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SynthHotSpot SIGNED

Synthesizing Meiotic Crossover Hotspots in Arabidopsis

Total Cost €

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EC-Contrib. €

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Partnership

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 SynthHotSpot project word cloud

Explore the words cloud of the SynthHotSpot project. It provides you a very rough idea of what is the project "SynthHotSpot" about.

evolutionary    homologous    crossover    narrow    recombination    crops    genetic    loci    epigenetic    patterns    species    genome    mapping    delete    rationally    direct    chromatin    ctt    technologies    hotspots    exchange    crossovers    structures    functional    effect    de    recombinant    epigenetically    pair    amplification    cas9    combinations    models    distributions    combined    engineering    methylation    breeding    tools    correct    silence    sexual    individual    genomics    revealed    dissect    detecting    termed    directing    editing    polymorphisms    signatures    novo    resolution    extensive    molecules    dna    hotspot    meiosis    comprehensively    random    understand    undergo    locations    majority    versus    accelerate    meiotic    strategic    proof    motifs    driving    reciprocal    natural    arabidopsis    first    patterning    gamete    profound    profile    repeat    definitive    sequencing    limiting    chromosomal    force    genetics    final    eukaryotes    chromosomes    proteins    sequence    fine    reproduce    diversity    talens    crispr    sexually   

Project "SynthHotSpot" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website https://www.plantsci.cam.ac.uk/directory/henderson-ian
 Total cost 1˙999˙953 €
 EC max contribution 1˙999˙953 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-CoG
 Funding Scheme ERC-COG
 Starting year 2016
 Duration (year-month-day) from 2016-10-01   to  2021-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 1˙999˙953.00

Map

 Project objective

The majority of eukaryotes reproduce sexually via meiosis. During meiosis homologous chromosomes pair and undergo reciprocal genetic exchange termed crossover. Meiotic recombination is a major evolutionary force and has a profound effect on patterns of genetic diversity in sexual species. Crossovers distributions are highly non-random and are typically focused in narrow hotspots. Study of hotspots throughout eukaryotes has revealed combinations of genetic and epigenetic factors that contribute to their distributions. In this proposal we will use the extensive genetics and genomics tools available in Arabidopsis to comprehensively dissect hotspot patterning. The strategic aim of the proposal is to use this knowledge to direct de novo hotspots to loci of choice. In the first aim we will use functional genomics to profile the chromosomal distributions of key recombination proteins and test the role of chromatin and higher-order structures in driving these patterns. In the second aim we will study individual hotspots at the fine-scale, to the resolution of individual polymorphisms, using amplification and sequencing of recombinant molecules from gamete DNA. To test genetic versus epigenetic control of hotspots we will use genome-editing to delete hotspot-associated CTT-repeat DNA sequence motifs, in addition to directing DNA methylation in order to epigenetically silence recombination. In the final aim we will use our combined knowledge of hotspot control to implement genome-editing technologies (TALENs & CRISPR-Cas9) during meiosis. This will allow us to rationally control hotspot locations, which will be definitive proof that our models for recombination control are correct. This technology will also accelerate breeding and genome-engineering of our most important crops, where recombination can be limiting. Finally, mapping hotspots will allow us to better understand patterns of natural genetic diversity, including detecting the signatures of selection.

 Publications

year authors and title journal last update
List of publications.
2018 Heïdi Serra, Kyuha Choi, Xiaohui Zhao, Alexander R. Blackwell, Juhyun Kim, Ian R. Henderson
Interhomolog polymorphism shapes meiotic crossover within the Arabidopsis RAC1 and RPP13 disease resistance genes
published pages: e1007843, ISSN: 1553-7404, DOI: 10.1371/journal.pgen.1007843
PLOS Genetics 14/12 2020-01-22
2018 Kyuha Choi, Xiaohui Zhao, Andrew J. Tock, Christophe Lambing, Charles J. Underwood, Thomas J. Hardcastle, Heïdi Serra, Juhyun Kim, Hyun Seob Cho, Jaeil Kim, Piotr A. Ziolkowski, Nataliya E. Yelina, Ildoo Hwang, Robert A. Martienssen, Ian R. Henderson
Nucleosomes and DNA methylation shape meiotic DSB frequency in Arabidopsis thaliana transposons and gene regulatory regions
published pages: 532-546, ISSN: 1088-9051, DOI: 10.1101/gr.225599.117
Genome Research 28/4 2020-01-22
2018 Charles J. Underwood, Kyuha Choi, Christophe Lambing, Xiaohui Zhao, Heïdi Serra, Filipe Borges, Joe Simorowski, Evan Ernst, Yannick Jacob, Ian R. Henderson, Robert A. Martienssen
Epigenetic activation of meiotic recombination near Arabidopsis thaliana centromeres via loss of H3K9me2 and non-CG DNA methylation
published pages: 519-531, ISSN: 1088-9051, DOI: 10.1101/gr.227116.117
Genome Research 28/4 2020-01-22
2018 Heïdi Serra, Christophe Lambing, Catherine H. Griffin, Stephanie D. Topp, Divyashree C. Nageswaran, Charles J. Underwood, Piotr A. Ziolkowski, Mathilde Séguéla-Arnaud, Joiselle B. Fernandes, Raphaël Mercier, Ian R. Henderson
Massive crossover elevation via combination of HEI10 and recq4a recq4b during Arabidopsis meiosis
published pages: 2437-2442, ISSN: 0027-8424, DOI: 10.1073/pnas.1713071115
Proceedings of the National Academy of Sciences 115/10 2020-01-22

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