Skip to main content

Advertisement

Log in

Prioritization of candidate SNPs in colon cancer using bioinformatics tools: An alternative approach for a cancer biologist

  • Published:
Interdisciplinary Sciences: Computational Life Sciences Aims and scope Submit manuscript

Abstract

The genetics of human phenotype variation and especially, the genetic basis of human complex diseases could be understood by knowing the functions of Single Nucleotide Polymorphisms (SNPs). The main goal of this work is to predict the deleterious non-synonymous SNPs (nsSNPs), so that the number of SNPs screened for association with disease can be reduced to that most likely alters gene function. In this work by using computational tools, we have analyzed the SNPs that can alter the expression and function of cancerous genes involved in colon cancer. To explore possible relationships between genetic mutation and phenotypic variation, different computational algorithm tools like Sorting Intolerant from Tolerant (evolutionary-based approach), Polymorphism Phenotyping (structure-based approach), PupaSuite, UTRScan and FASTSNP were used for prioritization of high-risk SNPs in coding region (exonic nonsynonymous SNPs) and non-coding regions (intronic and exonic 5′ and 3′-untranslated region (UTR) SNPs). We developed semi-quantitative relative ranking strategy (non availability of 3D structure) that can be adapted to a priori SNP selection or post hoc evaluation of variants identified in whole genome scans or within haplotype blocks associated with disease. Lastly, we analyzed haplotype tagging SNPs (htSNPs) in the coding and untranslated regions of all the genes by selecting the force tag SNPs selection using iHAP analysis. The computational architecture proposed in this review is based on integrating relevant biomedical information sources to provide a systematic analysis of complex diseases. We have shown a “real world” application of interesting existing bioinformatics tools for SNP analysis in colon cancer.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Andrawiss, M. 2005. First phase of HapMap project already helping drug discovery. Nat Rev Drug Discov 4, 947.

    Article  PubMed  CAS  Google Scholar 

  2. Balasubramanian, S., Xia, Y., Freinkman, E., Gerstein, M. 2005. Sequence variation in G-Proteincoupled receptors: Analysis of single nucleotide polymorphisms. Nucleic Acids Res 33, 1710–1721.

    Article  PubMed  CAS  Google Scholar 

  3. Bao, L., Cui, Y. 2006. Functional impacts of nonsynonymous single nucleotide polymorphisms: Selective constraint and structural environments. FEBS Lett 580, 1231–1234.

    Article  PubMed  CAS  Google Scholar 

  4. Barnetson, R.A., Cartwright, N., Van, V.A., Haq, N., Drew, K., Farrington, S., Williams, N., Warner, J., Campbell, H., Porteous, M.E., Dunlop, M.G. 2008. Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer. Hum Mutat 29, 367–374.

    Article  PubMed  CAS  Google Scholar 

  5. Brooks-Wilson, A.R., Kaurah, P., Suriano, G. 2004. Germline Ecadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria. J Med Genet 41, 508–517.

    Article  PubMed  CAS  Google Scholar 

  6. Chasman, D., Adams, R.M. 2001. Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation. J Mol Biol 307, 683–706.

    Article  PubMed  CAS  Google Scholar 

  7. Chen-Shtoyerman, R., Theodor, L., Harmati, E., Friedman, E., Dacka, S., Kopelman, Y., Sternberg, A., Zarivach, R., Bar-Meir, S., Fireman, Z. 2003. Genetic analysis of familial colorectal cancer in Israeli Arabs. Hum Mutat 21, 446–447.

    Article  PubMed  CAS  Google Scholar 

  8. Colombino, M., Cossu, A., Arba, A., Manca, A., Curci, A., Avallone, A., Comella, G., Botti, G., Scintu, F., Amoruso, M., D’Abbicco, D., d’Agnessa, M.R., Spanu, A., Tanda, F., Palmieri, G. 2003. Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: Detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. Ann Oncol 14, 1530–1536.

    Article  PubMed  CAS  Google Scholar 

  9. Conde, L., Vaquerizas, J.M., Dopazo, H., Arbiza, L., Reumers, J., Rousseau, F., Schymkowitz, J., Dopazo, J. 2006. PupaSuite: Finding functional single nu cleotide polymorphisms for large-scale genotyping purposes. Nucleic Acids Res 34, W621–W625.

    Article  PubMed  CAS  Google Scholar 

  10. Conde, L., Vaquerizas, J.M., Ferrer-Costa, C., Orozco, M., Dopazo, J. 2005. PupasView: A visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping Purposes. Nucleic Acids Res 33, W501–W505.

    Article  PubMed  CAS  Google Scholar 

  11. Cravo, M., Afonso, A.J., Lage, P., Albuquerque, C., Maia, L., Lacerda, C., Fidalgo, P., Chaves, P., Cruz, C., Nobre-Leitao, C. 2002. Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: Implications for genetic testing. Gut 50, 405–412.

    Article  PubMed  CAS  Google Scholar 

  12. Doss, C.G.P., Sudandiradoss, C., Rajasekaran, R., Prohit, R., Ramanathan, K., Sethumadhavan, R. 2008a. Identification and structural comparison of deleterious mutations in nsSNPs of ABL1 gene in chronic myeloid leukemia: A bioinformatics study. Journal of Biomedical Informatics 41, 607–612.

    Article  CAS  Google Scholar 

  13. Doss, C.G.P., Sudandiradoss, C., Rajasekaran, R., choudhury, P., Sinha, P., Hota, P., Batra, U.P., Sethumadhavan, R. 2008b. Application of computational algorithm tools to identify functional SNPs. Functional and Integrative Genomics 8, 309–316.

    Article  CAS  Google Scholar 

  14. Doss, C.G.P., Rajasekaran, R., Sudandiradoss, C., Ramanathan, K., Prohit, R., Sethumadhavan, R. 2008c. A novel computational and structural analysis of nsSNPs in CFTR gene. Genomic Medicine 2, 23–32.

    Article  Google Scholar 

  15. Doss, C.G.P., Sethumadhavan, R. 2009a. Structural and Functional analysis of deleterious nsSNPs in PAH associated with Phenylketonuria. Advance Science Letters 2, 364–371.

    CAS  Google Scholar 

  16. Doss, C.G.P., Sethumadhavan, R. 2009b. Functional and structural characterization of polymorphisms in MSH2 gene using computational tools. Journal of Bionanoscience 3, 1–9.

    Article  CAS  Google Scholar 

  17. Doss. C.G.P., Sethumadhavan, R. 2009c. Investigation on the role of nsSNPs in HNPCC genes — A Bioinformatics approach. BMC Journal of biomedical science 16, 42.

    Article  CAS  Google Scholar 

  18. Ellison, A.R., Lofing, J., Bitter, G.A. 2001. Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae. Hum Mol Genet 10, 1889–1900.

    Article  PubMed  CAS  Google Scholar 

  19. Ferrer-Costa, C., Gelpi, J.L., Zamakola, L., Parraga, I., de la Cruz, X., Orozco. M. 2005. PMUT: A web-based tool for the annotation of pathological mutations on proteins. Bioinformatics 21, 3176–3178.

    Article  PubMed  CAS  Google Scholar 

  20. Fodde, R., Smits, R., Clevers, H. 2001. APC, signal transduction and genetic instability in colorectal cancer. Nat Rev Cancer 1, 55–67.

    Article  PubMed  CAS  Google Scholar 

  21. Fredman, D., Munns, G., Rios, D., Sjöholm, F., Siegfried, M., Lenhard, B., Lehväslaiho, H., Brookes, A.J. 2004. HGVbase: A curated resource describing human DNA variation and phenotype relationships. Nucleic Acids Res 32, D516–D519.

    Article  PubMed  CAS  Google Scholar 

  22. Fullerton, S.M., Buchanan, A.V., Sonpar, V.A., Taylor, S.L., Smith, J.D., Carlson, C.S., Salomaa, V., Stengard, J.H., Boerwinkle, E., Clark, A.G., Nickerson, D.A., Weiss, K.M. 2004. The effects of scale: Variation in the APOA1/C3/A4/A5 gene Cluster. Hum Gene 115, 36–56.

    Article  CAS  Google Scholar 

  23. Futrea, P.A., Coin, L., Marshall, M., Down, T., Hubbard, T., Wooster, R., Rahman, N., Stratton, M.R. 2004. A census of human cancer genes. Nat Rev Cancer 4, 177–183.

    Article  CAS  Google Scholar 

  24. Gorlov, I.P., Gorlova, O.Y., Frazier, M.L., Amos, C.I. 2003. Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers. Am J Hum Genet 73, 1157–1161.

    Article  PubMed  CAS  Google Scholar 

  25. Gryfe, R. 2006. Clinical implications of ouradvancing knowledge of colorectal cancer genetics: Inherited syndromes, prognosis, prevention, screening and therapeutics. Surgical Clinics of North America 86, 787–817.

    Article  PubMed  Google Scholar 

  26. Hudson, T.J. 2003. Wanted: Regulatory SNPs. Nat Genet 33, 439–440.

    Article  PubMed  CAS  Google Scholar 

  27. Huret, J.L., Dessen, P., Bernheim, A. 2003. Atlas of genetics and cytogenetics in oncology and haematology. Nucleic Acids Res 31, 272–274.

    Article  PubMed  CAS  Google Scholar 

  28. Jemal, A., Siegel, R., Ward, E., Murray, T., Xu, J., Thun, M.J. 2007. Cancer statistics. A Cancer J Clin 57, 43.

    Article  Google Scholar 

  29. Kanetsky, P.A., Ge, F., Najarian, D., Swoyer, J., Panossian, S., Schuchter, L., Holmes, R., Guerry, D., Rebbeck, T.R. 2004. Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach. Cancer Epidemiol Biomarkers Prev 13, 808–819.

    PubMed  CAS  Google Scholar 

  30. Karchin, R., Kelly, L., Sali, A. 2005a. Improving functional annotation of non-synonymous SNPs with information theory. Pac Symp Biocomput 10, 397–408.

    Article  Google Scholar 

  31. Karchin, R., Diekhans, M., Kelly, L. Thomas, D.J., Pieper, U., Eswar, N., Haussler, D., Sali, A. 2005b. LS-SNP: Large-scale annotation of coding non-synonymous SNPs based on multiple information sources. Bioinformatics 21, 2814–2820.

    Article  PubMed  CAS  Google Scholar 

  32. Kariola, R., Hampel, H., Frankel, W.L., Raevaara, T.E., de la Chapelle, A., Nyström-Lahti, M. 2004. MMSH6 missense mutations are often associated with no or low cancer susceptibility. Br J Can 91, 1287–1292.

    Article  CAS  Google Scholar 

  33. Krawczak, M., Ball, E.V., Fenton, I., Stenson, P.D., Abeysinghe, S., Thomas, N., Strachan, T., Read, A.P., Cooper, D.N. 2000. Human gene mutation database — A biomedical information and research resource. Hum Mutat 15, 45–51.

    Article  PubMed  CAS  Google Scholar 

  34. Kumar, P., Henikoff, S., Ng, P.C. 2009. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nature Protocols 4, 1073–1081.

    Article  PubMed  CAS  Google Scholar 

  35. Lynch, H.T., de la Chapelle, A. 2003. Hereditary colorectal cancer. N Engl J Med 348, 919–932.

    Article  PubMed  CAS  Google Scholar 

  36. Mooney, S. 2005. Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis. Brief Bioinform 6, 44–56.

    Article  PubMed  CAS  Google Scholar 

  37. Moreno-Estrada, A., Casals, F., Ramirez-Soriano, A., Oliva, B., Calafell, F., Bertranpetit, J., Bosch, E. 2008. Signatures of selection in the human olfactory receptor OR5I1 gene. Mol Biol Evol 25, 144–154.

    Article  PubMed  CAS  Google Scholar 

  38. Ng, P.C., Henikoff, S. 2003. SIFT: Predicting amino acid changes that affect protein Function. Nucleic Acids Res 31, 3812–3814.

    Article  PubMed  CAS  Google Scholar 

  39. Ng, P.C., Henikoff, S. 2006. Predicting the effects of amino acid substitutions on protein function. Annu Rev Genomics Hum Genet 7, 61–80.

    Article  PubMed  CAS  Google Scholar 

  40. Nowak, R. 1994. Mining treasures from ‘junk DNA’. Science 263, 608–610.

    Article  PubMed  CAS  Google Scholar 

  41. Nystrom-Lahti, M., Perrera, C., Räschle, M., Panyushkina-Seiler, E., Marra, G., Curci, A., Quaresima, B., Costanzo, F.D., Urso, M., Venuta, S., Jiricny, J. 2002. Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer. Genes Chromosomes Cancer 33, 160–167.

    Article  PubMed  CAS  Google Scholar 

  42. Ohmiya, N., Matsumoto, S., Yamamoto, H., Baranovskaya, S., Malkhosyan, S.R., Perucho, M. 2001. Germline and somatic mutations in hMSH6 and hMSH3 in gastrointestinal cancers of the microsatellite mutator phenotype. Gene 272, 301–313.

    Article  PubMed  CAS  Google Scholar 

  43. Pesole, G., Liuni, S., 1999. Internet resources for the functional analysis of 5′ and 3′untranslated regions of eukaryotic mRNA. TIG 15, 378.

    Article  PubMed  CAS  Google Scholar 

  44. Pesole, G., Liuni, S., Grillo, G., Licciulli, F., Mignone, F., Gissi, C., Saccone, C. 2002. UTRdb and UTRsite: Specialized databases of sequences and functional elements of 5′ and 3′ untranslated regions of eukaryotic mRNAs. Nucleic Acids Res 30, 335–340.

    Article  PubMed  CAS  Google Scholar 

  45. Peterlongo, P., Nafa, K., Lerman, G.S. 2003. MSH6 germline mutations are rare in colorectal cancer families. Int J Cancer 107, 571–579.

    Article  PubMed  CAS  Google Scholar 

  46. Plaschke, J., Kruppa, C., Tischler, R. 2000. Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer. Int J Cancer 85, 606–613.

    Article  PubMed  CAS  Google Scholar 

  47. Raevaara, T.E., Korhonen, M.K., Lohi, H., Hampel, H., Lynch, E., Lönnqvist, K.E., Holinski-Feder, E., Sutter, C., McKinnon, W., Duraisamy, S., Gerdes, A.M., Peltomäki, P., Kohonen-Ccorish, M., Mangold, E., Macrae, F., Greenblatt, M., de la Chapelle, A., Nystrom, M. 2005. Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1. Gastroenterology 129, 537–549.

    PubMed  CAS  Google Scholar 

  48. Ramensky, V., Pork, P., Sunyaev, S. 2002. Human nonsynonymous SNPs: Server and survey. Nucleic Acids Research 30, 3894–3900.

    Article  PubMed  CAS  Google Scholar 

  49. Renkonen, E., Lohi, H., Jarvinen, H.J., Mecklin, J.P., Peltomaki, P. 2004. Novel splicing associations of hereditary colon cancer related DNA mismatch repair gene mutations. J Med Genet 41, e95.

    Article  PubMed  CAS  Google Scholar 

  50. Reumers, J., Conde, L., Medina, I., Maurer-Stroh, S., Durme, J.V., Dopazo, J., Rousseau, F., Schymkowitz, J. 2008. Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases. Nucl Acids Res 36, D825–D829.

    Article  PubMed  CAS  Google Scholar 

  51. Reumers, J., Maurer-Stroh, S., Schymkowitz, J., Rousseau, F. 2006. SNPeffect v2.0: A new step in investigating the molecular phenotypic effects of human non-synonymous SNPs. Bioinformatics 22, 2183–2185.

    Article  PubMed  CAS  Google Scholar 

  52. Ricciardiello, L., Boland, C.R. 2005. Lynch syndrome (hereditary nonpolyposis colorectal cancer): Current concepts and approaches to management. Curr Gastroenterol Rep 7, 412–420.

    Article  PubMed  Google Scholar 

  53. Richard, J.D., Patricia, B.M., Mark, J.C., Saqi, M.A.S. 2006. Predicting deleterious nsSNPs: An analysis of sequence and structural attributes. BMC Bioinformatics 7, 217.

    Article  CAS  Google Scholar 

  54. Scartozzi, M., Bianchi, F., Rosati, S., Galizia, E., Antolini, A., Loretelli, C., Piga, A., Bearzi, I., Cellerino, R., Porfiri, E. 2002. Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: Correlation with microsatellite instability and abnormalities of mismatch repair protein expression. J Clin Oncol 20, 1203–1208.

    Article  PubMed  CAS  Google Scholar 

  55. Slabinski, L., Jaroszewski, L., Rodrigues, A.P., Rychlewski, L., Wilson, I.A., Lesley, S.A., Godzik, A. 2007. The challenge of protein structure determination — lessons from structural genomics. Protein Sci 16, 2472–2482.

    Article  PubMed  CAS  Google Scholar 

  56. Smigielski, E.M., Sirotkin, K., Ward, M., Sherry, S.T. 2000. dbSNP: A database of single nucleotide polymorphisms. Nucleic Acids Res 28, 352–355.

    Article  PubMed  CAS  Google Scholar 

  57. Sonenberg, N. 1994. mRNA translation: Influence of the 5′ and 3′ untranslated Regions. Curr Opin Genet 4, 310–315.

    Article  CAS  Google Scholar 

  58. Song, C.M., Yeo, B.H., Tantoso, E., Yang, Y., Lim, Y.P., Li, K.B., Rajagopal, G. 2006. iHAP — integrated haplotype analysis pipeline for characterizing the haplotype structure of genes. BMC Bioinformatics 7, 525.

    Article  PubMed  CAS  Google Scholar 

  59. Stumpf, M.P.H. 2004. Haplotype diversity and SNP frequency dependence in the description of genetic variation. Eur J Hum Genet 12, 469–477.

    Article  PubMed  CAS  Google Scholar 

  60. Sunyaev, S., Ramensky, V., Bork, P. 2001. Towards a structural basis of human non-synonymous single nucleotide polymorphisms. Trends Genet 16, 198–200.

    Article  Google Scholar 

  61. The International HapMap Consortium. 2003. The International HapMap Project. Nature 426, 789–796.

    Article  CAS  Google Scholar 

  62. Thomas, P.D., Campbell, M.J., Kejariwal, A., Mi, H., Karlak, B., Daverman, R., Diemer, K., Muruganujan, A., Narechania, A. 2003. PANTHER: A library of protein families and subfamilies indexed by function. Genome Res 13, 2129–2141.

    Article  PubMed  CAS  Google Scholar 

  63. Vakser, I.A., Kundrotas, P. 2008. Predicting 3D structures of protein-protein complexes. Curr Pharm Biotechnol 9, 57–66.

    Article  PubMed  CAS  Google Scholar 

  64. Xi, T., Jones, I.M., Mohrenweiser, H.W. 2005. Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function. Genomics 83, 970–979.

    Article  CAS  Google Scholar 

  65. Yuan, H.Y., Chiou, J.J., Tseng, W.J., Liu, C.H., Liu, C.K., Lin, Y.J., Wang, H.H., Yao, A., Chen, Y.T., Hsu, C.N. 2006. FASTSNP: An always up-to-date and extendable service for SNP function analysis and prioritization. Nucleic Acids Res 34, W635–W641.

    Article  PubMed  CAS  Google Scholar 

  66. Yue, P., Melamud, E., Moult, J. 2006. SNPs3D: Candidate gene and SNP selection for association studies. BMC Bioinformatics 7, 166.

    Article  PubMed  CAS  Google Scholar 

  67. Zhang, E.Y., Fu, D.J., Pak, Y.A., Ste wart, T.T., Mukhopadhyay, N., Wrighton, S.A., Hillgren, K.M. 2004. Genetic polymorphisms in human protondependent dipeptide transporter PEPT1: Implications for the functional role of Pro586. J Pharmacol Exp Ther 310, 437–445.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Rao Sethumadhavan.

Rights and permissions

Reprints and permissions

About this article

Cite this article

George Priya Doss, C., Rajasekaran, R., Arjun, P. et al. Prioritization of candidate SNPs in colon cancer using bioinformatics tools: An alternative approach for a cancer biologist. Interdiscip Sci Comput Life Sci 2, 320–346 (2010). https://doi.org/10.1007/s12539-010-0003-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12539-010-0003-3

Key words

Navigation