Thomas Henry Noel Ellis

Dr. Thomas Henry Noel Ellis


Research Focus & Metrics

Academic Career Length

46Years (1981-Present)

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

Representative Publications

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2 September 2019 in Nature Genetics
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Journal Article
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JKJonathan Kreplak
Jonathan Kreplak
MMMohammed-Amin Madoui
Mohammed-Amin Madoui
PCPetr Cápal
Petr Cápal
PNPetr Novak
Petr Novak
KLKarine Labadie
Karine Labadie
JBJudith Burstin
Judith Burstin
We report the first annotated chromosome-level reference genome assembly for pea, Gregor Mendel’s original genetic model. Phylogenetics and paleogenomics show genomic rearrangements across legumes and suggest a major role for repetitive elements in pea genome evolution. Compared to other sequenced Leguminosae genomes, the pea genome shows intense gene dynamics, most likely associated with genome size expansion when the Fabeae diverged from its sister tribes. During Pisum evolution, translocation and transposition differentially occurred across lineages. This reference sequence will accelerate our understanding of the molecular basis of agronomically important traits and support crop improvement.

1 January 1990 in Cell
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Journal Article
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MBMadan K. Bhattacharyya
Madan K. Bhattacharyya
ASAlison M. Smith
Alison M. Smith
TEThomas Henry Noel Ellis
Thomas Henry Noel Ellis
CHCliff Hedley
Cliff Hedley
CMCathie Martin
Cathie Martin

15 October 2004 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
HCHong-Kyu Choi
Hong-Kyu Choi
JMJeong-Hwan Mun
Jeong-Hwan Mun
DKDong-Jin Kim
Dong-Jin Kim
HZHongyan Zhu
Hongyan Zhu
JBJong-Min Baek
Jong-Min Baek
Douglas CookDouglas Cook
Douglas Cook
Legumes are simultaneously one of the largest families of crop plants and a cornerstone in the biological nitrogen cycle. We combined molecular and phylogenetic analyses to evaluate genome conservation both within and between the two major clades of crop legumes. Genetic mapping of orthologous genes identifies broad conservation of genome macrostructure, especially within the galegoid legumes, while also highlighting inferred chromosomal rearrangements that may underlie the variation in chromosome number between these species. As a complement to comparative genetic mapping, we compared sequenced regions of the model legume Medicago truncatula with those of the diploid Lotus japonicus and the polyploid Glycine max . High conservation was observed between the genomes of M. truncatula and L. japonicus , whereas lower levels of conservation were evident between M. truncatula and G. max . In all cases, conserved genome microstructure was punctuated by significant structural divergence, including frequent insertion/deletion of individual genes or groups of genes and lineage-specific expansion/contraction of gene families. These results suggest that comparative mapping may have considerable utility for basic and applied research in the legumes, although its predictive value is likely to be tempered by phylogenetic distance and genome duplication.

1 August 1997 in Current Biology
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Journal Article
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JHJulie Margareth Isabel Hofer
Julie Margareth Isabel Hofer
LTLynda Turner
Lynda Turner
RHRoger Hellens
Roger Hellens
MAMike Ambrose
Mike Ambrose
PMPeter Matthews
Peter Matthews
TEThomas Henry Noel Ellis
Thomas Henry Noel Ellis

1 April 2005 in Plant Physiology
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Journal Article
Closed access
VHValérie Hecht
Valérie Hecht
FFFabrice Foucher
Fabrice Foucher
Cristina FerrandizCristina Ferrandiz
Cristina Ferrandiz
RMRichard Macknight
Richard Macknight
CNCristina Navarro
Cristina Navarro
JWJames L. Weller
James L. Weller
The model plants Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) have provided a wealth of information about genes and genetic pathways controlling the flowering process, but little is known about the corresponding pathways in legumes. The garden pea (Pisum sativum) has been used for several decades as a model system for physiological genetics of flowering, but the lack of molecular information about pea flowering genes has prevented direct comparison with other systems. To address this problem, we have searched expressed sequence tag and genome sequence databases to identify flowering-gene-related sequences from Medicago truncatula, soybean (Glycine max), and Lotus japonicus, and isolated corresponding sequences from pea by degenerate-primer polymerase chain reaction and library screening. We found that the majority of Arabidopsis flowering genes are represented in pea and in legume sequence databases, although several gene families, including the MADS-box, CONSTANS, and FLOWERING LOCUS T/TERMINAL FLOWER1 families, appear to have undergone differential expansion, and several important Arabidopsis genes, including FRIGIDA and members of the FLOWERING LOCUS C clade, are conspicuously absent. In several cases, pea and Medicago orthologs are shown to map to conserved map positions, emphasizing the closely syntenic relationship between these two species. These results demonstrate the potential benefit of parallel model systems for an understanding of flowering phenology in crop and model legume species.

4 August 2010 in Heredity
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Journal Article
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Ruslan KalendarRuslan Kalendar
Ruslan Kalendar
AFA J Flavell
A J Flavell
TEThomas Henry Noel Ellis
Thomas Henry Noel Ellis
TST Sjakste
T Sjakste
CMCédric Moisy
Cédric Moisy
Alan H. SchulmanAlan H. Schulman
Alan H. Schulman