Alu RNA pseudoknot alterations influence SRP9/SRP14 association

There are over 1 million Alu elements in the human genome which can be transcribed into discrete, RNA polymerase III transcribed noncoding Alu RNAs. These Alu RNAs often interact with and are regulated by the protein heterodimer SRP9/SRP14. This interaction is dependent on a 5' pseudoknot domain in the Alu RNA that is thought to be held together by a canonical nucleotide triad within a U-turn motif. Herein, we discover a significant reduction in BC200 expression after mutation of a critical guanosine in the U-turn motif within its pseudoknot domain. We studied a recently discovered short human Alu RNA, EB120, which lacks the canonical Alu RNA U-turn nucleotide triad. We tested the expression of EB120 in 18 different human cell lines and tissues. EB120 was found to lack association with SRP9/SRP14 in a cellular context. Small-angle X-ray scattering followed by atomistic computation structure prediction suggests the BC200 Alu domain and its U-turn mutant both possess a canonical Alu RNA fold, while EB120 lacks one. Our results highlight the structural diversity of Alu RNA, and the impact mutations may have on Alu RNA function.

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Publication Details

Journal
RNA
Published
2025-05-09
DOI
https://doi.org/10.1261/rna.080359.124
Primary Topic
RNA and protein synthesis mechanisms
Type
article
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article

Alu RNA pseudoknot alterations influence SRP9/SRP14 association

Sean A. McKenna, Nancy Black, Markus Meier, Gay Pauline Padilla‐Meier et al.
RNA
RNA and protein synthesis mechanisms
article

Alu RNA pseudoknot alterations influence SRP9/SRP14 association

Sean A. McKenna, Nancy Black, Markus Meier, Gay Pauline Padilla‐Meier, Daniel Gussakovsky, Mira J.F. Brown, Jörg Stetefeld, Trushar R. Patel, Evan P. Booy, Higor Sette Pereira
article en

Abstract

There are over 1 million Alu elements in the human genome which can be transcribed into discrete, RNA polymerase III transcribed noncoding Alu RNAs. These Alu RNAs often interact with and are regulated by the protein heterodimer SRP9/SRP14. This interaction is dependent on a 5' pseudoknot domain in the Alu RNA that is thought to be held together by a canonical nucleotide triad within a U-turn motif. Herein, we discover a significant reduction in BC200 expression after mutation of a critical guanosine in the U-turn motif within its pseudoknot domain. We studied a recently discovered short human Alu RNA, EB120, which lacks the canonical Alu RNA U-turn nucleotide triad. We tested the expression of EB120 in 18 different human cell lines and tissues. EB120 was found to lack association with SRP9/SRP14 in a cellular context. Small-angle X-ray scattering followed by atomistic computation structure prediction suggests the BC200 Alu domain and its U-turn mutant both possess a canonical Alu RNA fold, while EB120 lacks one. Our results highlight the structural diversity of Alu RNA, and the impact mutations may have on Alu RNA function.

RNAVol. 31(8)
University of Lethbridge (CA), University of Manitoba (CA)
Openalex Percentile: Top 91%
RNA and protein synthesis mechanisms
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