Epithelial-specific histone modification of the miR-96/182 locus targeting AMAP1 mRNA predisposes p53 to suppress cell invasion in epithelial cells

Handa, Haruka; Hashimoto, Ari; Hashimoto, Shigeru; Sugino, Hirokazu; Oikawa, Tsukasa; Sabe, Hisataka

Epithelial-specific histone modification of the miR-96/182 locus targeting AMAP1 mRNA predisposes p53 to suppress cell invasion in epithelial cells

Handa, Haruka; Hashimoto, Ari; Hashimoto, Shigeru et al.

Cell communication and signaling, 2018, 16, 94

Permalink : https://hdl.handle.net/2115/72942

このアイテムのアクセス数:705件（2026-10-12 19:25 集計）

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01_Handa2018_Article_Epithelial-specificHistoneModi	pdf	2.71 MB	507
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論文情報

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アクセス権	open access
URI	https://hdl.handle.net/2115/72942
タイトル	Epithelial-specific histone modification of the miR-96/182 locus targeting AMAP1 mRNA predisposes p53 to suppress cell invasion in epithelial cells
著者	Handa, Haruka ; Hashimoto, Ari ; Hashimoto, Shigeru ; Sugino, Hirokazu ; Oikawa, Tsukasa ; Sabe, Hisataka
著者名 Handa, Haruka
e-Rad_Researcher 60390803 著者名 Hashimoto, Ari
e-Rad_Researcher 50311303 著者名 Hashimoto, Shigeru
著者名 Sugino, Hirokazu
e-Rad_Researcher 20457055 著者名 Oikawa, Tsukasa
e-Rad_Researcher 40187282 著者名 Sabe, Hisataka
言語	英語
キーワード	AMAP1
	miRNA
	miR-96/182
	p53
	Epithelial cell invasion
発行日	2018-12-04
出版者	BioMed Central
収録物名	Cell communication and signaling
巻(号)	16
ページ	94
抄録	Background: TP53 mutations in cancer cells often evoke cell invasiveness, whereas fibroblasts show invasiveness in the presence of intact TP53. AMAP1 (also called DDEF1 or ASAP1) is a downstream effector of ARF6 and is essential for the ARF6-driven cell-invasive phenotype. We found that AMAP1 levels are under the control of p53 (TP53 gene product) in epithelial cells but not in fibroblasts, and here addressed that molecular basis of the epithelial-specific function of p53 in suppressing invasiveness via targeting AMAP1. Methods: Using MDA-MB-231 cells expressing wild-type and p53 mutants, we identified miRNAs in which their expression is controlled by normal-p53. Among them, we identified miRNAs that target AMAP1 mRNA, and analyzed their expression levels and epigenetic statuses in epithelial cells and nonepithelial cells. Results: We found that normal-p53 suppresses AMAP1 mRNA in cancer cells and normal epithelial cells, and that more than 30 miRNAs are induced by normal-p53. Among them, miR-96 and miR-182 were found to target the 3′-untranslated region of AMAP1 mRNA. Fibroblasts did not express these miRNAs at detectable levels. The ENCODE dataset demonstrated that the promoter region of the miR-183-96-182 cistron is enriched with H3K27 acetylation in epithelial cells, whereas this locus is enriched with H3K27 trimethylation in fibroblasts and other non-epithelial cells. miRNAs, such as miR-423, which are under the control of p53 but not associated with AMAP1 mRNA, demonstrated similar histone modifications at their gene loci in epithelial cells and fibroblasts, and were expressed in these cells. Conclusion: Histone modifications of certain miRNA loci, such as the miR-183-96-182 cistron, are different between epithelial cells and non-epithelial cells. Such epithelial-specific miRNA regulation appears to provide the molecular basis for the epithelial-specific function of p53 in suppressing ARF6-driven invasiveness.
資源タイプ	学術雑誌論文
出版タイプ	Version of Record
権利情報	Creative Commons Attribution 4.0 International
PISSN	1478-811X
関連情報 (isIdenticalTo)	出版社版DOI https://doi.org/10.1186/s12964-018-0302-6