Regulatory networks revealed by transcriptional profiling of damaged Saccharomyces cerevisiae cells:: Rpn4 links base excision repair with proteasomes
Regulatory networks revealed by transcriptional profiling of damaged Saccharomyces cerevisiae cells:: Rpn4 links base excision repair with proteasomes
复制标题
DOI:
10.1128/mcb.20.21.8157-8167.2000
复制
发表时间:
2000-11-01
影响因子:
5.3
通讯作者:
Samson, LD
中科院分区:
文献类型:
--
作者:
Jelinsky, SA;Estep, P;Samson, LD
Exposure to carcinogenic alkylating agents, oxidizing agents, and ionizing radiation modulates transcript levels for over one third of Saccharomyces cerevisiae's 6,200 genes. Computational analysis delineates groups of coregulated genes whose upstream regions bear known and novel regulatory sequence motifs, One group of coregulated genes contain a number of DNA excision repair genes (including the MAG1 3-methyladenine DNA glycosylase gene) and a large selection of protein degradation genes. Moreover, transcription of these genes is modulated by the proteasome-associated protein Rpn4, most likely via its binding to MAGI upstream repressor sequence 2-like elements, that turn out to be almost identical to the recently identified proteasome-associated control element (G. Mannhaupt, R. Schnall, V. Karpov, I. Vetter, and H. Feldmann, FEES Lett. 450:27-34, 1999). We have identified a large number of genes whose transcription is influenced by Rpn4p.