Timothy W. Chumley
University of Texas at Austin
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Featured researches published by Timothy W. Chumley.
Proceedings of the National Academy of Sciences of the United States of America | 2007
Robert K. Jansen; Zhengqiu Cai; Linda A. Raubeson; Henry Daniell; W Claude; Jim Leebens-Mack; Mary Guisinger-Bellian; Rosemarie C. Haberle; Anne Hansen; Timothy W. Chumley; Seung-Bum Lee; Rhiannon Peery; Joel R. McNeal; Jennifer V. Kuehl; Jeffrey L. Boore
Angiosperms are the largest and most successful clade of land plants with >250,000 species distributed in nearly every terrestrial habitat. Many phylogenetic studies have been based on DNA sequences of one to several genes, but, despite decades of intensive efforts, relationships among early diverging lineages and several of the major clades remain either incompletely resolved or weakly supported. We performed phylogenetic analyses of 81 plastid genes in 64 sequenced genomes, including 13 new genomes, to estimate relationships among the major angiosperm clades, and the resulting trees are used to examine the evolution of gene and intron content. Phylogenetic trees from multiple methods, including model-based approaches, provide strong support for the position of Amborella as the earliest diverging lineage of flowering plants, followed by Nymphaeales and Austrobaileyales. The plastid genome trees also provide strong support for a sister relationship between eudicots and monocots, and this group is sister to a clade that includes Chloranthales and magnoliids. Resolution of relationships among the major clades of angiosperms provides the necessary framework for addressing numerous evolutionary questions regarding the rapid diversification of angiosperms. Gene and intron content are highly conserved among the early diverging angiosperms and basal eudicots, but 62 independent gene and intron losses are limited to the more derived monocot and eudicot clades. Moreover, a lineage-specific correlation was detected between rates of nucleotide substitutions, indels, and genomic rearrangements.
Methods in Enzymology | 2005
Robert K. Jansen; Linda A. Raubeson; Jeffrey L. Boore; Claude W. dePamphilis; Timothy W. Chumley; Rosemarie C. Haberle; Stacia K. Wyman; Andrew J. Alverson; Rhiannon Peery; Sallie J. Herman; H. Matthew Fourcade; Jennifer V. Kuehl; Joel R. McNeal; Jim Leebens-Mack; Liying Cui
During the past decade, there has been a rapid increase in our understanding of plastid genome organization and evolution due to the availability of many new completely sequenced genomes. There are 45 complete genomes published and ongoing projects are likely to increase this sampling to nearly 200 genomes during the next 5 years. Several groups of researchers including ours have been developing new techniques for gathering and analyzing entire plastid genome sequences and details of these developments are summarized in this chapter. The most important developments that enhance our ability to generate whole chloroplast genome sequences involve the generation of pure fractions of chloroplast genomes by whole genome amplification using rolling circle amplification, cloning genomes into Fosmid or bacterial artificial chromosome (BAC) vectors, and the development of an organellar annotation program (Dual Organellar GenoMe Annotator [DOGMA]). In addition to providing details of these methods, we provide an overview of methods for analyzing complete plastid genome sequences for repeats and gene content, as well as approaches for using gene order and sequence data for phylogeny reconstruction. This explosive increase in the number of sequenced plastid genomes and improved computational tools will provide many insights into the evolution of these genomes and much new data for assessing relationships at deep nodes in plants and other photosynthetic organisms.
Journal of Molecular Evolution | 2010
Mary M. Guisinger; Timothy W. Chumley; Jennifer V. Kuehl; Jeffrey L. Boore; Robert K. Jansen
Plastid genomes of the grasses (Poaceae) are unusual in their organization and rates of sequence evolution. There has been a recent surge in the availability of grass plastid genome sequences, but a comprehensive comparative analysis of genome evolution has not been performed that includes any related families in the Poales. We report on the plastid genome of Typha latifolia, the first non-grass Poales sequenced to date, and we present comparisons of genome organization and sequence evolution within Poales. Our results confirm that grass plastid genomes exhibit acceleration in both genomic rearrangements and nucleotide substitutions. Poaceae have multiple structural rearrangements, including three inversions, three genes losses (accD, ycf1, ycf2), intron losses in two genes (clpP, rpoC1), and expansion of the inverted repeat (IR) into both large and small single-copy regions. These rearrangements are restricted to the Poaceae, and IR expansion into the small single-copy region correlates with the phylogeny of the family. Comparisons of 73 protein-coding genes for 47 angiosperms including nine Poaceae genera confirm that the branch leading to Poaceae has significantly accelerated rates of change relative to other monocots and angiosperms. Furthermore, rates of sequence evolution within grasses are lower, indicating a deceleration during diversification of the family. Overall there is a strong correlation between accelerated rates of genomic rearrangements and nucleotide substitutions in Poaceae, a phenomenon that has been noted recently throughout angiosperms. The cause of the correlation is unknown, but faulty DNA repair has been suggested in other systems including bacterial and animal mitochondrial genomes.
Molecular Biology and Evolution | 2005
Jim Leebens-Mack; Linda A. Raubeson; Liying Cui; Jennifer V. Kuehl; Matthew H. Fourcade; Timothy W. Chumley; Jeffrey L. Boore; Robert K. Jansen; Claude W. dePamphilis
Molecular Biology and Evolution | 2006
Timothy W. Chumley; Jeffrey D. Palmer; Jeffrey P. Mower; H. Matthew Fourcade; Patrick J. Calie; Jeffrey L. Boore; Robert K. Jansen
BMC Genomics | 2007
Linda A. Raubeson; Rhiannon Peery; Timothy W. Chumley; Chris Dziubek; H. Matthew Fourcade; Jeffrey L. Boore; Robert K. Jansen
Molecular Biology and Evolution | 2007
Hae Lim Lee; Robert K. Jansen; Timothy W. Chumley; Ki Joong Kim
Lawrence Berkeley National Laboratory | 2007
Linda A. Raubeso; Rhiannon Peery; Timothy W. Chumley; Chris Dziubek; H. Matthew Fourcade; Jeffrey L. Boore; Robert K. Jansen
Lawrence Berkeley National Laboratory | 2006
Timothy W. Chumley; Jeffrey D. Palmer; Jeffrey P. Mower; H. Matthew Fourcade; Patrick J. Calie; Jeffrey L. Boore; Robert K. Jansen
Journal Name: Molecular Biology and Evolution, Oxford Press - ifaccepted; Journal Volume: 23; Journal Issue: 11; Related Information: Journal Publication Date: 11/2006 | 2006
Timothy W. Chumley; Jeffrey D. Palmer; Jeffrey P. Mower; H. Matthew Fourcade; Patrick J. Calie; Jeffrey L. Boore; Robert K. Jansen