Evidence map›Paper›PMID 28410371›Full record

ArticlePloS one2017

Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.

Sneha P, Thirumal Kumar D, George Priya Doss C, Siva R, Hatem Zayed

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Chinese carrier of theHeliyon · 2024
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  7. Article
  8. Article
  9. HNF1A Mutations and Beta Cell Dysfunction in Diabetes.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. In Silico Analysis of Coding/Noncoding SNPs of HumanJournal of diabetes research · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Sneha PSchool of BioSciences and Technology,Vellore Institute of Technology, Vellore, Tamil Nadu, India.
Thirumal Kumar DSchool of BioSciences and Technology,Vellore Institute of Technology, Vellore, Tamil Nadu, India.
George Priya Doss CSchool of BioSciences and Technology,Vellore Institute of Technology, Vellore, Tamil Nadu, India.
Siva RSchool of BioSciences and Technology,Vellore Institute of Technology, Vellore, Tamil Nadu, India.
Hatem ZayedDepartment of Biomedical Sciences, College of Health Sciences, Qatar University, Doha, Qatar.
Vellore Institute of Technology University · INQatar University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maturity-onset diabetes of the young type 3 (MODY3) is a non-ketotic form of diabetes associated with poor insulin secretion. Over the past years, several studies have reported the association of missense mutations in the Hepatocyte Nuclear Factor 1 Alpha (HNF1A) with MODY3. Missense mutations in the POU homeodomain (POUH) of HNF1A hinder binding to the DNA, thereby leading to a dysfunctional protein. Missense mutations of the HNF1A were retrieved from public databases and subjected to a three-step computational mutational analysis to identify the underlying mechanism. First, the pathogenicity and stability of the mutations were analyzed to determine whether they alter protein structure and function. Second, the sequence conservation and DNA-binding sites of the mutant positions were assessed; as HNF1A protein is a transcription factor. Finally, the biochemical properties of the biological system were validated using molecular dynamic simulations in Gromacs 4.6.3 package. Two arginine residues (131 and 203) in the HNF1A protein are highly conserved residues and contribute to the function of the protein. Furthermore, the R131W, R131Q, and R203C mutations were predicted to be highly deleterious by in silico tools and showed lower binding affinity with DNA when compared to the native protein using the molecular docking analysis. Triplicate runs of molecular dynamic (MD) simulations (50ns) revealed smaller changes in patterns of deviation, fluctuation, and compactness, in complexes containing the R131Q and R131W mutations, compared to complexes containing the R203C mutant complex. We observed reduction in the number of intermolecular hydrogen bonds, compactness, and electrostatic potential, as well as the loss of salt bridges, in the R203C mutant complex. Substitution of arginine with cysteine at position 203 decreases the affinity of the protein for DNA, thereby destabilizing the protein. Based on our current findings, the MD approach is an important tool for elucidating the impact and affinity of mutations in DNA-protein interactions and understanding their function.

Indexed as

Mutation, MissenseAmino Acid SequenceBinding SitesDiabetes Mellitus, Type 2DNAHepatocyte Nuclear Factor 1-alphaHumansHydrogen BondingHydrophobic and Hydrophilic InteractionsMolecular Docking SimulationMutagenesis, Site-DirectedPrincipal Component AnalysisProtein BindingProtein DomainsProtein StabilityRecombinant ProteinsDNAHepatocyte Nuclear Factor 1-alphaRecombinant Proteins

Identifiers

PMID28410371
PMCPMC5391926
OpenAlexW2606263411

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.