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| Home > Publications database > Alternative mRNA Splicing Controls the Functions of the Histone H3K27 Demethylase UTX/KDM6A. |
| Home > Publications database > Alternative mRNA Splicing Controls the Functions of the Histone H3K27 Demethylase UTX/KDM6A. |
| Journal Article | DKFZ-2023-01300 |
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2023
MDPI
Basel
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Please use a persistent id in citations: doi:10.3390/cancers15123117
Abstract: The UTX/KDM6A histone H3K27 demethylase plays an important role in development and is frequently mutated in cancers such as urothelial cancer. Despite many studies on UTX proteins, variations in mRNA splicing have been overlooked. Using Nanopore sequencing, we present a comprehensive analysis of UTX/KDM6A splicing events in human cell lines and in tissue samples from bladder cancer cases and normal epithelia. We found that the central region of UTX mRNAs encoded by exons 12 to 17 undergoes extensive alternative splicing. Up to half of all stable mRNAs (8-48% in bladder tissues and 18-58% in cell lines) are represented by the UTX canonical isoform lacking exon 14 encoding a nuclear localization sequence, and hence exon 14-containing UTX isoforms exclusively localize to the nucleus, unlike the cytonuclear localization of the canonical isoform. Chromatin association was also higher for exon-14-containing isoforms compared to the canonical UTX. Using quantitative mass spectrometry, we found that all UTX isoforms integrated into the MLL3 and MLL4, PR-DUB and MiDAC complexes. Interestingly, one of the novel UTX isoforms, which lacks exons 14 and 16, fails to interact with PR-DUB and MiDAC complex members. In conclusion, UTX mRNAs undergo extensive alternative splicing, which controls the subcellular localization of UTX and its interactions with other chromatin regulatory complexes.
Keyword(s): alternative splicing ; bladder cancer ; cancer biology ; chromatin ; histone demethylase ; histone methylation ; proteomics
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