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Citation Arczewska KD, Tomazella GG, Lindvall JM, Kassahun H, Maglioni S, Torgovnick A, Henriksson J, Matilainen O, Marquis BJ, Nelson BC, Jaruga P, Babaie E, Holmberg CI, Burglin TR, Ventura N, Thiede B, Nilsen H. Active transcriptomic and proteomic reprogramming in the C. elegans nucleotide excision repair mutant xpa-1. Nucleic Acids Res, 2013.
PubMed ID 23580547
Short Description Active transcriptomic and proteomic reprogramming in the C. elegans nucleotide excision repair mutant xpa-1.
GEO Record: GSE39252 Platform: GPL200
Download gene-centric, log2 transformed data: WBPaper00042234.ce.mr.csv
# of Conditions 10
Full Description 1316625150_help Transcription-blocking oxidative DNA damage is believed to contribute to aging and to underlie activation of oxidative stress responses and down-regulation of insulin-like signaling (ILS) in Nucleotide Excision Repair (NER) deficient mice. Here, we present the first quantitative proteomic description of the Caenorhabditis elegans NER-defective xpa-1 mutant and compare the proteome and transcriptome signatures. Both methods indicated activation of oxidative stress responses, which was substantiated biochemically by a bioenergetic shift involving increased steady-state reactive oxygen species (ROS) and Adenosine triphosphate (ATP) levels. We identify the lesion-detection enzymes of Base Excision Repair (NTH-1) and global genome NER (XPC-1 and DDB-1) as upstream requirements for transcriptomic reprogramming as RNA-interference mediated depletion of these enzymes prevented up-regulation of genes over-expressed in the xpa-1 mutant. The transcription factors SKN-1 and SLR-2, but not DAF-16, were identified as effectors of reprogramming. As shown in human XPA cells, the levels of transcription-blocking 8,5'-cyclo-2'-deoxyadenosine lesions were reduced in the xpa-1 mutant compared to the wild type. Hence, accumulation of cyclopurines is unlikely to be sufficient for reprogramming. Instead, our data support a model where the lesion-detection enzymes NTH-1, XPC-1 and DDB-1 play active roles to generate a genomic stress signal sufficiently strong to result in transcriptomic reprogramming in the xpa-1 mutant.
Experimental Details:
WBPaper00042234:N2_rep1
WBPaper00042234:N2_rep2
WBPaper00042234:N2_rep3
WBPaper00042234:N2_rep4
WBPaper00042234:N2_rep5
WBPaper00042234:xpa-1_rep1
WBPaper00042234:xpa-1_rep2
WBPaper00042234:xpa-1_rep3
WBPaper00042234:xpa-1_rep4
WBPaper00042234:xpa-1_rep5.
Tags 1316625150_help
Method: microarray, Species: Caenorhabditis elegans, Topic: unclassified