G-quadruplexes offer a conserved structural motif for NONO recruitment to NEAT1 architectural lncRNA

Author:

Simko Eric A J12ORCID,Liu Honghe12,Zhang Tao12,Velasquez Adan12,Teli Shraddha12,Haeusler Aaron R12,Wang Jiou12ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, 615 N. Wolfe St, Baltimore, MD 21205, USA

2. Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

Abstract

Abstract The long non-coding RNA NEAT1 serves as a scaffold for the assembly of paraspeckles, membraneless nuclear organelles involved in gene regulation. Paraspeckle assembly requires NEAT1 recruitment of the RNA-binding protein NONO, however the NEAT1 elements responsible for recruitment are unknown. Herein we present evidence that previously unrecognized structural features of NEAT1 serve an important role in these interactions. Led by the initial observation that NONO preferentially binds the G-quadruplex conformation of G-rich C9orf72 repeat RNA, we find that G-quadruplex motifs are abundant and conserved features of NEAT1. Furthermore, we determine that NONO binds NEAT1 G-quadruplexes with structural specificity and provide evidence that G-quadruplex motifs mediate NONO-NEAT1 association, with NONO binding sites on NEAT1 corresponding largely to G-quadruplex motifs, and treatment with a G-quadruplex-disrupting small molecule causing dissociation of native NONO-NEAT1 complexes. Together, these findings position G-quadruplexes as a primary candidate for the NONO-recruiting elements of NEAT1 and provide a framework for further investigation into the role of G-quadruplexes in paraspeckle formation and function.

Funder

National Institutes of Health

U.S. Department of Defense

Muscular Dystrophy Association

Robert Packard Center for ALS Research, Johns Hopkins University

Publisher

Oxford University Press (OUP)

Subject

Genetics

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