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嗜热四膜虫中RAD51表达的转录调控。

Transcriptional control of RAD51 expression in the ciliate Tetrahymena thermophila.

作者信息

Smith Joshua J, Cole Eric S, Romero Daniel P

机构信息

Department of Pharmacology, Medical School, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Nucleic Acids Res. 2004 Aug 10;32(14):4313-21. doi: 10.1093/nar/gkh771. Print 2004.

Abstract

The expression of Rad51p, a DNA repair protein that mediates homologous recombination, is induced by DNA damage and during both meiosis and exconjugant development in the ciliate Tetrahymena thermophila. To completely investigate the transcriptional regulation of Tetrahymena RAD51 expression, reporter genes consisting of the RAD51 5' non-translated sequence (5' NTS) positioned upstream of either the firefly luciferase or green fluorescent protein coding sequences have been targeted for recombination at the macronuclear btu1-1 (K350M) locus of T. thermophila strain CU522. Expression from RAD51-luciferase reporter constructs has been directly quantified from transformant whole cell lysates. Luciferase is induced to maximum levels in transformants harboring the full-length RAD51-luciferase reporter gene following exposure to DNA damaging UV irradiation. A series of truncations, deletions, insertions, substitutions and inversions of the RAD51 5' NTS have led to the identification of three distinct transcriptional promoter elements. The first of these sequence elements is required for basal levels of transcription. The second modulates expression in the absence of DNA damage, whereas the third ensures increased RAD51 transcription in response to DNA damage and during meiosis. Tetrahymena RAD51 is tightly regulated through these transcriptional elements to produce the appropriate expression during conjugation, and in response to DNA damage.

摘要

Rad51p是一种介导同源重组的DNA修复蛋白,其表达在嗜热四膜虫的DNA损伤时以及减数分裂和接合后发育过程中被诱导。为了全面研究嗜热四膜虫RAD51表达的转录调控,已将由位于萤火虫荧光素酶或绿色荧光蛋白编码序列上游的RAD51 5'非翻译序列(5' NTS)组成的报告基因靶向到嗜热四膜虫菌株CU522的大核btu1-1(K350M)位点进行重组。已从转化体全细胞裂解物中直接定量RAD51-荧光素酶报告构建体的表达。在暴露于DNA损伤性紫外线照射后,在携带全长RAD51-荧光素酶报告基因的转化体中,荧光素酶被诱导至最高水平。RAD51 5' NTS的一系列截断、缺失、插入、替换和倒位导致鉴定出三个不同的转录启动子元件。这些序列元件中的第一个是基础转录水平所必需的。第二个元件在没有DNA损伤的情况下调节表达,而第三个元件确保在DNA损伤时以及减数分裂期间RAD51转录增加。嗜热四膜虫RAD51通过这些转录元件受到严格调控,以在接合过程中以及对DNA损伤作出反应时产生适当的表达。

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