X-Irradiation Activates the Drosophila 1731 Retrotransposon LTR and Stimulates Secretion of an Extracellular Factor That Induces the 1731-LTR Transcription in Nonirradiated Cells.
スポンサーリンク
概要
- 論文の詳細を見る
Using constructs expressing the reporter gene under the control of the entire or deleted long terminal repeats (LTRs) of 1731, a Drosophila melanogaster retrotransposable element, we show that 1731-LTR is activated by X-irradiation in a dose- and time-dependent manner, and that a sequence located in the U3 region of these LTRs is required. The cis-acting element conferring X-responsiveness shows similarities to kappaB (κB)-like binding sequence. In response to X-irradiation, S2 Drosophila cells produced an extracellular factor which activates the 1731-LTR in nonirradiated cells. This factor was detected both when transfected cells were cocultured with inducing cells and when a conditioned medium taken from irradiated cultures was added.
- 社団法人 日本生化学会の論文
著者
-
Best-belpomme Martin
Iua Cnrs 1135 Universite P. Et M. Curie
-
Faure Eric
Ecologie Et Biologie Evolutive Institut De Chimie Biologique Universite De Provence
-
Champion Serge
Cnrs 1924 Faculte Des Pharmaciens
-
Best-Belpomme Martin
IUA CNRS 1135, Université P. et M. Curie
関連論文
- X-Irradiation Activates the Drosophila 1731 Retrotransposon LTR and Stimulates Secretio of an Extracellular Factor That Induces the 1731-LTR Transcription in Nonirradiated Cells
- X-Irradiation Activates the Drosophila 1731 Retrotransposon LTR and Stimulates Secretion of an Extracellular Factor That Induces the 1731-LTR Transcription in Nonirradiated Cells.