Evidence map›Paper›PMID 27009487›Full record

ArticleGenes and immunity2016

Alternative splicing directs two IL-20R2 isoforms and is responsible for the incomplete gene knockout via the exon I ablation.

H Zhou, X Liu, R Yu, T Long, R Zhao, H Liu, Y Xu, J G Liang, P Liang

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Alternative splicing and cancer: a systematic review.Signal transduction and targeted therapy · 2021
    Pooled it
  2. Alternative splicing isoforms in health and disease.Pflugers Archiv : European journal of physiology · 2018
    Review
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

9 authors at 3 institutions in 2 countries.

H ZhouDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
X LiuDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
R YuDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
T LongDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
R ZhaoDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
H LiuDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
Y XuDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
J G LiangClover Biopharmaceuticals, Chengdu, China.
P LiangDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Sichuan University, Chengdu, China.
Sichuan University · CNChengdu University · CNClover Biopharmaceuticals (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two heterodimeric receptors consisting of interleukin (IL)-20R2 are shared by three of the IL-20 family of cytokines, IL-19, IL-20 and IL-24. Along with IL-22, these cytokines are downstream effectors of IL-23 and have been implicated in keratinocyte functions and the pathogenesis of psoriasis. Surprisingly, whereas knocking out either the IL-23 or IL-22 gene abolished imiquimod-induced psoriatic phenotypes in mice, similar attempt for IL-20R2 had little effect. Here, we report that the apparent disparity may result from a new IL-20R2 isoform encoded by an alternatively spliced transcript which survived the previous attempt for IL-20R2 gene knockout via the exon I deletion.

Indexed as

Alternative SplicingAnimalsExonsGene DeletionInterleukin-22Interleukin-23InterleukinsMiceMice, Inbred BALB CMice, Inbred C57BLProtein IsoformsReceptors, Interleukininterleukin-20 receptorInterleukin-22Interleukin-23InterleukinsProtein IsoformsReceptors, Interleukin

Identifiers

PMID27009487
OpenAlexW2311666036

What Socratic holds

Textmetadata
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 Socratic graph.