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Updated: May 15, 2026

Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates
Published on: May 10, 2022
Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional target
Mohammad Shahidul Makki1, E Cristy Ruteshouser, Vicki Huff
1Department of Genetics, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Unit 1010, Houston, TX 77030, USA.
Abstract:
Wilms tumor gene WT1 encodes a zinc finger-containing transcription factor which is required for renal development. Mutations in WT1 are observed in 20% of Wilms tumors (a pediatric kidney cancer), but the in vivo WT1 targets and associated molecular pathways involved in the etiology of Wilms tumor are still elusive. To identify WT1 targets we performed genome-wide comprehensive expression profiling using Affymetrix Gene Chip Mouse Genome 430 2.0 Arrays, comparing E13.5 mouse kidneys in which Wt1 had been somatically ablated with littermate controls. We identified Usp18 as the most differentially expressed gene in mutant kidney. Using tetracycline inducible cells we demonstrated a repressive effect of WT1 on USP18 expression. Conversely, knockdown of WT1 led to the upregulation of Usp18. Furthermore, direct binding of WT1 to the Usp18 promoter was demonstrated by ChIP assay. Overexpression of USP18 in murine and human cell lines resulted in cell proliferation. Additionally, Usp18 upregulation was observed in a mouse model of Wilms tumor. Taken together our data demonstrate that Usp18 is a transcriptional target of WT1 and suggest that increased expression of USP18 following WT1 loss contributes to Wilms tumorigenesis.
Insights
Wilms tumor gene WT1 normally suppresses USP18. Loss of WT1 in kidney development leads to increased USP18, promoting Wilms tumor growth.
Area of Science:
- Molecular Biology
- Developmental Biology
- Oncology
Background:
- The Wilms tumor gene WT1 is crucial for kidney development.
- WT1 mutations are found in 20% of Wilms tumors, but its targets in tumorigenesis remain unclear.
Purpose of the Study:
- To identify in vivo WT1 targets and understand their role in Wilms tumor etiology.
- To investigate the relationship between WT1 and USP18 expression in kidney development and cancer.
Main Methods:
- Genome-wide expression profiling in mouse kidneys with Wt1 ablation.
- Analysis of USP18 regulation by WT1 using inducible cell lines.
- Chromatin immunoprecipitation (ChIP) assay to confirm WT1 binding to the Usp18 promoter.
Main Results:
- Usp18 was identified as the most differentially expressed gene upon Wt1 ablation.
- WT1 represses USP18 expression; WT1 knockdown upregulates Usp18.
- USP18 overexpression promotes cell proliferation, and Usp18 is upregulated in a Wilms tumor mouse model.
Conclusions:
- USP18 is a direct transcriptional target of WT1.
- Increased USP18 expression due to WT1 loss contributes to Wilms tumorigenesis.
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