Premature polyadenylation of MAGI3 is associated with diminished N⁶-methyladenosine in its large internal exon.

In cancer, tumor suppressor genes (TSGs) are frequently truncated, causing their encoded products to be non-functional or dominant-negative. We previously showed that premature polyadenylation (pPA) of MAGI3 truncates the gene, switching its functional role from a TSG to a dominant-negative oncogene. Here we report that MAGI3 undergoes pPA at the intron immediately downstream of its large internal exon, which is normally highly modified by N⁶-methyladenosine (m⁶A). In breast cancer cells that upregulate MAGI3 ^pPA , m⁶A levels in the large internal exon of MAGI3 are significantly reduced compared to cells that do not express MAGI3 ^pPA . We further find that MAGI3 ^pPA transcripts are significantly depleted of m⁶A modifications, in contrast to highly m⁶A-modified full-length MAGI3 mRNA. Finally, we analyze public expression data and find that other TSGs, including LATS1 and BRCA1, also undergo intronic pPA following large internal exons, and that m⁶A levels in these exons are reduced in pPA-activated breast cancer cells relative to untransformed mammary cells. Our study suggests that m⁶A may play a role in regulating intronic pPA of MAGI3 and possibly other TSGs, warranting further investigation.

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