Abstract
BackgroundTranscript dosage imbalance may influence the transcriptome. To gain insight into the role of altered gene expression in hereditary colorectal polyposis predisposition, in the present study we analyzed absolute and allele-specific expression (ASE) of adenomatous polyposis coli (APC) and mutY Homolog (MUTYH) genes.MethodsWe analyzed DNA and RNA extracted from peripheral blood mononuclear cells (PBMC) of 49 familial polyposis patients and 42 healthy blood donors selected according similar gender and age. Patients were studied for germline alterations in both genes using dHPLC, MLPA and automated sequencing. APC and MUTYH mRNA expression levels were investigated by quantitative Real-Time PCR (qRT-PCR) analysis using TaqMan assay and by ASE assays using dHPLC-based primer extension.ResultsTwenty out of 49 patients showed germline mutations: 14 in APC gene and six in MUTYH gene. Twenty-nine patients did not show mutations in both genes. Results from qRT-PCR indicated that gene expression of both APC and MUTYH was reduced in patients analyzed. In particular, a significant reduction in APC expression was observed in patients without APC germline mutation vs control group (P < 0.05) while APC expression in the mutation carrier patients, although lower compared to control individuals, did not show statistical significance. On the other hand a significant reduced MUTYH expression was detected in patients with MUTYH mutations vs control group (P < 0.05). Altered ASE of APC was detected in four out of eight APC mutation carriers. In particular one case showed a complete loss of one allele. Among APC mutation negative cases, 4 out of 13 showed a moderate ASE. ASE of MUTYH did not show any altered expression in the cases analyzed. Spearman’s Rho Test analysis showed a positive and significant correlation between APC and MUTYH genes both in cases and in controls (P = 0.020 and P < 0.001).ConclusionsAPC and MUTYH showed a reduced germline expression, not always corresponding to gene mutation. Expression of APC is decreased in mutation negative cases and this appears to be a promising indicator of FAP predisposition, while for MUTYH gene, mutation is associated to reduced mRNA expression. This study could improve the predictive genetic diagnosis of at-risk individuals belonging to families with reduced mRNA expression regardless of presence of mutation.Electronic supplementary materialThe online version of this article (doi:10.1186/s13046-015-0244-4) contains supplementary material, which is available to authorized users.
Highlights
Colorectal cancer (CRC) is one of the most frequent causes of cancer death worldwide [1, 2]
mutY Homolog (MUTYH) together with OGG1 and MTH1 is a component of DNA Base Excision Repair (BER) pathway that removes damaged bases generated by reactive oxygen species (ROS), capable to induce mutations commonly observed in cancerogenesis [7,8,9]
Mutation analysis of MUTYH gene was performed for cases negative at adenomatous polyposis coli (APC) mutation screening and detected sequence variants in six patients: two carriers of heterozygous variants (GD72 and GD155), three compound heterozygotes (GD68, GD82#1, GD82#2), and one carrier of exon 12 homozygous deletion (GD91) (Table 1)
Summary
Colorectal cancer (CRC) is one of the most frequent causes of cancer death worldwide [1, 2]. To gain insight in the correlation between APC and MUTYH mutations and altered expression, in the present study we investigated the role of dosage imbalance influencing the transcriptome of these two colon cancer-predisposing genes, performing an analysis of absolute and allele-specific expression in patients with different degrees of penetrance of hereditary colorectal disease. To understand the interaction between APC and BER pathway, we investigated the possible mutual modulation This exploratory study on correlation among mutational spectrum, gene dosage and phenotype, could improve the genetic diagnosis performing predictive testing of at-risk individuals belonging to families with reduced mRNA expression regardless of presence of mutation. To gain insight into the role of altered gene expression in hereditary colorectal polyposis predisposition, in the present study we analyzed absolute and allele-specific expression (ASE) of adenomatous polyposis coli (APC) and mutY Homolog (MUTYH) genes
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