In Silico Post Translational Analysis of Functional Single Nucleotide Alterations in Human TERT Gene Associated with Acute Myeloid Leukemia

Authors

  • Anam Munir Department of Zoology, Division of Science and Technology, University of Education Township, Lahore, Pakistan
  • Afia Muhammad Akram Department of Zoology, Division of Science and Technology, University of Education Township, Lahore, Pakistan
  • Khansa Jamil Department of Zoology, Division of Science and Technology, University of Education Township, Lahore, Pakistan
  • Asma Tahir Department of Zoology, Division of Science and Technology, University of Education Township, Lahore, Pakistan

DOI:

https://doi.org/10.54393/pbmj.v6i05.881

Keywords:

AML, TERT, in silico, SNPs, NCBI

Abstract

Acute myeloid leukemia (AML) refers to a diverse assemblage of hematological malignancies that constitute clonal expansion of immature myeloid progenitor cells in the peripheral blood and bone marrow. TERT gene ensures telomeres maintenance, chromosome stability and prevention of malignancy. The TERT gene has several single nucleotide polymorphisms (SNPs) that have been linked to a number of diseases, including AML. Objective: To classify the harmful TERT gene mutations, and to analyze them using various computational approaches at structural, functional and translational expression levels Methods: National Centre for Biotechnology Information (NCBI) database was used to retrieve nsSNPs of TERT gene (Q53H, V170M, A184T, S255Y, A288V, H412Y, I540M, R631W) reported in AML and they were analyzed using various bioinformatics tools. Results: In this in silico analysis, it was observed that seven out of eight SNPs had a damaging effect; they could affect the protein stability, protein-protein interactions, hydrophobicity, protein folding, three-dimensional structure, secondary structure and conservation profile. 3D models were generated and validated by various tools and the structural effect of these alterations was observed on protein function that was destabilizing to the RNA folding, protein-protein interactions and other functionally associated proteins. Analysis of post translational modifications showed no significant effect of these mutations. Conclusions: These SNPs could be used in future as potential targets in disease diagnosis, biological markers and protein studies.

References

Obeagu EI and Babar Q. Acute Myeloid Leukaemia (AML): The Good, the Bad, and the Ugly. International Journal of Current Research and Medical Sciences. 2021; 7(7): 29-41.

Bullinger L, Döhner K, Döhner H. Genomics of acute myeloid leukemia diagnosis and pathways. Journal of Clinical Oncology. 2017 Mar; 35(9): 934-46. doi: 10.1200/JCO.2016.71.2208. DOI: https://doi.org/10.1200/JCO.2016.71.2208

Irish W, Ryan M, Gache L, Gunnarsson C, Bell T, Shapiro M. Acute myeloid leukemia: a retrospective claims analysis of resource utilization and expenditures for newly diagnosed patients from first-line induction to remission and relapse. Current Medical Research and Opinion. 2017 Mar; 33(3): 519-27. doi: 10.1080/03007995.2016.1267615. DOI: https://doi.org/10.1080/03007995.2016.1267615

Levin M, Stark M, Ofran Y, Assaraf YG. Deciphering molecular mechanisms underlying chemoresistance in relapsed AML patients: Towards precision medicine overcoming drug resistance. Cancer Cell International. 2021 Dec; 21(1): 1-6. doi: 10.1186/s12935-021-01746-w. DOI: https://doi.org/10.1186/s12935-021-01746-w

Kabel A, Zamzami F, Al-Talhi M, Al-Dwila K, Hamza R. Acute myeloid leukemia: A focus on risk factors, clinical presentation, diagnosis and possible lines of management. Cancer Research Treatment. 2017; 5: 62-7.

Tebbi CK. Etiology of acute leukemia: A review. Cancers. 2021 May; 13(9): 2256. doi: 10.3390/cancers13092256. DOI: https://doi.org/10.3390/cancers13092256

Rehman A, Akram AM, Chaudhary A, Sheikh N, Hussain Z, Alsanie WF, et al. RUNX1 mutation and elevated FLT3 gene expression cooperates to induce inferior prognosis in cytogenetically normal acute myeloid leukemia patients. Saudi Journal of Biological Sciences. 2021 Sep; 28(9): 4845-51. doi: 10.1016/j.sjbs.2021.07.012. DOI: https://doi.org/10.1016/j.sjbs.2021.07.012

Ly H. Telomere dynamics in induced pluripotent stem cells: potentials for human disease modeling. World Journal of Stem Cells. 2011 Oct; 3(10): 89. doi: 10.4252/wjsc.v3.i10.89. DOI: https://doi.org/10.4252/wjsc.v3.i10.89

Dratwa M, Wysoczańska B, Łacina P, Kubik T, Bogunia-Kubik K. TERT—regulation and roles in cancer formation. Frontiers in Immunology. 2020 Nov; 11: 589929. doi: 10.3389/fimmu.2020.589929. DOI: https://doi.org/10.3389/fimmu.2020.589929

Akincilar SC, Unal B, Tergaonkar V. Reactivation of telomerase in cancer. Cellular and Molecular Life Sciences. 2016 Apr; 73: 1659-70. doi: 10.1007/s00018-016-2146-9. DOI: https://doi.org/10.1007/s00018-016-2146-9

Ding D, Zhou J, Wang M, Cong YS. Implications of telomere‐independent activities of telomerase reverse transcriptase in human cancer. The FEBS Journal. 2013 Jul; 280(14): 3205-11. doi: 10.1111/febs.12258. DOI: https://doi.org/10.1111/febs.12258

Barthel FP, Wei W, Tang M, Martinez-Ledesma E, Hu X, Amin SB, et al. Systematic analysis of telomere length and somatic alterations in 31 cancer types. Nature Genetics. 2017 Mar; 49(3): 349-57. doi: 10.1038/ng.3781. DOI: https://doi.org/10.1038/ng.3781

Du HY, Pumbo E, Ivanovich J, An P, Maziarz RT, Reiss UM, et al. TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements. Blood, The Journal of the American Society of Hematology. 2009 Jan; 113(2): 309-16. doi: 10.1182/blood-2008-07-166421. DOI: https://doi.org/10.1182/blood-2008-07-166421

Abdelrahman AH, Eid MM, Hassan M, Eid OM, AbdelKader RM, AlAzhary NM, et al. Telomerase reverse transcriptase gene amplification in hematological malignancies. Egyptian Journal of Medical Human Genetics. 2019 Dec; 20: 1-9. doi: 10.1186/s43042-019-0036-z. DOI: https://doi.org/10.1186/s43042-019-0036-z

Dana H, Mahmoodi Chalbatani G, Gharagouzloo E, Miri SR, Memari F, Rasoolzadeh R, et al. In silico analysis, molecular docking, molecular dynamic, cloning, expression and purification of chimeric protein in colorectal cancer treatment. Drug Design, Development and Therapy. 2020 Jan: 309-29. doi: 10.2147/DDDT.S231958. DOI: https://doi.org/10.2147/DDDT.S231958

Shihab HA, Gough J, Cooper DN, Stenson PD, Barker GL, Edwards KJ, et al. Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models. Human Mutation. 2013 Jan; 34(1): 57-65. doi: 10.1002/humu.22225. DOI: https://doi.org/10.1002/humu.22225

Mahmoud NA, Ahmed DT, Mohammed ZO, Altyeb FA, Mustafa MI, Hassan MA. The Association between SLC25A15 Gene Polymorphisms and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome: Using in Silico Analysis. bioRxiv. 2019 Sep: 786301. doi: 10.1101/786301. DOI: https://doi.org/10.1101/786301

Kumar P, Henikoff S, Ng PC. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nature Protocols. 2009 Jul; 4(7): 1073-81. doi: 10.1038/nprot.2009.86. DOI: https://doi.org/10.1038/nprot.2009.86

Pires DE, Ascher DB, Blundell TL. mCSM: predicting the effects of mutations in proteins using graph-based signatures. Bioinformatics. 2014 Feb; 30(3): 335-42. doi: 10.1093/bioinformatics/btt691. DOI: https://doi.org/10.1093/bioinformatics/btt691

Emadi E, Akhoundi F, Kalantar SM, Emadi-Baygi M. Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences. BMC Genetics. 2020 Dec; 21(1): 1-27. doi: 10.1186/s12863-020-00890-y. DOI: https://doi.org/10.1186/s12863-020-00890-y

Ashkenazy H, Abadi S, Martz E, Chay O, Mayrose I, Pupko T, et al. ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules. Nucleic Acids Research. 2016 Jul; 44(W1): W344-50. doi: 10.1093/nar/gkw408. DOI: https://doi.org/10.1093/nar/gkw408

Alabid T, Kordofani AA, Atalla B, Altayb HN, Fadla AA, Mohamed M, et al. In silico Analysis of Single Nucleotide Polymorphisms (SNPs) in HumanVCAM-1 gene. Journal of Bioinformatics, Genomics and Proteomics. 2016 May; 1(1): 1004.

Studer G, Tauriello G, Bienert S, Biasini M, Johner N, Schwede T. ProMod3—A versatile homology modelling toolbox. PLoS Computational Biology. 2021 Jan; 17(1): e1008667. doi: 10.1371/journal.pcbi.1008667. DOI: https://doi.org/10.1371/journal.pcbi.1008667

Combet C, Blanchet C, Geourjon C, Deleage G. NPS@: network protein sequence analysis. Trends in Biochemical Sciences. 2000 Mar; 25(3): 147-50. doi: 10.1016/S0968-0004(99)01540-6. DOI: https://doi.org/10.1016/S0968-0004(99)01540-6

Lorenz R, Bernhart SH, Höner zu Siederdissen C, Tafer H, Flamm C, Stadler PF, et al. ViennaRNA Package 2.0. 2011; 6: 1- 14. doi: 10.1186/1748-7188-6-26. DOI: https://doi.org/10.1186/1748-7188-6-26

Gao J, Mazor T, Ciftci E, Raman P, Lukasse P, Bahceci I, et al. The cbioportal for cancer genomics: An intuitive open-source platform for exploration, analysis and visualization of cancer genomics data. Cancer Research. 2018 Jul; 78(13_Supplement): 923-. doi: 10.1158/1538-7445.AM2018-923. DOI: https://doi.org/10.1158/1538-7445.AM2018-923

Chen F, Chandrashekar DS, Varambally S, Creighton CJ. Pan-cancer molecular subtypes revealed by mass-spectrometry-based proteomic characterization of more than 500 human cancers. Nature Communications. 2019 Dec; 10(1): 5679. doi: 10.1038/s41467-019-13528-0. DOI: https://doi.org/10.1038/s41467-019-13528-0

Tang Z, Li C, Kang B, Gao G, Li C, Zhang Z. GEPIA: a web server for cancer and normal gene expression profiling and interactive analyses. Nucleic Acids Research. 2017 Jul; 45(W1): W98-102. doi: 10.1093/nar/gkx247. DOI: https://doi.org/10.1093/nar/gkx247

Zito A, Lualdi M, Granata P, Cocciadiferro D, Novelli A, Alberio T, et al. Gene set enrichment analysis of interaction networks weighted by node centrality. Frontiers in Genetics. 2021 Feb; 12: 577623. doi: 10.3389/fgene.2021.577623. DOI: https://doi.org/10.3389/fgene.2021.577623

Saito R, Smoot ME, Ono K, Ruscheinski J, Wang PL, Lotia S, et al. A travel guide to Cytoscape plugins. Nature Methods. 2012 Nov; 9(11): 1069-76. doi: 10.1038/nmeth.2212. DOI: https://doi.org/10.1038/nmeth.2212

Krebs BB and De Mesquita JF. Amyotrophic lateral sclerosis type 20-In Silico analysis and molecular dynamics simulation of hnRNPA1. PloS One. 2016 Jul; 11(7): e0158939. doi: 10.1371/journal.pone.0158939. DOI: https://doi.org/10.1371/journal.pone.0158939

Yazar M and Özbek P. In Silico Tools and Approaches for the prediction of functional and structural effects of single-nucleotide polymorphisms on proteins: an expert review. OMICS: A Journal of Integrative Biology. 2021 Jan; 25(1): 23-37. doi: 10.1089/omi.2020.0141. DOI: https://doi.org/10.1089/omi.2020.0141

Baird DM. Variation at the TERT locus and predisposition for cancer. Expert Reviews in Molecular Medicine. 2010 May; 12: e16. doi: 10.1017/S146239941000147X. DOI: https://doi.org/10.1017/S146239941000147X

Pak MA, Markhieva KA, Novikova MS, Petrov DS, Vorobyev IS, Maksimova ES, et al. Using AlphaFold to predict the impact of single mutations on protein stability and function. Plos One. 2023 Mar; 18(3): e0282689. doi: 10.1371/journal.pone.0282689. DOI: https://doi.org/10.1371/journal.pone.0282689

Shaw G. Polymorphism and single nucleotide polymorphisms (SNP s). BJU International. 2013 Sep; 112(5): 664-5. doi: 10.1111/bju.12298. DOI: https://doi.org/10.1111/bju.12298

Fung TS and Liu DX. Post-translational modifications of coronavirus proteins: roles and function. Future virology. 2018 May;13(6): 405-30. doi: 10.2217/fvl-2018-0008. DOI: https://doi.org/10.2217/fvl-2018-0008

Simpson CM, Zhang B, Hornbeck PV, Gnad F. Systematic analysis of the intersection of disease mutations with protein modifications. BMC Medical Genomics. 2019 Jul; 12: 1-0. doi: 10.1186/s12920-019-0543-2. DOI: https://doi.org/10.1186/s12920-019-0543-2

Lee DD, Leao R, Komosa M, Gallo M, Zhang CH, Lipman T, et al. DNA hypermethylation within TERT promoter upregulates TERT expression in cancer. The Journal of Clinical Investigation. 2019 Jan; 129(1): 223-9. doi: 10.1172/JCI121303. DOI: https://doi.org/10.1172/JCI121303

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Published

2023-05-31
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DOI: 10.54393/pbmj.v6i05.881
Published: 2023-05-31

How to Cite

Munir, A. ., Akram, A. M. ., Jamil, K. ., & Tahir, A. . (2023). In Silico Post Translational Analysis of Functional Single Nucleotide Alterations in Human TERT Gene Associated with Acute Myeloid Leukemia. Pakistan BioMedical Journal, 6(05), 24–32. https://doi.org/10.54393/pbmj.v6i05.881

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