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Alternative Splicing Is a Major Factor Shaping Transcriptome Diversity in Mild and Severe Chronic Obstructive Pulmonary Disease.
Khalenkow, Dmitry; Brandsma, Corry-Anke; Timens, Wim; Choy, David F; Grimbaldeston, Michele A; Rosenberger, Carrie M; Slebos, Dirk-Jan; Kerstjens, Huib A M; Faiz, Alen; Koppelman, Gerard H; Nawijn, Martijn C; van den Berge, Maarten; Guryev, Victor.
Afiliação
  • Khalenkow D; European Research Institute for the Biology of Ageing.
  • Brandsma CA; Groningen Research Institute for Asthma and COPD.
  • Timens W; Department of Pediatric Pulmonology and Pediatric Allergology, Beatrix Children's Hospital.
  • Choy DF; Groningen Research Institute for Asthma and COPD.
  • Grimbaldeston MA; Department of Pathology and Medical Biology.
  • Rosenberger CM; Groningen Research Institute for Asthma and COPD.
  • Slebos DJ; Department of Pathology and Medical Biology.
  • Kerstjens HAM; Genentech, Inc., South San Francisco, California; and.
  • Faiz A; Genentech, Inc., South San Francisco, California; and.
  • Koppelman GH; Genentech, Inc., South San Francisco, California; and.
  • Nawijn MC; Department of Pulmonary Diseases, and.
  • van den Berge M; Department of Pulmonology and Tuberculosis, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Guryev V; Faculty of Science, Centre for Inflammation, Centenary Institute and University of Technology Sydney, Sydney, Australia.
Am J Respir Cell Mol Biol ; 70(5): 414-423, 2024 May.
Article em En | MEDLINE | ID: mdl-38315810
ABSTRACT
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 with non-COPD control subjects and to identify splicing factors associated with aberrant alternative splicing in COPD. For this purpose, we performed genome-wide RNA-sequencing analysis of bronchial brushings from 23 patients with mild-to-moderate COPD, 121 with severe COPD, and 23 non-COPD control subjects. We found a significant difference in the frequency of alternative splicing events in patients with mild-to-moderate and severe COPD compared with non-COPD control subjects. There were from two to eight times (depending on event type) more differential alternative splicing events in the severe than in the mild-to-moderate stage. The severe COPD samples showed less intron retention and more exon skipping. It is interesting that 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 patients with COPD and control subjects, 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 results provide a better understanding of COPD-related alternative splicing changes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento Alternativo / Doença Pulmonar Obstrutiva Crônica / Transcriptoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento Alternativo / Doença Pulmonar Obstrutiva Crônica / Transcriptoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article