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Researchers develop mouse genetic blueprint; Mouse study drives forward understanding of human biology

Date:
September 15, 2011
Source:
Wellcome Trust Sanger Institute
Summary:
Scientists have decoded and compared the genome sequence of 17 mouse strains, developing a valuable mouse genetic blueprint that will accelerate future research and understanding of human genetics. The team found an astonishing 56.7 million SNPs among the strains, in addition to other more complex differences, and used these sequence differences to uncover genetic associations with more than 700 biological differences, including markers for diseases such as diabetes and heart disease.

An overview of variants called from 17 mouse genomes relative to the reference. Four wild strains (CAST/EiJ, WSB/EiJ, PWK/PhJ and SPRET/EiJ) are shown in a circle with tracks indicating the relative density of single nucleotide polymophisms (SNPs), structural variants (SVs) and uncallable regions. Transposable element insertions (TEs), a subset of the SV calls, are shown as a separate track. Corresponding tracks are shown for each of the 13 classical laboratory strains to the right of the circle. Links crossing the circle indicate regions on the reference where the wild strain is closest to the reference.
Credit: From Keane et al. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature, 2011; 477 (7364): 289 DOI: 10.1038/nature10413

Researchers have developed a valuable mouse genetic blueprint that will accelerate future research and understanding of human genetics. The international team, led by researchers at the Wellcome Trust Sanger Institute and the University of Oxford, explains in two papers published in Nature on Sept. 14, 2011 how they decoded and compared the genome sequence of 17 mouse strains.

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In creating this unique resource, the biggest catalogue for any vertebrate model organism, the team found an astonishing 56.7 million unique sites of variation (known as SNPs) between the strains, in addition to other more complex differences. Among these they identified sequence differences associated with over 700 biological differences, including markers for diseases such as diabetes and heart disease, so linking genes with medically important individual differences.

The catalogue, which was funded principally by the Medical Research Council and the Wellcome Trust, can be used by researchers to understand the genetic basis of individual variation, and to ask fundamental questions about how genes function and make us more or less likely to have particular diseases.

Inbred strains of mice are invaluable sources of genetic information. Every animal within each inbred strain is essentially genetically identical, but each strain is different from the others both in their genes and across a huge range of medically and biologically important characteristics.

"We are living in an era where we have thousands of human genomes at our finger tips," says Dr Adams, from the Wellcome Trust Sanger Institute, who led the project. "The mouse, and the genome sequences we have generated, will play a critical role in understanding of how genetic variation contributes to disease and will lead us towards new therapies."

As a direct result of the project, researchers will place less reliance on breeding mice to find mutations; using this resource they will be able to find mutations much more quickly by the click of a digital mouse to search for the data on their computer.

These strains of mice are used in every corner of biology to further our understanding of human disease, and there is much more to discover. With the variants to hand, the challenge moves to understanding the biological consequences.

"In some cases it has taken 40 years -- an entire working life -- to pin down a gene in a mouse model that is associated with a human disease, looking for the cause," explains Dr Thomas Keane, who was first author on one of the papers. "Now with our catalogue of variants the analysis of these mice is breathtakingly fast and can be completed in the time it takes to make a cup of coffee.

"We now know where all the variants are, so the questions today are what do they do, and can we explain the phenotypic differences between different strains of mice?"

Crucially, the resource will reduce the amount of mouse breeding and testing needed to identify genes and mutations, reducing the numbers of mice required for each study. The initial discovery can be made computationally. The extensive catalogue will be invaluable for associating variation in a trait with changes to DNA -- the biologist's journey from phenotype to genotype.

Using the sequence of the 17 mouse genomes, the team looked for variants associated with quantitative trait loci (QTLs) implicating differences in the sequence between strains as being associated with the phenotypes that distinguish them.

"This study is a first step in a long path that moves from understanding what the genome is, to what it does," says Professor Jonathan Flint, from the Wellcome Trust Centre for Human Genetics, who co-led the study.

"The biological differences across the inbred strains of mice model variation between individual humans," says Professor Ian Jackson, joint head of Medical and Development Genetics at the Medical Research Council's Human Genetics Unit. "This resource, made possible through huge recent advances in sequencing technology, is transforming our understanding of how DNA sequence variation relates to gene function, and ultimately its association with biology and human health."

The project will be extended by sequencing further mouse strains, defining the genetic changes in mouse cancers and investigating the effect of variants on gene function.

The blueprint, coupled with today's speedier sequencing, enables researchers to probe deeper to find mutations affecting gene function at a much faster rate. It also opens the doorway to the possibility of sequencing much larger numbers of mice, with plans to extend the project to hundreds of mouse strains, a feat that only a few years ago would have seemed impossible.


Story Source:

The above story is based on materials provided by Wellcome Trust Sanger Institute. Note: Materials may be edited for content and length.


Journal References:

  1. Thomas M. Keane, Leo Goodstadt, Petr Danecek, Michael A. White, Kim Wong, Binnaz Yalcin, Andreas Heger, Avigail Agam, Guy Slater, Martin Goodson, Nicholas A. Furlotte, Eleazar Eskin, Christoffer Nellåker, Helen Whitley, James Cleak, Deborah Janowitz, Polinka Hernandez-Pliego, Andrew Edwards, T. Grant Belgard, Peter L. Oliver, Rebecca E. McIntyre, Amarjit Bhomra, Jérôme Nicod, Xiangchao Gan, Wei Yuan, Louise van der Weyden, Charles A. Steward, Sendu Bala, Jim Stalker, Richard Mott, Richard Durbin, Ian J. Jackson, Anne Czechanski, José Afonso Guerra-Assunção, Leah Rae Donahue, Laura G. Reinholdt, Bret A. Payseur, Chris P. Ponting, Ewan Birney, Jonathan Flint, David J. Adams. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature, 2011; 477 (7364): 289 DOI: 10.1038/nature10413
  2. Binnaz Yalcin, Kim Wong, Avigail Agam, Martin Goodson, Thomas M. Keane, Xiangchao Gan, Christoffer Nellåker, Leo Goodstadt, Jérôme Nicod, Amarjit Bhomra, Polinka Hernandez-Pliego, Helen Whitley, James Cleak, Rebekah Dutton, Deborah Janowitz, Richard Mott, David J. Adams, Jonathan Flint. Sequence-based characterization of structural variation in the mouse genome. Nature, 2011; 477 (7364): 326 DOI: 10.1038/nature10432

Cite This Page:

Wellcome Trust Sanger Institute. "Researchers develop mouse genetic blueprint; Mouse study drives forward understanding of human biology." ScienceDaily. ScienceDaily, 15 September 2011. <www.sciencedaily.com/releases/2011/09/110914131325.htm>.
Wellcome Trust Sanger Institute. (2011, September 15). Researchers develop mouse genetic blueprint; Mouse study drives forward understanding of human biology. ScienceDaily. Retrieved October 30, 2014 from www.sciencedaily.com/releases/2011/09/110914131325.htm
Wellcome Trust Sanger Institute. "Researchers develop mouse genetic blueprint; Mouse study drives forward understanding of human biology." ScienceDaily. www.sciencedaily.com/releases/2011/09/110914131325.htm (accessed October 30, 2014).

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