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KMID : 0624620230560090514
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BMB Reports
2023 Volume.56 No. 9 p.514 ~ p.519
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Intron retention decreases METTL3 expression by inhibiting mRNA export to the cytoplasm
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Lee Sang-Soo
Jung Hae-Soo
Choi Sun-Kyung
Cho Nam-Joon
Kim Eun-Mi
Kim Kee-Kwang
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Abstract
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Methyltransferase-like 3 (METTL3), a key component of the m6A methyltransferase complex, regulates the splicing, nuclear transport, stability, and translation of its target genes. However, the mechanism underlying the regulation of METTL3 expression by alternative splicing (AS) remains unknown. We analyzed the expression pattern of METTL3 after AS in human tissues and confirmed the expression of an isoform retaining introns 8 and 9 (METTL3-IR). We confirmed the different intracellular localizations of METTL3-IR and METTL3 proteins using immunofluorescence microscopy. Furthermore, the endogenous expression of METTL3-IR at the protein level was different from that at the mRNA level. We found that 3’-UTR generation by intron retention (IR) inhibited the export of METTL3-IR mRNA to the cytoplasm, which in turn suppressed protein expression. To the best of our knowledge, this is the first study to confirm the regulation of METTL3 gene expression by AS, providing evidence that the suppression of METTL3 protein expression by IR is an integral part of the mechanism by which 3’-UTR generation regulates protein expression via inhibition of RNA export to the cytoplasm.
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KEYWORD
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Alternative splicing, Gene expression, Intron retention, METTL3, mRNA export
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