Aryl Sulfonamides Degrade RBM39 and RBM23 by Recruitment to CRL4-DCAF15
Tabitha C. Ting,
Maria Goralski,
Katherine Klein,
Baiyun Wang,
Jiwoong Kim,
Yang Xie,
Deepak Nijhawan
Affiliations
Tabitha C. Ting
Medical Scientist Training Program, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Maria Goralski
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Katherine Klein
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Baiyun Wang
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Jiwoong Kim
Quantitative Biomedical Research Center, Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Yang Xie
Quantitative Biomedical Research Center, Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Deepak Nijhawan
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Corresponding author
Summary: Indisulam and related sulfonamides recruit the splicing factor RBM39 to the CRL4-DCAF15 E3 ubiquitin ligase, resulting in RBM39 ubiquitination and degradation. Here, we used a combination of domain mapping and random mutagenesis to identify domains or residues that are necessary for indisulam-dependent RBM39 ubiquitination. DCAF15 mutations at Q232 or D475 prevent RBM39 recruitment by indisulam. RBM39 is recruited to DCAF15 by its RRM2 (RNA recognition motif 2) and is ubiquitinated on its N terminus. RBM23, which is an RBM39 paralog, is also recruited to the CRL4-DCAF15 ligase through its RRM2 domain and undergoes sulfonamide-dependent degradation. Indisulam alters the expression of more than 3,000 genes and causes widespread intron retention and exon skipping. All of these changes can be attributed to RBM39, and none are the consequence of RBM23 degradation. Our findings demonstrate that indisulam selectively degrades RBM23 and RBM39, the latter of which is critically important for splicing and gene expression. : Ting et. al. demonstrate that indisulam and related sulfonamides recruit either RBM39 or RBM23 to the CRL4-DCAF15 ubiquitin ligase, leading to polyubiquitination and proteasomal degradation. Gene expression changes and splicing abnormalities resulting from indisulam treatment are the consequence of RBM39 degradation and not the result of RBM23 degradation. Keywords: DCAF15, RBM39, RBM23, CRL4, sulfonamides
