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慢性阻塞性肺疾病相关基因中增加的转录本复杂性

Increased Transcript Complexity in Genes Associated with Chronic Obstructive Pulmonary Disease.

作者信息

Lackey Lela, McArthur Evonne, Laederach Alain

机构信息

Department of Biology, University of North Carolina, Chapel Hill, North Carolina, United States of America.

出版信息

PLoS One. 2015 Oct 19;10(10):e0140885. doi: 10.1371/journal.pone.0140885. eCollection 2015.

Abstract

Genome-wide association studies aim to correlate genotype with phenotype. Many common diseases including Type II diabetes, Alzheimer's, Parkinson's and Chronic Obstructive Pulmonary Disease (COPD) are complex genetic traits with hundreds of different loci that are associated with varied disease risk. Identifying common features in the genes associated with each disease remains a challenge. Furthermore, the role of post-transcriptional regulation, and in particular alternative splicing, is still poorly understood in most multigenic diseases. We therefore compiled comprehensive lists of genes associated with Type II diabetes, Alzheimer's, Parkinson's and COPD in an attempt to identify common features of their corresponding mRNA transcripts within each gene set. The SERPINA1 gene is a well-recognized genetic risk factor of COPD and it produces 11 transcript variants, which is exceptional for a human gene. This led us to hypothesize that other genes associated with COPD, and complex disorders in general, are highly transcriptionally diverse. We found that COPD-associated genes have a statistically significant enrichment in transcript complexity stemming from a disproportionately high level of alternative splicing, however, Type II Diabetes, Alzheimer's and Parkinson's disease genes were not significantly enriched. We also identified a subset of transcriptionally complex COPD-associated genes (~40%) that are differentially expressed between mild, moderate and severe COPD. Although the genes associated with other lung diseases are not extensively documented, we found preliminary data that idiopathic pulmonary disease genes, but not cystic fibrosis modulators, are also more transcriptionally complex. Interestingly, complex COPD transcripts are more often the product of alternative acceptor site usage. To verify the biological importance of these alternative transcripts, we used RNA-sequencing analyses to determine that COPD-associated genes are frequently expressed in lung and liver tissues and are regulated in a tissue-specific manner. Additionally, many complex COPD-associated genes are spliced differently between COPD and non-COPD patients. Our analysis therefore suggests that post-transcriptional regulation, particularly alternative splicing, is an important feature specific to COPD disease etiology that warrants further investigation.

摘要

全基因组关联研究旨在将基因型与表型相关联。许多常见疾病,包括II型糖尿病、阿尔茨海默病、帕金森病和慢性阻塞性肺疾病(COPD),都是复杂的遗传性状,有数百个不同的基因座与不同的疾病风险相关。识别与每种疾病相关的基因中的共同特征仍然是一项挑战。此外,在大多数多基因疾病中,转录后调控的作用,尤其是可变剪接,仍然知之甚少。因此,我们汇编了与II型糖尿病、阿尔茨海默病、帕金森病和COPD相关的基因综合列表,试图在每个基因集中识别其相应mRNA转录本的共同特征。SERPINA1基因是COPD公认的遗传风险因素,它产生11种转录变体,这在人类基因中是很罕见的。这使我们推测,其他与COPD相关的基因,以及一般的复杂疾病,在转录上具有高度多样性。我们发现,与COPD相关的基因在转录复杂性上有统计学意义的富集,这源于异常高水平的可变剪接,然而,II型糖尿病、阿尔茨海默病和帕金森病的基因没有显著富集。我们还确定了一组转录复杂的与COPD相关的基因(约40%),它们在轻度、中度和重度COPD之间存在差异表达。虽然与其他肺部疾病相关的基因没有广泛的文献记载,但我们发现初步数据表明,特发性肺病基因,而不是囊性纤维化调节基因,在转录上也更复杂。有趣的是,复杂的COPD转录本更常是可变受体位点使用的产物。为了验证这些可变转录本的生物学重要性,我们使用RNA测序分析来确定与COPD相关的基因在肺和肝组织中频繁表达,并以组织特异性方式受到调控。此外,许多与COPD相关的复杂基因在COPD患者和非COPD患者之间的剪接方式不同。因此,我们的分析表明,转录后调控,尤其是可变剪接,是COPD疾病病因学特有的一个重要特征,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d523/4610675/2d7bb47b2f3e/pone.0140885.g001.jpg

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