AUF1 ligand circPCNX reduces cell proliferation by competing with p21 mRNA to increase p21 production

Mammalian circRNAs can influence different cellular processes by interacting with proteins and other nucleic acids. Here, we used ribonucleoprotein immunoprecipitation (RIP) analysis to identify systematically the circRNAs associated with the cancer-related protein AUF1. Among the circRNAs interacti...

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Vydáno v:	Nucleic acids research Ročník 49; číslo 3; s. 1631 - 1646
Hlavní autoři:	Tsitsipatis, Dimitrios, Grammatikakis, Ioannis, Driscoll, Riley K, Yang, Xiaoling, Abdelmohsen, Kotb, Harris, Sophia C, Yang, Jen-Hao, Herman, Allison B, Chang, Ming-Wen, Munk, Rachel, Martindale, Jennifer L, Mazan-Mamczarz, Krystyna, De, Supriyo, Lal, Ashish, Gorospe, Myriam
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	England Oxford University Press 22.02.2021
Témata:	3' Untranslated Regions Binding Sites Cell Proliferation - genetics Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis Cyclin-Dependent Kinase Inhibitor p21 - genetics Cyclin-Dependent Kinase Inhibitor p21 - metabolism HeLa Cells Heterogeneous Nuclear Ribonucleoprotein D0 - metabolism Humans RNA and RNA-protein complexes RNA, Circular - chemistry RNA, Circular - metabolism RNA, Messenger - metabolism
ISSN:	0305-1048, 1362-4962, 1362-4962
On-line přístup:	Získat plný text
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Shrnutí:	Mammalian circRNAs can influence different cellular processes by interacting with proteins and other nucleic acids. Here, we used ribonucleoprotein immunoprecipitation (RIP) analysis to identify systematically the circRNAs associated with the cancer-related protein AUF1. Among the circRNAs interacting with AUF1 in HeLa (human cervical carcinoma) cells, we focused on hsa_circ_0032434 (circPCNX), an abundant target of AUF1. Overexpression of circPCNX specifically interfered with the binding of AUF1 to p21 (CDKN1A) mRNA, thereby promoting p21 mRNA stability and elevating the production of p21, a major inhibitor of cell proliferation. Conversely, silencing circPCNX increased AUF1 binding to p21 mRNA, reducing p21 production and promoting cell division. Importantly, eliminating the AUF1-binding region of circPCNX abrogated the rise in p21 levels and rescued proliferation. Therefore, we propose that the interaction of circPCNX with AUF1 selectively prevents AUF1 binding to p21 mRNA, leading to enhanced p21 mRNA stability and p21 protein production, thereby suppressing cell growth.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0305-1048 1362-4962 1362-4962
DOI:	10.1093/nar/gkaa1246