Publications - Published papers

Please find below publications of our group. Currently, we list 501 papers. Some of the publications are in collaboration with the group of Sonja Prohaska and are also listed in the publication list for her individual group. Access to published papers (access) is restricted to our local network and chosen collaborators. If you have problems accessing electronic information, please let us know:

©NOTICE: All papers are copyrighted by the authors; If you would like to use all or a portion of any paper, please contact the author.

Unorthodox mRNA start site to extend the highly structured leader of retrotransposon Tto1 mRNA increases transposition rate

Gudrun Böhmdorfer, Ivo L. Hofacker, Karin Garber, Srecko Jelenic, Viktoria Nizhynska, Hirohiko Hirochika, Peter F. Stadler, Andreas Bachmair

Download


PREPRINT 05-013:
[ Publishers's page ]  paperID

Status:


RNA 11: 1181-1191 (2005)

Abstract


Retroelement RNAs serve as templates for both translation and reverse transcription into extrachromosomal DNA. DNA copies may be inserted into the host genome to multiply element sequences. This transpositional activity of retroelements is usually restricted to specific conditions, particularly to conditions that impose stress onto the host organism. In this work, we examined how the mRNA initiation point, and features of primary and secondary structure, of tobacco retrotransposon Tto1 RNA influence its transpositional activity. We found that the Tto1 RNA most abundant in nonstressed cells is not a substrate for reverse transcription. It is poorly translated, and its 5´ end does not contain a region of redundancy with the most prominent 3´ end. In contrast, expression of an mRNA with the 5´ end extended by 28 nt allows translation and gives rise to transposition events in the heterologous host, Arabidopsis thaliana. In addition, the presence of extended hairpins and of two short open reading frames in the 5´ leader sequence of Tto1 mRNA suggests that translation does not involve ribosome scanning from the mRNA 5´ end to the translation initiation site.

Keywords


Arabidopsis thaliana, retrotransposon, short upstream reading frame, translation efficiency