Their discoveries will be published in three milestone papers in the journal Nature Genetics.

The research was coordinated by the RIKEN Yokohama Omics Science Center in Japan as part of the FANTOM4 consortium, with researchers from The University of Queensland's Institute for Molecular Bioscience playing major roles in two of the papers.

PhD student Ryan Taft led one paper, on which Professor John Mattick was the senior author, while Associate Professor Sean Grimmond was a senior author on another paper led by Dr Geoff Faulkner.

"FANTOM4 has shown that instead of having one or a few 'master regulator' genes that control growth and development, there is a sophisticated network of regulatory elements that subtly influence the ways in which genes are expressed in different cells in the body," Professor John Mattick said.

This information will be very useful to medical and biological researchers, according to Associate Professor Sean Grimmond.

"We can use it to discover how cells transform from rapidly-growing 'blank slate' cells to mature cells with a specific function. This knowledge will help us determine, for example, why some cells turn cancerous, or how to control stem cells for use in regenerative medicine."

One of the papers describes the discovery of tiny RNAs, the smallest genetic elements yet known, which are linked to the expression of individual genes. Tiny RNAs are 18 nucleotides long, 100 times smaller than an average gene.

"Researchers had previously noticed small lengths of RNA in the genome, but thought that they were degraded segments of larger genetic elements," Mr Taft said.

"We found that they were too common and too specifically distributed to be rubbish. They are widely associated with promoters that switch on genes, and we believe they may have a role in gene activation. Once we understand their role more explicitly, we hope to use tiny RNAs to artificially control gene expression."

RNA is a molecule similar to DNA that translates the genetic information in DNA into proteins, or as in the case of tiny RNAs, can regulate longer RNA molecules before they are translated to proteins.

Another paper investigated retrotransposons, genetic elements that move around the genome and leave copies of themselves behind.

"The dogma in the field is that retrotransposons are only active in cancer cells and cells that turn into eggs and sperm," Dr Faulkner said. "Our results showed that retrotransposons that can no longer move around the genome may still be expressed in a broad range of cells, and thereby regulate the expression of nearby genes."

This is the fourth incarnation of the FANTOM consortium, which seeks to discover more about the workings of mammalian genomes through large-scale "systems biology" approaches.

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Journal References:

1. Faulkner et al. The regulated retrotransposon transcriptome of mammalian cells. Nature Genetics, 2009; DOI: 10.1038/ng.368
2. Suzuki et al. The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line. Nature Genetics, 2009; DOI: 10.1038/ng.375
3. Taft et al. Tiny RNAs associated with transcription start sites in animals. Nature Genetics, 2009; DOI: 10.1038/ng.312