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PMID: 41825960 Published · epublish English

Mutual feedback regulation between Poly(A)-specific ribonuclease (PARN) and cognate microRNAs.

Life science alliance ·Vol. 9 ·No. 5 ·2026-05-00

Kyritsis A, Beta RA, Scutelnic D, Stravokefalou V, Del Vescovo V, Arsenopoulou ZV, Papikinos K, Grasso M, Fontana F, Moutopoulou P, Tsiporis A, Samiotaki M, Panayotou G, Denti MA, Balatsos NA

Abstract

The majority of pri-miRNAs acquire a 5' cap and 3' poly(A) tail. Mature miRNAs recruit deadenylases that shorten poly(Α) tails triggering target mRNA degradation. Poly(A)-specific ribonuclease (PARN) is a deadenylase that also mediates late steps of noncoding RNA maturation. Herein, we show that PARN affects the expression of a subset of miRNAs in NCI-H520 cells of lung cancer origin, including miR-29a and miR-1207, which are also predicted to target PARN mRNA. PARN associates with pri-miR-29a and pri-miR-1207 regulating their poly(A) lengths. Conversely, miR-29a-3p and miR-1207-5p bind the 3' UTR of PARN mRNA and regulate its expression. Cleavage and polyadenylation specificity factor 6 (CPSF6) recruits PARN to pri-miRNAs and together they affect primary and mature miR-29a-3p levels. Modulation of PARN, miR-29a-3p, or miR-1207-5p expression affects cell migration. We present a model to describe the dynamic relation between PARN and miR-29a and discuss its biological significance.

Article Info
Journal
Life science alliance
Abbr.
Life Sci Alliance
ISSN
2575-1077
Published
2026-05-00
Language
English
Country/Region
United States
NLM ID
101728869
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