In Silico Functional and Structural Analysis of Non-synonymous Single Nucleotide Polymorphisms (nsSNPs) in Human Paired Box 4 Gene
- PMID: 38062275
- DOI: 10.1007/s10528-023-10589-1
In Silico Functional and Structural Analysis of Non-synonymous Single Nucleotide Polymorphisms (nsSNPs) in Human Paired Box 4 Gene
Abstract
In human genome, members of Paired box (PAX) transcription factor family are highly sequence-specific DNA-binding proteins. Among PAX gene family members, PAX4 gene has significant role in growth, proliferation, differentiation, and insulin secretion of pancreatic β-cells. Single nucleotide polymorphisms (SNPs) in PAX4 gene progress in the pathogenesis of various human diseases. Hence, the molecular mechanism of how these SNPs in PAX4 gene significantly progress diseases pathogenesis needs to be elucidated. For the reason, a series of bioinformatic analyzes were done to identify the SNPs of PAX4 gene that contribute in diseases pathogenesis. From the analyzes, 4145 SNPs (rsIDs) in PAX4 gene were obtained, where, 362 missense (8.73%), 169 synonymous (4.08%), and 2323 intron variants (56.04%). The rest SNPs were unspecified. Among the 362 missense variants, 118 nsSNPs were found as deleterious in SIFT analysis. Among those, 25 nsSNPs were most probably damaging and 23 were deleterious as observed in PolyPhen-2 and PROVEAN analyzes, respectively. Following all analyzes, 14 nsSNPs (rs149708455, rs115887120, rs147279315, rs35155575, rs370095957, rs373939873, rs145468905, rs121917718, rs2233580, rs3824004, rs372751660, rs369459316, rs375472849, rs372497946) were common and observed as deleterious, probably damaging, affective and diseases associated. Following structural analyzes, 11 nsSNPs guided proteins were found as most unstable and highly conserved. Among these, R20W, R39Q, R45Q, R60H, G65D, and A223D mutated proteins were highly harmful. Hence, the results from above-mentioned integrated comprehensive bioinformatic analyzes guide how different nsSNPs in PAX4 gene alter structural and functional characteristics of the protein that might progress diseases pathogenesis in human including type 2 diabetes.
Keywords: Paired box 4; Protein characteristics; Single nucleotide polymorphisms.
© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Similar articles
-
Investigating the functional and structural effect of non-synonymous single nucleotide polymorphisms in the cytotoxic T-lymphocyte antigen-4 gene: An in-silico study.PLoS One. 2025 Jan 24;20(1):e0316465. doi: 10.1371/journal.pone.0316465. eCollection 2025. PLoS One. 2025. PMID: 39854591 Free PMC article.
-
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 Genet. 2020 Aug 31;21(1):94. doi: 10.1186/s12863-020-00890-y. BMC Genet. 2020. PMID: 32867672 Free PMC article.
-
Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.Diabetologia. 2017 Jan;60(1):107-115. doi: 10.1007/s00125-016-4132-z. Epub 2016 Oct 15. Diabetologia. 2017. PMID: 27744525
-
Screening and insilico analysis of deleterious nsSNPs (missense) in human CSF3 for their effects on protein structure, stability and function.Comput Biol Chem. 2019 Oct;82:57-64. doi: 10.1016/j.compbiolchem.2019.06.001. Epub 2019 Jun 6. Comput Biol Chem. 2019. PMID: 31272062
-
Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.Neuroscience. 2007 Apr 14;145(4):1273-9. doi: 10.1016/j.neuroscience.2006.09.004. Epub 2006 Oct 19. Neuroscience. 2007. PMID: 17055652 Review.
Cited by
-
In silico functional, structural and pathogenicity analysis of missense single nucleotide polymorphisms in human MCM6 gene.Sci Rep. 2024 May 21;14(1):11607. doi: 10.1038/s41598-024-62299-2. Sci Rep. 2024. PMID: 38773180 Free PMC article.
-
Prediction and assessment of deleterious and disease causing nonsynonymous single nucleotide polymorphisms (nsSNPs) in human FOXP4 gene: An in - silico study.Heliyon. 2024 Jun 15;10(12):e32791. doi: 10.1016/j.heliyon.2024.e32791. eCollection 2024 Jun 30. Heliyon. 2024. PMID: 38994097 Free PMC article.
-
Investigating the functional and structural effect of non-synonymous single nucleotide polymorphisms in the cytotoxic T-lymphocyte antigen-4 gene: An in-silico study.PLoS One. 2025 Jan 24;20(1):e0316465. doi: 10.1371/journal.pone.0316465. eCollection 2025. PLoS One. 2025. PMID: 39854591 Free PMC article.
References
-
- Acharya C, Yik JHN, Kishore A, Van Dinh V, Di Cesare PE, Haudenschild DR (2014) Cartilage oligomeric matrix protein and its binding partners in the cartilage extracellular matrix: interaction, regulation and role in chondrogenesis. Matrix Biol 37:102–111. https://doi.org/10.1016/j.matbio.2014.06.001 - DOI - PubMed
-
- Adzhubei I, Jordan DM, Sunyaev SR (2013) Predicting functional effect of human missense mutations using PolyPhen-2. Curr Protoc Hum Genet 76:7–20. https://doi.org/10.1002/0471142905.hg0720s76 - DOI
-
- Ahmad T, Valentovic MA, Rankin GO (2018) Effects of cytochrome P450 single nucleotide polymorphisms on methadone metabolism and pharmacodynamics. Biochem Pharmacol 153:196–204. https://doi.org/10.1016/j.bcp.2018.02.020 - DOI - PubMed - PMC
-
- Ahmed SS, Rifat ZT, Lohia R, Campbell AJ, Dunker AK, Rahman MS, Iqbal S (2022) Characterization of intrinsically disordered regions in proteins informed by human genetic diversity. Plos Comput Biol 18(3):e1009911. https://doi.org/10.1371/journal.pcbi.1009911 - DOI - PubMed - PMC
-
- Anik A, Çatli G, Abaci A, Böber E (2015) Maturity-onset diabetes of the young (MODY): an update. J Pediatr Endocrinol Metab 28:251–263. https://doi.org/10.1515/jpem-2014-0384 - DOI - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources