Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways

Background Genetic studies of human lung function and Chronic Obstructive Pulmonary Disease have identified a highly significant and reproducible signal on 4q24. It remains unclear which of the two candidate genes within this locus may regulate lung function: GSTCD, a gene with unknown function, an...

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Main Authors: Kheirallah, Alexander K., de Moor, Cornelia H., Faiz, Alen, Sayers, Ian, Hall, Ian P.
Format: Article
Published: BioMed Central 2017
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Online Access:https://eprints.nottingham.ac.uk/41626/
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author Kheirallah, Alexander K.
de Moor, Cornelia H.
Faiz, Alen
Sayers, Ian
Hall, Ian P.
author_facet Kheirallah, Alexander K.
de Moor, Cornelia H.
Faiz, Alen
Sayers, Ian
Hall, Ian P.
author_sort Kheirallah, Alexander K.
building Nottingham Research Data Repository
collection Online Access
description Background Genetic studies of human lung function and Chronic Obstructive Pulmonary Disease have identified a highly significant and reproducible signal on 4q24. It remains unclear which of the two candidate genes within this locus may regulate lung function: GSTCD, a gene with unknown function, and/or INTS12, a member of the Integrator Complex which is currently thought to mediate 3’end processing of small nuclear RNAs. Results We found that, in lung tissue, 4q24 polymorphisms associated with lung function correlate with INTS12 but not neighbouring GSTCD expression. In contrast to the previous reports in other species, we only observed a minor alteration of snRNA processing following INTS12 depletion. RNAseq analysis of knockdown cells instead revealed dysregulation of a core subset of genes relevant to airway biology and a robust downregulation of protein synthesis pathways. Consistent with this, protein translation was decreased in INTS12 knockdown cells. In addition, ChIPseq experiments demonstrated INTS12 binding throughout the genome, which was enriched in transcriptionally active regions. Finally, we defined the INTS12 regulome which includes genes belonging to the protein synthesis pathways. Conclusion INTS12 has functions beyond the canonical snRNA processing. We show that it regulates translation by regulating the expression of genes belonging to protein synthesis pathways. This study provides a detailed analysis of INTS12 activities on a genome-wide scale and contributes to the biology behind the genetic association for lung function at 4q24.
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spelling nottingham-416262020-05-04T18:38:36Z https://eprints.nottingham.ac.uk/41626/ Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways Kheirallah, Alexander K. de Moor, Cornelia H. Faiz, Alen Sayers, Ian Hall, Ian P. Background Genetic studies of human lung function and Chronic Obstructive Pulmonary Disease have identified a highly significant and reproducible signal on 4q24. It remains unclear which of the two candidate genes within this locus may regulate lung function: GSTCD, a gene with unknown function, and/or INTS12, a member of the Integrator Complex which is currently thought to mediate 3’end processing of small nuclear RNAs. Results We found that, in lung tissue, 4q24 polymorphisms associated with lung function correlate with INTS12 but not neighbouring GSTCD expression. In contrast to the previous reports in other species, we only observed a minor alteration of snRNA processing following INTS12 depletion. RNAseq analysis of knockdown cells instead revealed dysregulation of a core subset of genes relevant to airway biology and a robust downregulation of protein synthesis pathways. Consistent with this, protein translation was decreased in INTS12 knockdown cells. In addition, ChIPseq experiments demonstrated INTS12 binding throughout the genome, which was enriched in transcriptionally active regions. Finally, we defined the INTS12 regulome which includes genes belonging to the protein synthesis pathways. Conclusion INTS12 has functions beyond the canonical snRNA processing. We show that it regulates translation by regulating the expression of genes belonging to protein synthesis pathways. This study provides a detailed analysis of INTS12 activities on a genome-wide scale and contributes to the biology behind the genetic association for lung function at 4q24. BioMed Central 2017-03-23 Article PeerReviewed Kheirallah, Alexander K., de Moor, Cornelia H., Faiz, Alen, Sayers, Ian and Hall, Ian P. (2017) Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways. BMC Genomics, 18 (1). p. 248. ISSN 1471-2164 Integrator Complex INTS12 snRNA processing Protein synthesis Regulation of gene expression Pathway dysregulation Histone modification Accessible chromatin Transcription http://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-017-3628-3 doi:10.1186/s12864-017-3628-3 doi:10.1186/s12864-017-3628-3
spellingShingle Integrator Complex
INTS12
snRNA processing
Protein synthesis
Regulation of gene expression
Pathway dysregulation
Histone modification
Accessible chromatin
Transcription
Kheirallah, Alexander K.
de Moor, Cornelia H.
Faiz, Alen
Sayers, Ian
Hall, Ian P.
Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title_full Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title_fullStr Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title_full_unstemmed Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title_short Lung function associated gene Integrator Complex subunit 12 regulates protein synthesis pathways
title_sort lung function associated gene integrator complex subunit 12 regulates protein synthesis pathways
topic Integrator Complex
INTS12
snRNA processing
Protein synthesis
Regulation of gene expression
Pathway dysregulation
Histone modification
Accessible chromatin
Transcription
url https://eprints.nottingham.ac.uk/41626/
https://eprints.nottingham.ac.uk/41626/
https://eprints.nottingham.ac.uk/41626/