Alternative Splicing Is a Major Factor Shaping Transcriptome Diversity in Mild and Severe COPD.

COPD Lung Diseases RNA Splicing Sequence Analysis

Journal

American journal of respiratory cell and molecular biology
ISSN: 1535-4989
Titre abrégé: Am J Respir Cell Mol Biol
Pays: United States
ID NLM: 8917225

Informations de publication

Date de publication:
05 Feb 2024
Historique:
medline: 5 2 2024
pubmed: 5 2 2024
entrez: 5 2 2024
Statut: aheadofprint

Résumé

The role of alternative splicing in Chronic Obstructive Pulmonary Disease (COPD) is still largely unknown. We aimed to investigate the differences in alternatively splicing events between patients with mild-to-moderate and severe COPD compared to non-COPD controls and to identify splicing factors associated with aberrant alternative splicing in COPD. For this purpose, we performed genome-wide RNA-seq analysis of bronchial brushings from 23 mild-to-moderate, 121 severe COPD patients, and 23 non-COPD controls. We found a significant difference in the frequency of alternative splicing events in mild-to-moderate and severe COPD compared to non-COPD controls. There were from 2x to 8x (depending on event type) more differential alternative splicing events in the severe than in the mild-to-moderate stage. The samples from severe COPD patients showed less intron retention and more exon skipping. Interestingly, the transcript levels of the top 10 differentially expressed splicing factors were significantly correlated with the percentage of many alternatively spliced transcripts in severe COPD. The aberrant alternative splicing in severe COPD was predicted to increase the overall protein-coding capacity of gene products. In conclusion, we observed large and significant differences in alternative splicing between bronchial samples of COPD and control individuals, with more events observed in severe than in mild-to-moderate COPD. The changes in the expression of several splicing factors correlated with prevalence of alternative splicing in severe COPD. Alternative splicing can indirectly impact gene expression by changing the relative abundance of protein-coding isoforms potentially influencing pathophysiological changes. The presented results provide a better understanding of COPD-related alternative splicing changes.

Identifiants

pubmed: 38315810
doi: 10.1165/rcmb.2023-0296OC
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Dmitry Khalenkow (D)

University Medical Centre Groningen, 10173, Department of Pulmonology and Pediatric Allergy, Groningen, Netherlands.
ERIBA, 548577, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

Corry-Anke Brandsma (CA)

University Medical Centre Groningen, 10173, Department of Pathology and Medical Biology, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

Wim Timens (W)

University Medical Centre Groningen, 10173, Department of Pathology and Medical Biology, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

David F Choy (DF)

Genentech Inc, 7412, South San Francisco, California, United States.

Michele A Grimbaldeston (MA)

Genentech Inc, 7412, South San Francisco, California, United States.

Carrie M Rosenberger (CM)

Genentech Inc, 7412, South San Francisco, California, United States.

Dirk-Jan Slebos (DJ)

University Medical Centre Groningen, 10173, Department of Pulmonary diseases, Groningen, Netherlands.

Huib A M Kerstjens (HAM)

University Medical Centre Groningen, 10173, Department of Pulmonology and Tuberculosis, Groningen, Netherlands.

Alen Faiz (A)

University of Technology Sydney, 1994, Respiratory Bioinformatics and Molecular Biology (RBMB), School of Life Sciences, Sydney, New South Wales, Australia.

Gerard H Koppelman (GH)

University Medical Centre Groningen, 10173, Department of Pulmonology and Pediatric Allergy, Beatrix Children's Hospital, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

Martijn C Nawijn (MC)

University Medical Centre Groningen, 10173, Lab allergology and pulmonary diseases, department of pathology and medical biology, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

Maarten van den Berge (M)

University Medical Centre Groningen, 10173, Department of Pulmonary Diseases, Groningen, Netherlands.
University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.

Victor Guryev (V)

University Medical Centre Groningen, Groningen Research Institute for Asthma and COPD, Groningen, Netherlands.
ERIBA, 548577, Groningen, Netherlands; v.guryev@umcg.nl.

Classifications MeSH