Knockout mouse resource reveals genes and pathways linked to human disease
News / Published: 19 July 2013
Researchers have switched off more than 900 genes in mice, one at a time, to create a new resource that will reveal which genes are important for a wide range of biological functions such as fertility and hearing.
The new genetically modified mouse strains are now openly available to research groups worldwide to encourage continued work to understand the fundamental mechanisms of human and animal disease.
The resource, which is known as the Mouse Genetics Project, screens for signs of disease and has revealed many new functions for well-known genes, as well as for genes with no previously known role in disease. Many of these variations in body function are likely to underlie human diseases.
The human genome has more than 20,000 identified genes, but our understanding of what they do and how disease results when they malfunction is limited. Studies using mice are vital to help us understand how genes function and how variations in genes cause disease. Mice share the vast majority of their genes with humans, and researchers can use mice that have a specific gene switched off to start to unravel human disease.
The Mouse Genetics Project provides researchers and clinicians with a wealth of freely available clinical and biological information that will help find new treatments and options for a wide range of human diseases.
"Our project has revealed many completely unexpected associations between genes and traits like body weight, emphasising how difficult it is to predict the importance of a gene in disease until there is a model like the mouse to give us clues," says Professor Karen Steel, lead author from King's College London and Honorary Faculty at the Wellcome Trust Sanger Institute.
"There are many paths to developing a disease that aren't immediately obvious. This resource provides an efficient way to uncover these paths. This resource is the largest collection of mouse lines available to researchers where all other genes are virtually identical except the gene switched off.
"Together with the careful optimisation of their environment and the systematic analysis of a wide range of characteristics in each line, we are able to detect features that otherwise would be missed."
So far, the team have individually switched off more than 900 genes in mice to understand how they function and how they relate to disease. Rather than focus on one or two potential effects, the team are systematically studying a large number of potential outcomes to build a catalogue of gene functions and effects.
The new report published today describes the detailed analysis of the first 250 lines to undergo this systematic health screen.
The researchers discovered that newly identified and unknown genes are just as likely to underlie disease features as known genes. This finding emphasises the value of a broad approach to studying diseases, rather than the current tendency to focus on well-known genes. The availability of mouse models and publicly available information about their characteristics should encourage a broader understanding of the full extent of gene function and how genetic changes can result in disease.
The team revealed that a gene, Kptn, previously thought to be linked to deafness could actually be associated with obesity. They found that when the gene is switched off in mice fed a high-fat diet, the mice gain weight faster than those that have working copies of the gene. This is one of the many examples of genes identified by the team to have a surprising new role in disease.
Among the genes reported in detail are 26 brand new mouse models for human diseases, allowing detailed investigation of the underlying biology of these diseases. For example, variations to the gene SMS can cause a rare, inherited condition associated with both mental and physical difficulties, known as Snyder-Robinson syndrome.
The team switched off the same gene in mice, and the results reproduced those seen in the human disease. They also detected male infertility, suggesting a new feature of the disease that may not have been recognised in humans with SMS mutations.
"Not only is the biological information openly available to the wider scientific and clinical community, but so are our mouse models," says Dr Jacqui White, first author from the Wellcome Trust Sanger Institute. "Already 447 research teams in 25 different countries across the world are using our mouse lines and taking this research to new levels. Our hope is that other research teams will take our research forward to better understand disease and develop new and effective therapies against these diseases."
“This resource is revealing a wealth of information about human disease that has great potential for improved diagnosis and treatment options," says Professor Philip Beales, Professor of Medical Genetics at the Institute of Child Health, UCL, and a consultant clinical geneticist at Guy's Hospital and Great Ormond Street Hospital. "This is just the start of a long journey, but I'm excited by the research that this resource will allow us to do."
The new resource is described online today in the journal 'Cell'.