%0 Journal Article
%T Creation of a novel telomere-cutting endonuclease based on the EN domain of telomere-specific non-long terminal repeat retrotransposon, TRAS1
%A Kazutoshi Yoshitake
%A Hideyuki Aoyagi
%A Haruhiko Fujiwara
%J Mobile DNA
%D 2010
%I BioMed Central
%R 10.1186/1759-8753-1-13
%X Here, we created novel chimeric endonucleases to cut telomeres by fusing the endonuclease domain (TRAS1EN) of the silkworm's telomere specific non-long terminal repeat retrotransposon TRAS1 to the human telomere-binding protein, TRF1. An in vitro assay demonstrated that the TRAS1EN-TRF1 chimeric endonucleases (T-EN and EN-T) cut the human (TTAGGG)n repeats specifically. The concentration of TRAS1EN-TRF1 chimeric endonucleases necessary for the cleavage of (TTAGGG)n repeats was about 40-fold lower than that of TRAS1EN alone. When TRAS1EN-TRF1 endonucleases were introduced into human U2OS cancer cells using adenovirus vectors, the enzymes localized at telomeres of nuclei, cleaved and shortened the telomeric DNA by double-strand breaks. When human U2OS and HFL-1 fibroblast cells were infected with EN-T recombinant adenovirus, their cellular proliferation was suppressed for about 2 weeks after infection. In contrast, the TRAS1EN mutant (H258A) chimeric endonuclease fused with TRF1 (ENmut-T) did not show the suppression effect. The EN-T recombinant adenovirus induced telomere shortening in U2OS cells, activated the p53-dependent pathway and caused the senescence associated cellular responses, while the ENmut-T construct did not show such effects.A novel TRAS1EN-TRF1 chimeric endonuclease (EN-T) cuts the human telomeric repeats (TTAGGG)n specifically in vitro and in vivo. Thus, the chimeric endonuclease which is expressed from an adenoviral vector can suppress cell proliferation of cancer cells.Telomeres are specialized structures that protect chromosomal ends from gene erosion at cell divisions, nonhomologous chromosomal end joining and nuclease attack [1]. The DNA component of telomeres, typically 5-8 kb long, consists of tandem arrays of short, repetitive G-rich sequences--TTAGGG in vertebrates--oriented 5'- to -3' towards the end of the chromosome [2]. Each replication of human nuclear DNA results in a 50-200 base pair loss of the telomere. After reaching a critical s
%U http://www.mobilednajournal.com/content/1/1/13