Enhancers regulate genes linked to severe and mild childhood asthma.

Childhood asthma Enhancer Gene expression Gene regulation Peripheral blood leukocytes Severe asthma

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
30 Jul 2024
Historique:
received: 09 02 2023
revised: 03 07 2024
accepted: 09 07 2024
medline: 7 8 2024
pubmed: 7 8 2024
entrez: 7 8 2024
Statut: epublish

Résumé

Children with severe asthma suffer from recurrent symptoms and impaired quality of life despite advanced treatment. Underlying causes of severe asthma are not completely understood, although genetic mechanisms are known to be important. The aim of this study was to identify gene regulatory enhancers in leukocytes, to describe the role of these enhancers in regulating genes related to severe and mild asthma in children, and to identify known asthma-related SNPs situated in proximity to enhancers. Gene enhancers were identified and expression of enhancers and genes were measured by Cap Analysis Gene Expression (CAGE) data from peripheral blood leukocytes from children with severe asthma (n = 13), mild asthma (n = 15), and age-matched controls (n = 9). From a comprehensive set of 8,289 identified enhancers, we further defined a robust sub-set of the high-confidence and most highly expressed 4,738 enhancers. Known single nucleotide polymorphisms, SNPs, related to asthma coincided with enhancers in general as well as with specific enhancer-gene interactions. Blocks of enhancer clusters were associated with genes including TGF-beta, PPAR and IL-11 signaling as well as genes related to vitamin A and D metabolism. A signature of 91 enhancers distinguished between children with severe and mild asthma as well as controls. Gene regulatory enhancers were identified in leukocytes with potential roles related to severe and mild asthma in children. Enhancers hosting known SNPs give the opportunity to formulate mechanistic hypotheses about the functions of these SNPs.

Sections du résumé

Background UNASSIGNED
Children with severe asthma suffer from recurrent symptoms and impaired quality of life despite advanced treatment. Underlying causes of severe asthma are not completely understood, although genetic mechanisms are known to be important.
Objective UNASSIGNED
The aim of this study was to identify gene regulatory enhancers in leukocytes, to describe the role of these enhancers in regulating genes related to severe and mild asthma in children, and to identify known asthma-related SNPs situated in proximity to enhancers.
Methods UNASSIGNED
Gene enhancers were identified and expression of enhancers and genes were measured by Cap Analysis Gene Expression (CAGE) data from peripheral blood leukocytes from children with severe asthma (n = 13), mild asthma (n = 15), and age-matched controls (n = 9).
Results UNASSIGNED
From a comprehensive set of 8,289 identified enhancers, we further defined a robust sub-set of the high-confidence and most highly expressed 4,738 enhancers. Known single nucleotide polymorphisms, SNPs, related to asthma coincided with enhancers in general as well as with specific enhancer-gene interactions. Blocks of enhancer clusters were associated with genes including TGF-beta, PPAR and IL-11 signaling as well as genes related to vitamin A and D metabolism. A signature of 91 enhancers distinguished between children with severe and mild asthma as well as controls.
Conclusions UNASSIGNED
Gene regulatory enhancers were identified in leukocytes with potential roles related to severe and mild asthma in children. Enhancers hosting known SNPs give the opportunity to formulate mechanistic hypotheses about the functions of these SNPs.

Identifiants

pubmed: 39108895
doi: 10.1016/j.heliyon.2024.e34386
pii: S2405-8440(24)10417-3
pmc: PMC11301366
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e34386

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Tahmina Akhter (T)

Department of Biosciences and Nutrition, Karolinska Institutet, 141 83, Stockholm, Sweden.

Enrichetta Mileti (E)

Department of Biosciences and Nutrition, Karolinska Institutet, 141 83, Stockholm, Sweden.

Maura M Kere (MM)

Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, 118 83, Stockholm, Sweden.

Johan Kolmert (J)

Institute of Environmental Medicine, Karolinska Institutet, 171 77, Stockholm, Sweden.

Jon R Konradsen (JR)

Department of Women's and Children's Health, Karolinska Institutet, 171 77, Stockholm, Sweden.

Gunilla Hedlin (G)

Department of Women's and Children's Health, Karolinska Institutet, 171 77, Stockholm, Sweden.

Erik Melén (E)

Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, 118 83, Stockholm, Sweden.

Carsten O Daub (CO)

Department of Biosciences and Nutrition, Karolinska Institutet, 141 83, Stockholm, Sweden.
Science for Life Laboratory, Stockholm, Sweden.

Classifications MeSH