They can be found in plants, animals and even in humans - inactive remains of jumping genes, transposons. Researchers are striving to develop active transposons from these remains, using them as tools to decode gene function.
At the Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch, Germany, researchers have now succeeded in reconstructing the first active transposon of the Harbinger transposon superfamily.
In the laboratory, the artificial transposon developed by Dr. Ludivine Sinzelle, Dr. Zsuzsanna Izsvák, and Dr. Zoltán Ivics also shows cut-and-paste transposition in human cells and promises to serve as a useful experimental system for investigating human gene function.
Transposons comprise about half of the human genome. "They are molecular parasites, similar to fleas, only that they are in the genome of the host and not on its back," Dr. Zoltán Ivics explained. They jump, move, and proliferate through the host, without whom they could not survive. In most cases, transposons do not fulfill any function in the human genome. "However, not all are superfluous," Dr. Ivics went on to say. "More than 100 active genes, including some associated with the immune system, have been recognized as probably derived from transposons."
To reconstruct an active transposon, Dr. Ivics' team compared the DNA of various inactive Harbinger transposons, one of the largest superfamilies of transposons. Based on these results, they developed an artificial jumping gene. "We were very lucky," Dr. Ivics said. "The very first experiment was successful."
Moreover, in the course of evolution, transposons have been responsible for the emergence of new genes. Thus, through computerized gene analysis, Dr. Ivics' research team has discovered two new elements related to the Harbinger transposon. In a new project, Dr. Ivics aims to elucidate just what role these play in the human body.
Over the long term, scientists hope to use such transposons in gene therapy as well. With the aid of a transposon, an intact copy of a gene could be incorporated into the genome of a patient to repair a defective gene. "But until this can happen, there is still a lot to be done," Dr. Ivics pointed out. "The new gene should not just jump in anywhere."
*Transposition of a Reconstructed Harbinger Element in Human Cells and Functional Homology with Two Transposon-derived Cellular Genes
Ludivine Sinzelle1, Vladimir V. Kapitonov,2, Dawid P. Grzela1, Tobias Jursch1, Jerzy Jurka2, Zsuzsanna Izsvák1,3 and Zoltán Ivics11Max Delbrück Center for Molecular Medicine, Berlin, Germany;
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