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Multiple copies of the same "jumping genes" have been found in a salamander-infecting fungus.
Transposons, or jumping genes, can "copy and paste" themselves and have an effect on the organism. The majority of organisms have some repetitive DNA, some of which are jumping genes, but this can be detrimental and there are methods to stop or restrict this. However, the new study - led by the MRC Centre for Medical Mycology at the University of Exeter - finds a possible evolutionary advantage of these jumping genes in a fungus called Batrachochytrium salamandrivorans (Bsal). Not only did they find different versions of these jumping genes repeated multiple times in Bsal's genome - but the gene in question appears to have duplicated another group of genes that play a role in how severely it affects infected fire salamanders. "Bsal and related fungal species infect amphibians worldwide, and have been responsible for more than 90 extinctions," said first author Theresa Wacker. "Bsal infects the skin of salamanders and newts and causes severe wounds. "It emerged in Asia, where many newts and salamanders have some tolerance, but it has spread to Europe and is causing European salamander populations to decline. "Using new sequencing technologies, we found that Bsal has undergone a genome expansion compared to related species - that is to say, it now has a bigger genome with more genes and also more of these 'jumping gene' transposons." The new study found the ability of jumping gene transposons to copy and paste themselves contributed significantly to this expansion. "If you think of an organism's genome as a blueprint, transposons are like having many identical pages," Wacker explained. "And sometimes, during the process of copying and pasting, other parts of the book are also copied." It appears that this copying and pasting caused by repetitive jumping gene transposons has also amplified some skin-destroying genes. Having more of these skin-destruction genes allows the fungus to destroy the skin of salamanders more quickly, making it more deadly." Senior author Dr Rhys Farrer said repetitive DNA, including jumping genes, is sometimes referred to as "junk" DNA. "Most organisms have a few jumping gene transposons," he said. "In humans, they typically make up less than 1 per cent of the genome, and we have control mechanisms to prevent this from rising. "In Bsal, repeated jumping genes make up about 19 per cent of the genome. "Transposon jumping genes can interfere with regular gene function and cause problems for the organism - but for Bsal this seems to be outweighed by the advantages." The team are now doing further research. Dr Farrer said: "This kind of gene repetition is probably more widespread in nature than we currently realise. "If, as appears to be the case, it confers an evolutionary advantage for the pathogen by making it more virulent, it's not clear why this isn't much more common." The study's finding shed new light on the evolution of a major amphibian disease, and Dr Farrer called it a "paradigm shift" in terms of identifying repetitive genome content as a driving force behind its pathobiology. (ANI)
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