14 October 2010

PiggyBac joins armoury in fight against cancer

Powerful mutation tool identifies new cancer genes

The PiggyBac transposon system was introduced into the mouse genome. This mouse line was engineered to possess its transposons (red) on chromosome 8. From there tranposons start jumping across the genome once activated by the transposase.

The PiggyBac transposon system was introduced into the mouse genome. This mouse line was engineered to possess its transposons (red) on chromosome 8. From there tranposons start jumping across the genome once activated by the transposase.

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Researchers have developed a genetic tool in mice to speed the discovery of novel genes involved in cancer. The system - called PiggyBac - has already been used by the team to identify novel candidate cancer-causing genes.

This new development of the PiggyBac system makes it a powerful addition to the armoury of genetic methods available to researchers for picking apart the genetic causes of cancer. It will complement advances in genomics and genetics of cancer, by providing biological validation to human mutations identified by cancer genome sequencing.

The PiggyBac process involves shipping cargos of genetic material - called transposons - around the genome using an engine known as a transposase. The team has incorporated the PiggyBac system into the mouse genome, where the transposons can jump from gene to gene, from chromosome to chromosome, disrupting or altering the activity of the genes where they land.

"Far from being destructive, this process is empowering our search for genes underlying cancer," says Professor Allan Bradley, from the Wellcome Trust Sanger Institute and senior author on the paper. "Some genes, when disrupted, will push cells along the road to tumour development. When we look at the tumours that develop in our mice, we can search for the molecular fingerprint of the transposons in the genome; this allows us to identify the disrupted genes that are the cause. But what is extraordinary about this new model is its adaptability - with PiggyBac, we can look at specific organs, we can switch genes on and switch genes off, we can look for cancer genes across the whole genome."

"It's the organism version of whole-genome study."

The team searched for novel cancer genes in 63 mouse blood cancers. The system opened new doors in the genome: when the researchers inspected 72 distinct locations at which their transposon had entered the genome, they found that a remarkable two-fifths of these genetic sites had never been detected before.

" What is extraordinary about this new model is its adaptability - with PiggyBac, we can look at specific organs, we can switch genes on and switch genes off, we can look for cancer genes across the whole genome. "

Professor Allan Bradley

"As well as highlighting the potential of this system to get at genetic regions previously beyond reach, the new genes that we have already identified using PiggyBac open exciting new avenues for future studies," says Dr Roland Rad, from the Wellcome Trust Sanger Institute and first author on the paper. "For instance, we found that one of the genes, called Spic, was disrupted in nine distinct myeloid leukaemia tumours in our mice. An event of this frequency merits study in human cancer and, when we take into account recent studies that have found this gene has a role in the development of white blood cells, we can be even more optimistic about the potential of this finding."

Other genes identified include Hdac7, which is known to participate in the creation of white blood cells in the thymus but has, to date, not been studied in the context of blood cancers; and Bcl9, a gene whose human equivalent is thought to be involved in leukaemia.

Researchers can now look in detail at the genetic equivalents in the human genome and ask what role their new genes play. One of the challenges of cancer genetics is that genomes in cancer cells can be ravaged by hundreds or even thousands of mutations. By looking at cancers modelled in the mouse, teams can begin to understand - at a biological level - which, among the thousands of mutations present, is the cause.

Before transposons researchers often used other methods, such as viruses, to cause mutations and generate tumours. Although these have had success in identifying genetic culprits in cancers of the blood and breast, they have not been effective in other cancer types.

It is only in recent years that researchers have been able to activate transposons to mutate genomes of higher organisms, such as mice - starting with a model called Sleeping Beauty. PiggyBac has many advantages over Sleeping Beauty and significantly extends the toolkit available to researchers. But the two systems can also complement one another.

"These transposons have particular preferences, particular ways of working," says Dr Pentao Liu, from the Wellcome Trust Sanger Institute and an author on the paper. "While Sleeping Beauty transposons slot into the genome most comfortably according to one pattern, PiggyBac follows another. So, naturally, one system will find genes that another might not. What is really exciting is that we have been able to incorporate both systems into our mouse lines so that they can be used together."

"By optimising PiggyBac in this way and by sharing these tools with researchers worldwide, we can hope to drive new discovery in cancer research."

The team have developed three types of transposons, which can be shipped around the genome to achieve different effects. Some will find genes involved in blood cancers, some in solid tumours, and some can find genes in both. They have also developed novel methods that let researchers activate the transposon only in the specific organ they are studying - be it lung, liver, pancreas or any other tissue in the mouse.

With the PiggyBac model now working to identify genes, the team will extend its reach - looking for further genes underlying a whole range of cancers in different organs of the mouse.

Notes to Editors

Publication details

  • PiggyBac transposon mutagenesis: a tool for cancer gene discovery in mice.

    Rad R, Rad L, Wang W, Cadinanos J, Vassiliou G, Rice S, Campos LS, Yusa K, Banerjee R, Li MA, de la Rosa J, Strong A, Lu D, Ellis P, Conte N, Yang FT, Liu P and Bradley A

    Science (New York, N.Y.) 2010;330;6007;1104-7

Funding

This work was supported by the Wellcome Trust and the German Research Foundation.

Participating Centres

  • The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
  • Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Spain

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The Wellcome Trust Sanger Institute, which receives the majority of its funding from the Wellcome Trust, was founded in 1992. The Institute is responsible for the completion of the sequence of approximately one-third of the human genome as well as genomes of model organisms and more than 90 pathogen genomes. In October 2006, new funding was awarded by the Wellcome Trust to exploit the wealth of genome data now available to answer important questions about health and disease.

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