Gavin C. Conant

Gavin C. Conant

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Gavin C. Conant

Biomathematics Program, North Carolina State University, Raleigh, NC, U.S.A.

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 August 2011 in Nature Genetics
Verified
Journal Article
Closed access
PDF file
TCThe Brassica rapa Genome Sequencing Project Consortium
The Brassica rapa Genome Sequencing Project Consortium
XWXiaowu Wang
Xiaowu Wang
HWHanzhong Wang
Hanzhong Wang
JWJun Wang
Jun Wang
RSRifei Sun
Rifei Sun
ZZZhonghua Zhang
Zhonghua Zhang

1 December 2008 in Nature Reviews Genetics
Verified
Journal Article
Closed access
GCGavin C. Conant
Gavin C. Conant
KWKenneth H. Wolfe
Kenneth H. Wolfe

22 June 2015 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
PEPatrick P. Edger
Patrick P. Edger
HHHanna M. Heidel-Fischer
Hanna M. Heidel-Fischer
MBMichaël Bekaert
Michaël Bekaert
JRJadranka Rota
Jadranka Rota
GGGernot Glöckner
Gernot Glöckner
CWChristopher W. Wheat
Christopher W. Wheat
Significance: This research uncovers the mechanisms of an ancient arms race between butterflies and plants, seen today in countless gardens as caterpillars of cabbage butterflies that devour cabbage crop varieties. Nearly 90 million years ago, the ancestors of Brassica (mustards, cabbage) and related plants developed a chemical defense called glucosinolates. While very toxic to most insects, humans experience glucosinolates as the sharp taste in wasabi, horseradish and mustard. Here we report that this triggered a chemical arms race that escalated in complexity over time. By investigating the evolutionary histories of these plants and insects, we found that major increases in chemical defense complexity were followed by butterflies evolving countertactics to allow them to continue to attack and feed on the plants.

28 January 2008 in Bioinformatics
Verified
Journal Article
Open access
PDF file
GCGavin C. Conant
Gavin C. Conant
KWKenneth H. Wolfe
Kenneth H. Wolfe
We describe GenomeVx, a web-based tool for making editable, publication-quality, maps of mitochondrial and chloroplast genomes and of large plasmids. These maps show the location of genes and chromosomal features as well as a position scale. The program takes as input either raw feature positions or GenBank records. In the latter case, features are automatically extracted and colored, an example of which is given. Output is in the Adobe Portable Document Format (PDF) and can be edited by programs such as Adobe Illustrator. Availability: GenomeVx is available at http://wolfe.gen.tcd.ie/GenomeVx Contact:conantg@tcd.ie

1 June 2014 in Current Opinion in Plant Biology
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Journal Article
Closed access
GCGavin C Conant
Gavin C Conant
JBJames Birchler
James Birchler
JPJ Chris Pires
J Chris Pires

15 May 2007 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
DSDevin R. Scannell
Devin R. Scannell
AFA. Carolin Frank
A. Carolin Frank
GCGavin C. Conant
Gavin C. Conant
KBKevin P. Byrne
Kevin P. Byrne
MWMegan Woolfit
Megan Woolfit
KWKenneth H. Wolfe
Kenneth H. Wolfe
Among yeasts that underwent whole-genome duplication (WGD), Kluyveromyces polysporus represents the lineage most distant from Saccharomyces cerevisiae . By sequencing the K. polysporus genome and comparing it with the S. cerevisiae genome using a likelihood model of gene loss, we show that these species diverged very soon after the WGD, when their common ancestor contained >9,000 genes. The two genomes subsequently converged onto similar current sizes (5,600 protein-coding genes each) and independently retained sets of duplicated genes that are strikingly similar. Almost half of their surviving single-copy genes are not orthologs but paralogs formed by WGD, as would be expected if most gene pairs were resolved independently. In addition, by comparing the pattern of gene loss among K. polysporus , S. cerevisiae , and three other yeasts that diverged after the WGD, we show that the patterns of gene loss changed over time. Initially, both members of a duplicate pair were equally likely to be lost, but loss of the same gene copy in independent lineages was increasingly favored at later time points. This trend parallels an increasing restriction of reciprocal gene loss to more slowly evolving gene pairs over time and suggests that, as duplicate genes diverged, one gene copy became favored over the other. The apparent low initial sequence divergence of the gene pairs leads us to propose that the yeast WGD was probably an autopolyploidization.