Evidence map›Paper›PMID 38131377›Full record

ArticleJCI insight2023

Large-scale functional inference for skin-expressing lncRNAs using expression and sequence information.

Matthew T Patrick, Sutharzan Sreeskandarajan, Alanna Shefler, Rachael Wasikowski, Mrinal K Sarkar, Jiahan Chen, Tingting Qin, Allison C Billi, J Michelle Kahlenberg, Errol Prens and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

16 authors at 10 institutions in 5 countries.

Matthew T PatrickDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Sutharzan SreeskandarajanDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Alanna SheflerDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Rachael WasikowskiDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Mrinal K SarkarDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Jiahan ChenDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Tingting QinDepartment of Computational Medicine & Bioinformatics and.
Allison C BilliDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
J Michelle KahlenbergDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Errol PrensDepartment of Dermatology, Erasmus University Medical Center, Rotterdam, Netherlands.
Alain HovnanianLaboratory of Genetic Skin Diseases, Imagine Institute, Paris, France.
Stephan WeidingerDepartment of Dermatology and Allergy, University Medical Center Schleswig-Holstein, Kiel, Germany.
James T ElderDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Chao-Chung KuoInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University, Aachen, Germany.
Johann E GudjonssonDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Lam C TsoiDepartment of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Michigan Medicine · USUniversity of Michigan · USCincinnati Children's Hospital Medical Center · USErasmus MC · NLInstitut des Maladies Génétiques Imagine · FRInstitute of Bioinformatics · INNorth Carolina State University · USRWTH Aachen University · DEUniversity Hospital Schleswig-Holstein · DEVeterans Health Administration · US

Funding

Linkage analysis of familial psoriasis(Supplement)R01AR042742 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 1994 to 2021
$10.1M
University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDRZEJ A. DLUGOSZ · 2019 to 2026
$6.6M
Genetic and Genomic Dissection of Psoriatic ArthritisR01AR063611 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD, GLADMAN, DAFNA D · 2012 to 2023
$6.2M
Identification of Psoriatic Arthritis Genes in the MHCR01AR050511 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2004 to 2013
$4.2M
Immunogenomics and Systems Biology CoreUC2AR081033 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson, Lam Cheung Tsoi · 2022 to 2026
$3.3M
Combined Analysis of Gene Expression and DNA Variation in PsoriasisR01AR054966 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2007 to 2011
$3.2M
Functional Genomics of PsoriasisR01AR065183 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2013 to 2016
$1.7M
Mechanisms of sex discrepancy in autoimmune disease: Regulation of the female-biased VGLL3 immune pathwayK08AR078251 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BILLI, ALLISON CHELSA · 2021 to 2025
$865k
Integrative Biology Approach to Identify and Characterize Roles of lncRNAs Associated with Psoriasis PathologyK01AR072129 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TSOI, LAM CHEUNG · 2017 to 2021
$500k
NIAMS NIH HHS K01 AR072129NIAMS NIH HHS K08 AR078251NIAMS NIH HHS P30 AR075043NIAMS NIH HHS R01 AR042742NIAMS NIH HHS R01 AR050511NIAMS NIH HHS R01 AR054966NIAMS NIH HHS R01 AR063611NIAMS NIH HHS R01 AR065183NIAMS NIH HHS UC2 AR081033
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) regulate the expression of protein-coding genes and have been shown to play important roles in inflammatory skin diseases. However, we still have limited understanding of the functional impact of lncRNAs in skin, partly due to their tissue specificity and lower expression levels compared with protein-coding genes. We compiled a comprehensive list of 18,517 lncRNAs from different sources and studied their expression profiles in 834 RNA-Seq samples from multiple inflammatory skin conditions and cytokine-stimulated keratinocytes. Applying a balanced random forest to predict involvement in biological functions, we achieved a median AUROC of 0.79 in 10-fold cross-validation, identifying significant DNA binding domains (DBDs) for 39 lncRNAs. G18244, a skin-expressing lncRNA predicted for IL-4/IL-13 signaling in keratinocytes, was highly correlated in expression with F13A1, a protein-coding gene involved in macrophage regulation, and we further identified a significant DBD in F13A1 for G18244. Reflecting clinical implications, AC090198.1 (predicted for IL-17 pathway) and AC005332.6 (predicted for IFN-γ pathway) had significant negative correlation with the SCORAD metric for atopic dermatitis. We also utilized single-cell RNA and spatial sequencing data to validate cell type specificity. Our research demonstrates lncRNAs have important immunological roles and can help prioritize their impact on inflammatory skin diseases.

Indexed as

RNA, Long NoncodingSkin DiseasesHumansSkinRNA, Long NoncodingBioinformaticsDermatologyGeneticsGenetic variationSkin

Identifiers

PMID38131377
PMCPMC10807743
OpenAlexW4390046024

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.