Evidence map›Paper›PMID 35717998›Full record

ArticleJournal of molecular biology2022

Solution Structure of NPSL2, A Regulatory Element in the oncomiR-1 RNA.

Yaping Liu, Aldrex Munsayac, Ian Hall, Sarah C Keane

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Mechanisms underlining R-loop biology and implications for human disease.Frontiers in cell and developmental biology · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Enhanced TROSY Effect in [2-Angewandte Chemie (International ed. in English) · 2024
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Yaping LiuBiophysics Program, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA. Electronic address: https://twitter.com/YapingLiu5.
Aldrex MunsayacDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA.
Ian HallDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA. Electronic address: https://twitter.com/ihallu14.
Sarah C KeaneBiophysics Program, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA; Department of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109, USA. Electronic address: sckeane@umich.edu.
University of Michigan–Ann Arbor · US

Funding

The Biophysics Collaborative Access Team (User Training and Outreach)P30GM138395 · NIGMS · ILLINOIS INSTITUTE OF TECHNOLOGY · PI THOMAS C IRVING · 2021 to 2026
$16.5M
Michigan Chemistry-Biology Interface Training ProgramT32GM132046 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Emily E Scott, Wenjing Wang · 2019 to 2026
$4.1M
Biophysics of regulatory RNAs and RNPs - Equipment SupplementR35GM138279 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sarah Courtney Keane · 2020 to 2026
$2.6M
Advanced Pixel Array Detector for Time-Resolved SAXS and Fiber DiffractionS10OD018090 · OD · ILLINOIS INSTITUTE OF TECHNOLOGY · PI IRVING, THOMAS C · 2014 to 2014
$529k
NIGMS NIH HHS P30 GM138395NIGMS NIH HHS R35 GM138279NIGMS NIH HHS T32 GM132046NIH HHS S10 OD018090
6 · The paper itself

Abstract

The miR-17 ∼ 92a polycistron, also known as oncomiR-1, is commonly overexpressed in multiple cancers and has several oncogenic properties. OncomiR-1 encodes six constituent microRNAs (miRs), each enzymatically processed with different efficiencies. However, the structural mechanism that regulates this differential processing remains unclear. Chemical probing of oncomiR-1 revealed that the Drosha cleavage sites of pri-miR-92a are sequestered in a four-way junction. NPSL2, an independent stem loop element, is positioned just upstream of pri-miR-92a and sequesters a crucial part of the sequence that constitutes the basal helix of pri-miR-92a. Disruption of the NPSL2 hairpin structure could promote the formation of a pri-miR-92a structure that is primed for processing by Drosha. Thus, NPSL2 is predicted to function as a structural switch, regulating pri-miR-92a processing. Here, we determined the solution structure of NPSL2 using solution NMR spectroscopy. This is the first high-resolution structure of an oncomiR-1 element. NPSL2 adopts a hairpin structure with a large, but highly structured, apical and internal loops. The 10-bp apical loop contains a pH-sensitive A

Indexed as

CarcinogenesisMicroRNAsR-Loop StructuresRNA Processing, Post-TranscriptionalAdenosineHumansNuclear Magnetic Resonance, BiomolecularRibonuclease IIIRNA CleavageAdenosineDROSHA protein, humanMicroRNAsMIRN17 microRNA, humanRibonuclease IIImicroRNANMR spectroscopyRNA structureThermal denaturation

Identifiers

PMID35717998
PMCPMC9474619
OpenAlexW4282961722

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.