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Plant Genome Mapping Laboratory

About: Plant Genome Mapping Laboratory is a based out in . It is known for research contribution in the topics: Genome & Gene. The organization has 179 authors who have published 264 publications receiving 22415 citations.


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Journal ArticleDOI
TL;DR: The MCScanX toolkit implements an adjusted MCScan algorithm for detection of synteny and collinearity that extends the original software by incorporating 14 utility programs for visualization of results and additional downstream analyses.
Abstract: MCScan is an algorithm able to scan multiple genomes or subgenomes in order to identify putative homologous chromosomal regions, and align these regions using genes as anchors. The MCScanX toolkit implements an adjusted MCScan algorithm for detection of synteny and collinearity that extends the original software by incorporating 14 utility programs for visualization of results and additional downstream analyses. Applications of MCScanX to several sequenced plant genomes and gene families are shown as examples. MCScanX can be used to effectively analyze chromosome structural changes, and reveal the history of gene family expansions that might contribute to the adaptation of lineages and taxa. An integrated view of various modes of gene duplication can supplement the traditional gene tree analysis in specific families. The source code and documentation of MCScanX are freely available at http://chibba.pgml.uga.edu/mcscan2/.

3,388 citations

Journal ArticleDOI
Boulos Chalhoub1, Shengyi Liu2, Isobel A. P. Parkin3, Haibao Tang4, Haibao Tang5, Xiyin Wang6, Julien Chiquet1, Harry Belcram1, Chaobo Tong2, Birgit Samans7, Margot Correa8, Corinne Da Silva8, Jérémy Just1, Cyril Falentin9, Chu Shin Koh10, Isabelle Le Clainche1, Maria Bernard8, Pascal Bento8, Benjamin Noel8, Karine Labadie8, Adriana Alberti8, Mathieu Charles9, Dominique Arnaud1, Hui Guo6, Christian Daviaud, Salman Alamery11, Kamel Jabbari12, Kamel Jabbari1, Meixia Zhao13, Patrick P. Edger14, Houda Chelaifa1, David C. Tack15, Gilles Lassalle9, Imen Mestiri1, Nicolas Schnel9, Marie-Christine Le Paslier9, Guangyi Fan, Victor Renault16, Philippe E. Bayer11, Agnieszka A. Golicz11, Sahana Manoli11, Tae-Ho Lee6, Vinh Ha Dinh Thi1, Smahane Chalabi1, Qiong Hu2, Chuchuan Fan17, Reece Tollenaere11, Yunhai Lu1, Christophe Battail8, Jinxiong Shen17, Christine Sidebottom10, Xinfa Wang2, Aurélie Canaguier1, Aurélie Chauveau9, Aurélie Bérard9, G. Deniot9, Mei Guan18, Zhongsong Liu18, Fengming Sun, Yong Pyo Lim19, Eric Lyons20, Christopher D. Town5, Ian Bancroft21, Xiaowu Wang, Jinling Meng17, Jianxin Ma13, J. Chris Pires22, Graham J.W. King23, Dominique Brunel9, Régine Delourme9, Michel Renard9, Jean-Marc Aury8, Keith L. Adams15, Jacqueline Batley11, Jacqueline Batley24, Rod J. Snowdon7, Jörg Tost, David Edwards24, David Edwards11, Yongming Zhou17, Wei Hua2, Andrew G. Sharpe10, Andrew H. Paterson6, Chunyun Guan18, Patrick Wincker1, Patrick Wincker25, Patrick Wincker8 
22 Aug 2014-Science
TL;DR: The polyploid genome of Brassica napus, which originated from a recent combination of two distinct genomes approximately 7500 years ago and gave rise to the crops of rape oilseed, is sequenced.
Abstract: Oilseed rape (Brassica napus L.) was formed ~7500 years ago by hybridization between B. rapa and B. oleracea, followed by chromosome doubling, a process known as allopolyploidy. Together with more ancient polyploidizations, this conferred an aggregate 72× genome multiplication since the origin of angiosperms and high gene content. We examined the B. napus genome and the consequences of its recent duplication. The constituent An and Cn subgenomes are engaged in subtle structural, functional, and epigenetic cross-talk, with abundant homeologous exchanges. Incipient gene loss and expression divergence have begun. Selection in B. napus oilseed types has accelerated the loss of glucosinolate genes, while preserving expansion of oil biosynthesis genes. These processes provide insights into allopolyploid evolution and its relationship with crop domestication and improvement.

1,743 citations

Journal ArticleDOI
27 Mar 2003-Nature
TL;DR: It is shown that a genome-wide duplication post-dates the divergence of Arabidopsis from most dicots, and that additional, more ancient duplication events affect more distant taxonomic comparisons.
Abstract: Conservation of gene order in vertebrates is evident after hundreds of millions of years of divergence, but comparisons of the Arabidopsis thaliana sequence to partial gene orders of other angiosperms (flowering plants) sharing common ancestry approximately 170-235 million years ago yield conflicting results. This difference may be largely due to the propensity of angiosperms to undergo chromosomal duplication ('polyploidization') and subsequent gene loss ('diploidization'); these evolutionary mechanisms have profound consequences for comparative biology. Here we integrate a phylogenetic approach (relating chromosomal duplications to the tree of life) with a genomic approach (mitigating information lost to diploidization) to show that a genome-wide duplication post-dates the divergence of Arabidopsis from most dicots. We also show that an inferred ancestral gene order for Arabidopsis reveals more synteny with other dicots (exemplified by cotton), and that additional, more ancient duplication events affect more distant taxonomic comparisons. By using partial sequence data for many diverse taxa to better relate the evolutionary history of completely sequenced genomes to the tree of life, we foster comparative approaches to the study of genome organization, consequences of polyploidy, and the molecular basis of quantitative traits.

1,420 citations

Journal ArticleDOI
20 Dec 2012-Nature
TL;DR: It is shown that an abrupt five- to sixfold ploidy increase approximately 60 million years (Myr) ago, and allopolyploidy reuniting divergent Gossypium genomes approximately 1–2 Myr ago, conferred about 30–36-fold duplication of ancestral angiosperm genes in elite cottons, genetic complexity equalled only by Brassica among sequenced angiosperms.
Abstract: Polyploidy often confers emergent properties, such as the higher fibre productivity and quality of tetraploid cottons than diploid cottons bred for the same environments. Here we show that an abrupt five- to sixfold ploidy increase approximately 60 million years (Myr) ago, and allopolyploidy reuniting divergent Gossypium genomes approximately 1-2 Myr ago, conferred about 30-36-fold duplication of ancestral angiosperm (flowering plant) genes in elite cottons (Gossypium hirsutum and Gossypium barbadense), genetic complexity equalled only by Brassica among sequenced angiosperms. Nascent fibre evolution, before allopolyploidy, is elucidated by comparison of spinnable-fibred Gossypium herbaceum A and non-spinnable Gossypium longicalyx F genomes to one another and the outgroup D genome of non-spinnable Gossypium raimondii. The sequence of a G. hirsutum A(t)D(t) (in which 't' indicates tetraploid) cultivar reveals many non-reciprocal DNA exchanges between subgenomes that may have contributed to phenotypic innovation and/or other emergent properties such as ecological adaptation by polyploids. Most DNA-level novelty in G. hirsutum recombines alleles from the D-genome progenitor native to its New World habitat and the Old World A-genome progenitor in which spinnable fibre evolved. Coordinated expression changes in proximal groups of functionally distinct genes, including a nuclear mitochondrial DNA block, may account for clusters of cotton-fibre quantitative trait loci affecting diverse traits. Opportunities abound for dissecting emergent properties of other polyploids, particularly angiosperms, by comparison to diploid progenitors and outgroups.

1,015 citations

Journal ArticleDOI
TL;DR: Integration of structural genomic data from a largely assembled rice genome sequence, with phylogenetic analysis of sequence samples for many other taxa, suggests that a polyploidization event occurred approximately 70 million years ago, before the divergence of the major cereals from one another but after the divergence from the Poales from the Liliales and Zingiberales.
Abstract: Integration of structural genomic data from a largely assembled rice genome sequence, with phylogenetic analysis of sequence samples for many other taxa, suggests that a polyploidization event occurred ≈70 million years ago, before the divergence of the major cereals from one another but after the divergence of the Poales from the Liliales and Zingiberales. Ancient polyploidization and subsequent “diploidization” (loss) of many duplicated gene copies has thus shaped the genomes of all Poaceae cereal, forage, and biomass crops. The Poaceae appear to have evolved as separate lineages for ≈50 million years, or two-thirds of the time since the duplication event. Chromosomes that are predicted to be homoeologs resulting from this ancient duplication event account for a disproportionate share of incongruent loci found by comparison of the rice sequence to a detailed sorghum sequence-tagged site-based genetic map. Differential gene loss during diploidization may have contributed many of these incongruities. Such predicted homoeologs also account for a disproportionate share of duplicated sorghum loci, further supporting the hypothesis that the polyploidization event was common to sorghum and rice. Comparative gene orders along paleo-homoeologous chromosomal segments provide a means to make phylogenetic inferences about chromosome structural rearrangements that differentiate among the grasses. Superimposition of the timing of major duplication events on taxonomic relationships leads to improved understanding of comparative gene orders, enhancing the value of data from botanical models for crop improvement and for further exploration of genomic biodiversity. Additional ancient duplication events probably remain to be discovered in other angiosperm lineages.

942 citations


Authors

Showing all 179 results

NameH-indexPapersCitations
Andrew H. Paterson11949659373
Nils Stein7323821040
Hari D. Upadhyaya6236015276
Ray Ming6126816790
Christian J. Stoeckert5917621076
Zhikang Li5516313377
Haibao Tang5513722306
Jessica C. Kissinger5415913335
John E. Bowers518816918
Shahid Mansoor482519263
Xiyin Wang4110519201
Xavier Draye381295917
Changsoo Kim341164721
Brad Chapman336711424
Brian P. Brunk33518289
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202115
202017
201914
201810
201719
201617