7SHX
A functional SNP regulates E-cadherin expression by dynamically remodeling the 3D structure of a promoter-associated non-coding RNA transcript, NMR, minimized average structure
Summary for 7SHX
Entry DOI | 10.2210/pdb7shx/pdb |
NMR Information | BMRB: 51127 |
Descriptor | RNA (94-MER) (1 entity in total) |
Functional Keywords | parna, snp, rna |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 30487.21 |
Authors | Sharma, S.,Varani, G. (deposition date: 2021-10-11, release date: 2022-10-19, Last modification date: 2024-05-15) |
Primary citation | Sharma, S.,Pisignano, G.,Merulla, J.,Catapano, C.V.,Varani, G. A functional SNP regulates E-cadherin expression by dynamically remodeling the 3D structure of a promoter-associated non-coding RNA transcript. Nucleic Acids Res., 50:11331-11343, 2022 Cited by PubMed Abstract: Transcription of E-cadherin, a tumor suppressor that plays critical roles in cell adhesion and the epithelial-mesenchymal transition, is regulated by a promoter-associated non-coding RNA (paRNA). The sense-oriented paRNA (S-paRNA) includes a functional C/A single nucleotide polymorphism (SNP rs16260). The A-allele leads to decreased transcriptional activity and increased prostate cancer risk. The polymorphic site is known to affect binding of a microRNA-guided Argonaute 1 (AGO1) complex and recruitment of chromatin-modifying enzymes to silence the promoter. Yet the SNP is distant from the microRNA-AGO1 binding domain in both primary sequence and secondary structure, raising the question of how regulation occurs. Here we report the 3D NMR structure of the 104-nucleotide domain of the S-paRNA that encompasses the SNP and the microRNA-binding site. We show that the A to C change alters the locally dynamic and metastable structure of the S-paRNA, revealing how the single nucleotide mutation regulates the E-cadherin promoter through its effect on the non-coding RNA structure. PubMed: 36243981DOI: 10.1093/nar/gkac875 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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