A medical breakthrough which may help bring new insights on how genes are activated is being reported by scientists.
A medical breakthrough which may help bring new insights on how genes are activated is being reported by scientists. Roughly 3 metres of DNA is tightly folded into the nucleus of every cell in our body. This folding allows some genes to be 'expressed', or activated, while excluding others.
Dr Tim Mercer and Professor John Mattick from Sydney's Garvan Institute of Medical Research and Professor John Stamatoyannopoulos from Seattle's University of Washington analysed the genome's 3D structure, at high resolution.
Genes are made up of 'exons' and 'introns' - the former being the sequences that code for protein and are expressed, and the latter being stretches of noncoding DNA in-between.
As the genes are copied, or 'transcribed', from DNA into RNA, the intron sequences are cut or 'spliced' out and the remaining exons are strung together to form a sequence that encodes a protein. Depending on which exons are strung together, the same gene can generate different proteins.
Using vast amounts of data from the ENCODE project, Dr Tim Mercer and colleagues have inferred the folding of the genome, finding that even within a gene, selected exons are easily exposed.
Mercer said that imagine a long and immensely convoluted grape vine, its twisted branches presenting some grapes to be plucked easily, while concealing others beyond reach.
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Mercer asserted that their study has provides the first indication that the three-dimensional structure of the genome can influence the splicing of genes.
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Their findings have been published online in Nature Genetics.
Source-ANI