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Research from the Batzer laboratory featured on the cover of PNAS



A paper from Dr. Batzer´s laboratory reporting the birth of a new gene in the primate lineage leading to humans is featured on the cover of the May 23rd, 2006 issue of PNAS. The paper describes the evolutionary history that led to the emergence of the chimeric SETMAR gene 40-58 million years ago, after the fusion between a preexisting gene and the coding region of a transposable element. The work not only provides insight into the conditions required for a successful gene fusion, but it also suggests a mechanism by which the circuitry underlying complex regulatory networks may be rapidly established.

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Cover Legend: The Philippine tarsier (Tarsius syrichta). Tarsiers belong to a primate lineage that lacks the chimeric SETMAR gene. The SETMAR gene arose 40-58 million years ago in the human primate lineage by the capture of the transposase gene from a selfish mobile element. Image courtesy of Katherine Gardner.

Abstract

The emergence of new genes and functions is of central importance to the evolution of species. The contribution of various types of duplications to genetic innovation has been extensively investigated. Less understood is the creation of new genes by recycling of coding material from selfish mobile genetic elements. To investigate this process, we reconstructed the evolutionary history of SETMAR, a new primate chimeric gene resulting from fusion of a SET histone methyltransferase gene to the transposase gene of a mobile element. We show that the transposase gene was recruited as part of SETMAR 40–58 million years ago, after the insertion of an Hsmar1 transposon downstream of a preexisting SET gene, followed by the de novo exonization of previously noncoding sequence and the creation of a new intron. The original structure of the fusion gene is conserved in all anthropoid lineages, but only the N-terminal half of the transposase is evolving under strong purifying selection. In vitro assays show that this region contains a DNA-binding domain that has preserved its ancestral binding specificity for a 19-bp motif located within the terminal-inverted repeats of Hsmar1 transposons and their derivatives. The presence of these transposons in the human genome constitutes a potential reservoir of ~1,500 perfect or nearly perfect SETMAR-binding sites. Our results not only provide insight into the conditions required for a successful gene fusion, but they also suggest a mechanism by which the circuitry underlying complex regulatory networks may be rapidly established.

Ref: Cordaux, R., S. Udit, M. A. Batzer and C. Feschotte (2006) Birth of a chimeric primate gene by capture of the transposase gene from a mobile element. Proceedings of the National Academy of Sciences of the USA 103: 8101-8106 ( pdf )

Other links: This Week In PNAS   Commentary by King Jordan

Additional information about research projects in the Batzer lab is available from the laboratory web site http://batzerlab.lsu.edu