Evidence map›Paper›PMID 29066300›Full record

ArticleGene2018

Upregulation of functional Kv11.1a isoform expression by modified U1 small nuclear RNA.

Qiuming Gong, Matthew R Stump, Zhengfeng Zhou

Abstract read
In one paragraph

Article in Gene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

3 authors at 2 institutions in 1 country.

Qiuming GongKnight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, United States.
Matthew R StumpDepartment of Biology, George Fox University, Newberg, OR, United States.
Zhengfeng ZhouKnight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, United States. Electronic address: zhouzh@ohsu.edu.
Oregon Health & Science University · USGeorge Fox University · US

Funding

Pathogenesis of HERG Mutations in Human Long QT SyndromeR01HL068854 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ZHOU, ZHENGFENG · 2002 to 2018
$5.7M
NHLBI NIH HHS R01 HL068854
6 · The paper itself

Abstract

The KCNH2 or human ether-a go-go-related gene (hERG) encodes the Kv11.1 potassium channel that conducts the rapidly activating delayed rectifier potassium current in the heart. The expression of Kv11.1 C-terminal isoforms is directed by the alternative splicing and polyadenylation of intron 9. Splicing of intron 9 leads to the formation of a functional, full-length Kv11.1a isoform and polyadenylation of intron 9 results in the production of a non-functional, C-terminally truncated Kv11.1a-USO isoform. The relative expression of Kv11.1a and Kv11.1a-USO plays an important role in regulating Kv11.1 channel function. In the heart, only one-third of KCNH2 pre-mRNA is processed to Kv11.1a due to the weak 5' splice site of intron 9. We previously showed that the weak 5' splice site is caused by sequence deviation from the consensus, and that mutations toward the consensus sequence increased the efficiency of intron 9 splicing. It is well established that 5' splice sites are recognized by complementary base-paring with U1 small nuclear RNA (U1 snRNA). In this study, we modified the sequence of U1 snRNA to increase its complementarity to the 5' splice site of KCNH2 intron 9 and observed a significant increase in the efficiency of intron 9 splicing. RNase protection assay and western blot analysis showed that modified U1 snRNA increased the expression of the functional Kv11.1a isoform and concomitantly decreased the expression of the non-functional Kv11.1a-USO isoform. In patch-clamp experiments, modified U1 snRNA significantly increased Kv11.1 current. Our findings suggest that relative expression of Kv11.1 C-terminal isoforms can be regulated by modified U1 snRNA.

Indexed as

Alternative SplicingCell LineERG1 Potassium ChannelHEK293 CellsHumansIntronsPolyadenylationProtein IsoformsRNA PrecursorsRNA, Small NuclearRNA Splice SitesUp-RegulationERG1 Potassium ChannelKCNH2 protein, humanProtein IsoformsRNA PrecursorsRNA, Small NuclearRNA Splice SitesU1 small nuclear RNAAlternative polyadenylationArrhythmiahERGLong QT syndromeSplicingU1 snRNA

Identifiers

PMID29066300
PMCPMC5755592
OpenAlexW2766420668

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.