29 September 2011

Genetic library will speed up disease research

International consortium will reveal gene function from mouse genetics

The International Mouse Phenotyping Consortium launched officially on 29 September. The consortium seeks to develop a library of gene function through the study of knockout mice.

The International Mouse Phenotyping Consortium launched officially on 29 September. The consortium seeks to develop a library of gene function through the study of knockout mice.

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An international project to create one of the largest libraries of mammalian genetic function data is launched on 29 September 2011. The International Mouse Phenotyping Consortium (IMPC) is building a library of mammalian gene function that will describe the function of every gene in the mouse genome.

The IMPC programme will allow researchers from across the world to easily access all of the resources and information created by the programme in 'knockout mice' - that is, mice in which a gene has been inactivated in order to discover what that gene does. Around 99 per cent of the genes in a mouse have an equivalent in humans. By understanding the function of all the genes within the mouse, scientists can improve their understanding of the role that genes play in human diseases such as heart disease and diabetes.

The resource will substantially shorten the time between basic research and clinical application.

"Our drive is to understand the role of genes in disease and use that understanding to improve healthcare," explains Dr Bill Skarnes, Senior Investigator at the Wellcome Trust Sanger Institute, a leading partner in IMPC. "The cells and DNA resources we have developed for IMPC have already proved their value in identifying genes involved in a form of anaemia. The integrated resources delivered by IMPC will make a real difference to researchers' work around the world."

Funding has been awarded to members of the consortium by a number of national funding agencies: recently the US National Institutes of Health awarded US $110 m over five years to members of the consortium to work on the project. The first phase of this ten-year project will knock out 5000 mouse genes and describe their physical characteristics or phenotypes.

" Our drive is to understand the role of genes in disease and use that understanding to improve healthcare: the resources delivered by IMPC will make a real difference to researchers' work around the world. "

Dr Bill Skarnes

"We want to characterise each line of mice broadly with no assumptions about what the gene may be doing," explains Dr Mark Moore, IMPC Executive Director. "If you think of the function of a gene as a needle in a haystack, we're removing the haystack so scientists can see what the needle does," he added.

All members of the IMPC will use standard, agreed procedures to perform the biological investigations and the data will be deposited in a single international database. The set of tests is designed to give information on human disease, such as heart disease, diabetes, and deafness, and the results will determine if that gene has a part to play in those diseases. The mice and the data generated from them will be freely available to the scientific community.

Dr Francis Collins, Director of the National Institutes of Health, says: "The addition of detailed clinical information for each knockout mouse line will be a boon to disease researchers who want to determine the function of genes and improve mouse models of human disease."

"The IMPC will make a difference to the drive worldwide to understand the role of genes in health and human disease," explains Professor Allan Bradley, Principal Investigator on European and US Mouse Knockout programmes and Director Emeritus of the Wellcome Trust Sanger. "It is inclusive, coherent, accessible and comprehensive. It seeks to be the library of gene function that researchers will turn to and use time and time again."

Underpinning the IMPC project has been a lengthy period of planning and technical preparations. A fundamental component of this has been the planning for a data coordination centre (DCC) which will allow unrestricted public access to IMPC data. Data generated by IMPC will be used by pharmaceutical and biotechnology companies to speed up the development pipeline of new drugs.

Dr Paul Flicek of EMBL-EBI added: "The open resources created by IMPC will be integrated with many other molecular databases at EMBL-EBI and elsewhere, and benefit from advanced search functionality. This will ensure that researchers can make use of detailed data and high-level summaries of mouse phenotypes and other relevant biological information - for example human disease associations - well into the future."

Notes to Editors

About the IMPC

The IMPC is a worldwide consortium comprising fifteen research institutions along with national funders from six countries, including the Medical Research Council (MRC) Harwell (UK), the National Institutes of Health (US), the Wellcome Trust Sanger Institute and EMBL-European Bioinformatics Institute in Hinxton (UK), Helmholtz Zentrum Munich, German Mouse Clinic (Germany), Toronto Centre for Phenogenomics (Canada), Institute Clinique de la Souris (France), Australian Phenomics Network, RIKEN BioResource Centre (Japan), CNR Monterotondo (Italy), Baylor College of Medicine (US), University of California Davis (US), Charles River Laboratories (US), Children's Hospital Oakland Research Institute (US), the Jackson Laboratories (US), Genome Canada (Canada), and MARC - Nanjing University (China). This strong international partnership hopes to increase its membership as the programme moves forward.
For more information on the IMPC go to www.mousephenotype.org

IMPC is building on the successful and ground-breaking EUMODIC project (funded by the European Commission under grant LSHG-CT-2006-037188) which developed the SOPs and IT systems needed to store the vast amounts of data generated and piloted the production and phenotyping of the mice. IMPC is therefore building upon years of planning and technical preparation.

Funding

KOMP2 and MPI2

The National Institutes of Health KOMP2 production and phenotyping awards. Each group will receive a total of approximately $34 million and is expected to produce and phenotype 833 strains of knockout mice over five years. Recipients of the awards are:

  • Baylor College of Medicine in Houston, TX (US). This centre will collaborate with the Wellcome Trust Sanger Institute (UK) and the Medical Research Council Harwell (UK)
  • University of California Davis, CA (US). This centre will collaborate with the Toronto Centre for Phenogenomics (Canada), Children's Hospital Oakland Research Institute, CA (US) and Charles River Laboratories in Wilmington, MA (US)
  • The Jackson Laboratory in Bar Harbor, MA (US)

Notes on DCC award (called MPI2). The National Institutes of Health awarded another five-year cooperative agreement totalling $10 million to the European Bioinformatics Institute and The Wellcome Trust Sanger Institute, UK and MRC Harwell, UK.

Medical Research Council

For almost 100 years the Medical Research Council has improved the health of people in the UK and around the world by supporting the highest quality science. The MRC invests in world-class scientists. It has produced 29 Nobel Prize winners and sustains a flourishing environment for internationally recognised research. The MRC focuses on making an impact and provides the financial muscle and scientific expertise behind medical breakthroughs, including one of the first antibiotics penicillin, the structure of DNA and the lethal link between smoking and cancer. Today MRC funded scientists tackle research into the major health challenges of the 21st century.
www.mrc.ac.uk

The European Bioinformatics Institute

The European Bioinformatics Institute (EBI, www.ebi.ac.uk) is part of the European Molecular Biology Laboratory (EMBL, www.embl.de) and is located on the Wellcome Trust Genome Campus in Hinxton near Cambridge (UK). The EBI grew out of EMBL's pioneering work in providing public biological databases to the research community. It hosts some of the world's most important collections of biological data, including DNA sequences (ENA), protein sequences (UniProt), animal genomes (Ensembl), 3D structures (the Protein Databank in Europe), data from gene expression experiments (ArrayExpress), protein-protein interactions (IntAct) and pathway information (Reactome). The EBI hosts several research groups and its scientists continually develop new tools for the biocomputing community. EMBL-EBI is coordinating ELIXIR (www.elixir-europe.org), a pan-European research infrastructure for biological information.

The Wellcome Trust Sanger Institute

The Wellcome Trust Sanger Institute is one of the world's leading genome centres. Through its ability to conduct research at scale, it is able to engage in bold and long-term exploratory projects that are designed to influence and empower medical science globally. Institute research findings, generated through its own research programmes and through its leading role in international consortia, are being used to develop new diagnostics and treatments for human disease.

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The Wellcome Trust

The Wellcome Trust is a global charitable foundation dedicated to achieving extraordinary improvements in human and animal health. We support the brightest minds in biomedical research and the medical humanities. Our breadth of support includes public engagement, education and the application of research to improve health. We are independent of both political and commercial interests.

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