Multi-omics analysis identifies RFX7 targets involved in tumor suppression and neuronal processes

被引:6
|
作者
Schwab, Katjana [1 ]
Coronel, Luis [1 ]
Riege, Konstantin [1 ]
Sacramento, Erika K. [2 ]
Rahnis, Norman [2 ]
Haeckes, David [1 ]
Cirri, Emilio [2 ]
Groth, Marco [3 ]
Hoffmann, Steve [1 ]
Fischer, Martin [1 ]
机构
[1] Leibniz Inst Aging, Fritz Lipmann Inst FLI, Computat Biol Grp, Beutenbergstr 11, D-07745 Jena, Germany
[2] Leibniz Inst Aging, Fritz Lipmann Inst FLI, Core Facil Prote, Beutenbergstr 11, D-07745 Jena, Germany
[3] Leibniz Inst Aging, Fritz Lipmann Inst FLI, Core Facil Next Generat Sequencing, Beutenbergstr 11, D-07745 Jena, Germany
关键词
P53; PATHWAY; PROTEIN; PROGRESSION; VARIANTS; DREAM; LOCI; LINK; TP53;
D O I
10.1038/s41420-023-01378-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recurrently mutated in lymphoid neoplasms, the transcription factor RFX7 is emerging as a tumor suppressor. Previous reports suggested that RFX7 may also have a role in neurological and metabolic disorders. We recently reported that RFX7 responds to p53 signaling and cellular stress. Furthermore, we found RFX7 target genes to be dysregulated in numerous cancer types also beyond the hematological system. However, our understanding of RFX7's target gene network and its role in health and disease remains limited. Here, we generated RFX7 knock-out cells and employed a multi-omics approach integrating transcriptome, cistrome, and proteome data to obtain a more comprehensive picture of RFX7 targets. We identify novel target genes linked to RFX7's tumor suppressor function and underscoring its potential role in neurological disorders. Importantly, our data reveal RFX7 as a mechanistic link that enables the activation of these genes in response to p53 signaling.
引用
收藏
页数:9
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