A Global Analysis of Tandem 3′UTRs in Eosinophilic Chronic Rhinosinusitis with Nasal Polyps

Background Alternative polyadenylation (APA) is emerging as a widespread mechanism of gene regulation. The usage of APA sites allows a single gene to encode multiple mRNA transcripts with different 3′-untranslated region (3′UTR) lengths. Many disease processes reflect the importance of the regulation of APA site switching. The objective of this study was to explore the profiling of tandem APA sites in nasal polyps compared with nasal uncinate process mucosa. Methods Sequencing of APA sites (SAPAS) based on second-generation sequencing technology was undertaken to investigate the use of tandem APA sites and identify gene expression patterns in samples from the nasal polyps and nasal uncinate process mucosa of two patients with chronic rhinosinusitis with nasal polyps. The findings of the SAPAS analysis were validated via quantitative reverse-transcription polymerase chain reaction (qRT-PCR). Results First, the results showed a switching of 3′UTR lengths in nasal polyps compared with nasal uncinate process mucosa. From the two patients, 105 genes that were detected in both patients in the nasal polyps were switched to distal poly(A) sites, and 90 such genes were switched to proximal poly(A) sites. Several Gene Ontology terms were enriched in the list of genes with switched APA sites, including transcription regulation, cell cycle, apoptosis, and metabolism. Second, we detected genes that showed differential expression with at least a 3-fold difference between nasal polyp tissue and nasal uncinate process mucosa. Between the two sample types, 627 genes exhibited differential expression. The qRT-PCR results confirmed our SAPAS results. Conclusion APA site-switching events of 3′UTRs are prevalent in nasal polyp tissue, and the regulation of gene expression mediated by APA may play an important role in the formation and persistence of nasal polyps. Our results may provide new insights into the possible pathophysiologic processes involved in nasal polyps.

[1]  H. Inoue,et al.  Gene‐expression profiles in human nasal polyp tissues and identification of genetic susceptibility in aspirin‐intolerant asthma , 2009, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[2]  M. Bakhshaee,et al.  Histopathologic characteristics of inferior turbinate vs ethmoidal polypin chronic rhinosinusitis. , 2011, Annals of diagnostic pathology.

[3]  B. Tian,et al.  Progressive lengthening of 3′ untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development , 2009, Proceedings of the National Academy of Sciences.

[4]  Xiaolu Yang,et al.  DEDD and DEDD2 associate with caspase-8/10 and signal cell death , 2003, Oncogene.

[5]  C. Lutz,et al.  Alternative mRNA polyadenylation in eukaryotes: an effective regulator of gene expression , 2011, Wiley interdisciplinary reviews. RNA.

[6]  P. Sharp,et al.  Proliferating Cells Express mRNAs with Shortened 3' Untranslated Regions and Fewer MicroRNA Target Sites , 2008, Science.

[7]  U. Hellman,et al.  Comparative proteome profiling of MCF10A and 184A1 human breast epithelial cells emphasized involvement of CDK4 and cyclin D3 in cell proliferation , 2009, Proteomics. Clinical applications.

[8]  David Haussler,et al.  The UCSC Genome Browser database: update 2010 , 2009, Nucleic Acids Res..

[9]  C. Bachert,et al.  Matrix metalloproteinases MMP‐7, MMP‐9 and their tissue inhibitor TIMP‐1: expression in chronic sinusitis vs nasal polyposis , 2004, Allergy.

[10]  R. Aebersold,et al.  Proteins of transcription factor ISGF-3: one gene encodes the 91-and 84-kDa ISGF-3 proteins that are activated by interferon alpha. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Bin Tian,et al.  A large-scale analysis of mRNA polyadenylation of human and mouse genes , 2005, Nucleic acids research.

[12]  Cole Trapnell,et al.  Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.

[13]  Alan Agresti,et al.  Categorical Data Analysis , 2003 .

[14]  Z. Zhai,et al.  The p53‐inducible E3 ubiquitin ligase p53RFP induces p53‐dependent apoptosis , 2006, FEBS letters.

[15]  C. Mayr,et al.  Widespread Shortening of 3′UTRs by Alternative Cleavage and Polyadenylation Activates Oncogenes in Cancer Cells , 2009, Cell.

[16]  David Baltimore,et al.  Function of miR-146a in Controlling Treg Cell-Mediated Regulation of Th1 Responses , 2010, Cell.

[17]  C. Bachert,et al.  Pathogenesis of chronic rhinosinusitis: inflammation. , 2011, The Journal of allergy and clinical immunology.

[18]  Luo Zhang,et al.  Expression of Survivin and Enhanced Polypogenesis in Nasal Polyps , 2008, American journal of rhinology.

[19]  Chong-Jian Chen,et al.  Differential genome-wide profiling of tandem 3' UTRs among human breast cancer and normal cells by high-throughput sequencing. , 2011, Genome research.

[20]  D. Kennedy,et al.  Staging for Rhinosinusitis , 1997, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[21]  D. Hamilos Chronic rhinosinusitis: epidemiology and medical management. , 2011, The Journal of allergy and clinical immunology.

[22]  M. Saavedra,et al.  Protein Microarray Analysis of Nasal Polyps from Aspirin-Sensitive and Aspirin-Tolerant Patients with Chronic Rhinosinusitis , 2009, American journal of rhinology & allergy.

[23]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.

[24]  S. Wenzel,et al.  The role of cytokines in chronic rhinosinusitis with nasal polyps , 2008, Current opinion in otolaryngology & head and neck surgery.

[25]  N. Hayward,et al.  Identification of ARHGEF17, DENND2D, FGFR3, and RB1 mutations in melanoma by inhibition of nonsense‐mediated mRNA decay , 2008, Genes, chromosomes & cancer.

[26]  R. Quigg,et al.  MicroRNA‐377 is up‐regulated and can lead to increased fibronectin production in diabetic nephropathy , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[27]  Y. Kurono,et al.  IL-4 and TNF-alpha increased the secretion of eotaxin from cultured fibroblasts of nasal polyps with eosinophil infiltration. , 2007, Rhinology.

[28]  W. Fokkens,et al.  Role of Innate Immunity in the Pathogenesis of Chronic Rhinosinusitis: Progress and New Avenues , 2012, Current Allergy and Asthma Reports.

[29]  C. Bachert,et al.  Direct demonstration of delayed eosinophil apoptosis as a mechanism causing tissue eosinophilia. , 1997, Journal of immunology.

[30]  M. Salto‐Tellez,et al.  The expression of RUNX3 in colorectal cancer is associated with disease stage and patient outcome , 2009, British Journal of Cancer.

[31]  A. Fortuna,et al.  Measurement of asthma control according to global initiative for asthma guidelines: a comparison with the asthma control questionnaire , 2012, Respiratory Research.

[32]  Mara L. Hartsperger,et al.  Cis-Acting Polymorphisms Affect Complex Traits through Modifications of MicroRNA Regulation Pathways , 2012, PloS one.

[33]  N. Proudfoot Ending the message: poly(A) signals then and now. , 2011, Genes & development.

[34]  L. Bing,et al.  Gene expression profiles of nasal polyps associated with allergic rhinitis. , 2009, American journal of otolaryngology.

[35]  M. Mäki,et al.  TGF-β induces the expression of SAP30L, a novel nuclear protein , 2003, BMC Genomics.

[36]  V. Katanaev The Wnt/Frizzled GPCR signaling pathway , 2010, Biochemistry (Moscow).

[37]  W. Fokkens,et al.  EP3OS 2007: European position paper on rhinosinusitis and nasal polyps 2007. A summary for otorhinolaryngologists. , 2007, Rhinology.

[38]  K. Nishida,et al.  Mechanisms and consequences of alternative polyadenylation. , 2011, Molecules and Cells.

[39]  M. Fraczek,et al.  A microarray study of gene expression profiles in nasal polyps. , 2011, Auris, nasus, larynx.

[40]  Mary Goldman,et al.  The UCSC Genome Browser database: update 2011 , 2010, Nucleic Acids Res..

[41]  P. Milani,et al.  SOD1 Transcriptional and Posttranscriptional Regulation and Its Potential Implications in ALS , 2011, Neurology research international.