed that these two traits evolved independently.


The Bryologist | 2000

Evolution of the major moss lineages: phylogenetic analyses based on multiple gene sequences and morphology

Angela E. Newton; Cymon J. Cox; Jeffrey G. Duckett; John A. Wheeler; Bernard Goffinet; Terry A. Hedderson; Brent D. Mishler

Abstract Evolutionary relationships of mosses are still poorly understood, with family, order, and subclass circumscription and relationships remaining especially obscure. Over the past decade, a considerable body of data has accumulated, including information on morphological, developmental, anatomical, and ultrastructural characteristics, as well as nucleotide sequences for a number of nuclear and plastid genes. We have combined data from these different sources to provide an overview of the relationships of the major lineages of mosses. We analyzed a data set that includes 33 moss species and ten outgroup taxa drawn from the liverworts, hornworts, and vascular plants. Molecular data consisted of nucleotide sequences from four DNA regions, (rbcL, trnL-trnF, rps4 and 18S). Morphological data included 41 characters of which many were derived from published anatomical and ultra-structural studies. Combining morphological and molecular data in the analyses showed that mosses, including Sphagnum, Takakia, Andreaea and Andreaeobryum, form a monophyletic group, provided improved resolution of higher level relationships, and further insight into evolutionary patterns in morphology.


Proceedings of the Royal Society of London B: Biological Sciences | 2012

A congruent phylogenomic signal places eukaryotes within the Archaea

Tom A. Williams; Peter G. Foster; Tom M. W. Nye; Cymon J. Cox; T. Martin Embley

Determining the relationships among the major groups of cellular life is important for understanding the evolution of biological diversity, but is difficult given the enormous time spans involved. In the textbook ‘three domains’ tree based on informational genes, eukaryotes and Archaea share a common ancestor to the exclusion of Bacteria. However, some phylogenetic analyses of the same data have placed eukaryotes within the Archaea, as the nearest relatives of different archaeal lineages. We compared the support for these competing hypotheses using sophisticated phylogenetic methods and an improved sampling of archaeal biodiversity. We also employed both new and existing tests of phylogenetic congruence to explore the level of uncertainty and conflict in the data. Our analyses suggested that much of the observed incongruence is weakly supported or associated with poorly fitting evolutionary models. All of our phylogenetic analyses, whether on small subunit and large subunit ribosomal RNA or concatenated protein-coding genes, recovered a monophyletic group containing eukaryotes and the TACK archaeal superphylum comprising the Thaumarchaeota, Aigarchaeota, Crenarchaeota and Korarchaeota. Hence, while our results provide no support for the iconic three-domain tree of life, they are consistent with an extended eocyte hypothesis whereby vital components of the eukaryotic nuclear lineage originated from within the archaeal radiation.


Systematic Botany | 2004

Chloroplast Phylogeny of Asplenioid Ferns based on rbcL and trnL-F Spacer Sequences (Polypodiidae, Aspleniaceae) and its Implications for Biogeography

Harald Schneider; Steve J. Russell; Cymon J. Cox; Freek T. Bakker; Sally Henderson; F. J. Rumsey; John A. Barrett; Mary Gibby; Johannes C. Vogel

Abstract Molecular phylogenies have been generated to investigate relationships among species and putative segregates in Asplenium, one of the largest genera in ferns. Of the ∼700 described taxa, 71 are included in a phylogenetic analysis using the chloroplast rbcL gene and trnL-F spacer. Our results support Hymenasplenium as the sister lineage to all other asplenioid ferns, and all other putative satellite genera are nested within this asplenioid clade. Instead of the classical and well-recognized separation into Old and New World clades, asplenioid ferns reveal a separation of the deeper branches into tropical and temperate clades. Temperate clades have evolved from tropical, more-basal clades and the phylogeny indicates up to six shifts between temperate and tropical preferences in the evolution of this widespread genus. Implications for speciation processes and biogeographic aspects, including the re-colonization of temperate regions after the last glacial period, are discussed and we present a phylogenetic framework from which the historical biogeography of asplenioid ferns can be inferred for Europe and North America.


Systematic Biology | 2014

Conflicting Phylogenies for Early Land Plants are Caused by Composition Biases among Synonymous Substitutions

Cymon J. Cox; Blaise Li; Peter G. Foster; T. Martin Embley; Peter Civáň

Plants are the primary producers of the terrestrial ecosystems that dominate much of the natural environment. Occurring approximately 480 Ma (Sanderson 2003; Kenrick et al. 2012), the evolutionary transition of plants from an aquatic to a terrestrial environment was accompanied by several major developmental innovations. The freshwater charophyte ancestors of land plants have a haplobiontic life cycle with a single haploid multicellular stage, whereas land plants, which include the bryophytes (liverworts, hornworts, and mosses) and tracheophytes (also called vascular plants, namely, lycopods, ferns, and seed plants), exhibit a marked alternation of generations with a diplobiontic life cycle with both haploid and diploid multicellular stages and where the embryo remains attached to, and is nourished by, the gametophyte (Haig 2008). The interjection of a multicellular diploid phase into the land–plant life cycle was an important adaptation that enabled long-distance dispersal via mitotic spores where waterborne male gametes have restricted motility in dry terrestrial environments. Despite the similarity among land–plant life cycles, they differ in one significant aspect: in the three bryophyte groups, the haploid gametophytic stage is the dominant vegetative stage, whereas in vascular plants the diploid sporophyte dominates. A common assumption, and one implied by the tradition of referring to bryophytes as “lower plants”—in contrast to the “higher” tracheophytes—is that the bryophytes and their life cycle are primitive (Kato and Akiyama 2005). However, without a strong phylogenetic hypothesis of land–plant relationships, it is not clear which (if either) of the gametophyte or sporophyte was the dominant ancestral vegetative state present in the earliest land plants (Renzaglia et al. 2007; Qiu et al. 2012).


American Journal of Botany | 2003

Polarity of peatmoss (Sphagnum) evolution: who says bryophytes have no roots?

A. Jonathan Shaw; Cymon J. Cox; Sandra B. Boles

The class Sphagnopsida (Bryophyta) includes two genera: Ambuchanania and Sphagnum. Ambuchanania contains just one rare species known from two Tasmanian localities, but Sphagnum comprises a speciose clade of mosses that dominates many wetland ecosystems, especially in the boreal zone of the Northern Hemisphere. Recent phylogenetic analyses have resolved well-supported clades within Sphagnum, but polarizing Sphagnum evolution has been problematic because the genus is so isolated that it is difficult to determine homologies between morphological and/or molecular traits within Sphagnum with those of any potential outgroup. DNA sequences from 16 genomic regions representing the mitochondrial, chloroplast, and nuclear genomes (ca. 16 kilobases) were obtained from 24 species of Sphagnum plus one species each from Takakia and Andreaea in order to resolve a rooted phylogeny. Two tropical species, S. sericeum and S. lapazense, were resolved as sister to the rest of the genus and are extremely divergent from all other sphagna. The main Sphagnum lineage consists of two clades; one includes the sections Sphagnum, Rigida, and Cuspidata, and the other includes Subsecunda, Acutifolia, and Squarrosa. The placement of section Subsecunda is weakly supported, but other nodes are strongly supported by maximum parsimony, maximum likelihood, and Bayesian analyses. In addition to homogeneous Bayesian analyses, heterogeneous models were employed to account for different patterns of nucleotide substitution among genomic regions.

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William R. Buck

New York Botanical Garden

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Rodrigo Costa

Instituto Superior Técnico

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