Evidence map›Paper›PMID 34015158›Full record

ArticleHuman mutation2021

Common polymorphic OTC variants can act as genetic modifiers of enzymatic activity.

Mónica Lopes-Marques, Ana Rita Pacheco, Maria João Peixoto, Ana Rita Cardoso, Catarina Serrano, António Amorim, Maria João Prata, David N Cooper, Luísa Azevedo

Open access · hybridAbstract read
In one paragraph

Article in Human mutation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. International journal of molecular sciences · 2023
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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

9 authors at 3 institutions in 3 countries.

Mónica Lopes-Marquesi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-8597-4730
Ana Rita Pachecoi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-0004-6554
Maria João PeixotoICVS- Life and Health Sciences Research Institute, School of Medicine, University of Minho, Braga, Portugal.ORCID 0000-0002-4739-3409
Ana Rita Cardosoi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0001-5254-5094
Catarina Serranoi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-2390-880X
António Amorimi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-7518-6247
Maria João Pratai3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-0583-1028
David N CooperInstitute of Medical Genetics; School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-8943-8484
Luísa Azevedoi3S-Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-3157-7342
Universidade do Porto · PTUniversity of Minho · PTUniversity of Wales Institute Cardiff · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the role of common polymorphisms in modulating the clinical phenotype when they co-occur with a disease-causing lesion is of critical importance in medical genetics. We explored the impact of apparently neutral common polymorphisms, using the gene encoding the urea cycle enzyme, ornithine transcarbamylase (OTC), as a model system. Distinct combinations of genetic backgrounds embracing two missense polymorphisms were created in cis with the pathogenic p.Arg40His replacement. In vitro enzymatic assays revealed that the polymorphic variants were able to modulate OTC activity both in the presence or absence of the pathogenic lesion. First, we found that the combination of the minor alleles of polymorphisms p.Lys46Arg and p.Gln270Arg significantly enhanced enzymatic activity in the wild-type protein. Second, enzymatic assays revealed that the minor allele of the p.Gln270Arg polymorphism was capable of ameliorating OTC activity when combined in cis with the pathogenic p.Arg40His replacement. Structural analysis predicted that the minor allele of the p.Gln270Arg polymorphism would serve to stabilize the OTC wild-type protein, thereby corroborating the results of the experimental assays. Our findings demonstrate the potential importance of cis-interactions between common polymorphic variants and pathogenic missense mutations and illustrate how standing genetic variation can modulate protein function.

Indexed as

Ornithine CarbamoyltransferaseOrnithine Carbamoyltransferase Deficiency DiseaseAllelesHumansMutation, MissensePolymorphism, GeneticOrnithine CarbamoyltransferaseOTC protein, humanenzymatic activitygenetic modifiersOTC genepathogenic replacementspolymorphic variantsstructural modeling

Identifiers

PMID34015158
PMCPMC8362079
OpenAlexW3162372980

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.