Analysis of Alternative mRNA Splicing in Vemurafenib-Resistant Melanoma Cells

Show full item record



Permalink

http://hdl.handle.net/10138/346421

Citation

Bokharaie, H.; Kolch, W.; Krstic, A. Analysis of Alternative mRNA Splicing in Vemurafenib-Resistant Melanoma Cells. Biomolecules 2022, 12, 993.

Title: Analysis of Alternative mRNA Splicing in Vemurafenib-Resistant Melanoma Cells
Author: Bokharaie, Honey; Kolch, Walter; Krstic, Aleksandar
Publisher: Multidisciplinary Digital Publishing Institute
Date: 2022-07-17
URI: http://hdl.handle.net/10138/346421
Abstract: Alternative mRNA splicing is common in cancers. In BRAF V600E-mutated malignant melanoma, a frequent mechanism of acquired resistance to BRAF inhibitors involves alternative splicing (AS) of BRAF. The resulting shortened BRAF protein constitutively dimerizes and conveys drug resistance. Here, we have analysed AS in SK-MEL-239 melanoma cells and a BRAF inhibitor (vemurafenib)-resistant derivative that expresses an AS, shortened BRAF V600E transcript. Transcriptome analysis showed differential expression of spliceosome components between the two cell lines. As there is no consensus approach to analysing AS events, we used and compared four common AS softwares based on different principles, DEXSeq, rMATS, ASpli, and LeafCutter. Two of them correctly identified the BRAF V600E AS in the vemurafenib-resistant cells. Only 12 AS events were identified by all four softwares. Testing the AS predictions experimentally showed that these overlapping predictions are highly accurate. Interestingly, they identified AS caused alterations in the expression of melanin synthesis and cell migration genes in the vemurafenib-resistant cells. This analysis shows that combining different AS analysis approaches produces reliable results and meaningful, biologically testable hypotheses.


Files in this item

Total number of downloads: Loading...

Files Size Format View
biomolecules-12-00993-v2.pdf 2.780Mb PDF View/Open

This item appears in the following Collection(s)

Show full item record