Evidence map›Paper›PMID 34173867›Full record

ArticleHuman genetics2021

Compensatory epistasis explored by molecular dynamics simulations.

Catarina Serrano, Carla S S Teixeira, David N Cooper, João Carneiro, Mónica Lopes-Marques, Peter D Stenson, António Amorim, Maria J Prata, Sérgio F Sousa, Luísa Azevedo

Abstract read
PubMed Publisher
In one paragraph

Article in Human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
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

10 authors at 2 institutions in 2 countries.

Catarina Serranoi3S, Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Carla S S TeixeiraUCIBIO/REQUIMTE, BioSIM, Departamento de Biomedicina, Faculdade de Medicina da Universidade do Porto, Porto, Portugal.
David N CooperInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, CF14 4XN, UK.
João CarneiroCIIMAR, Interdisciplinary Centre of Marine and Environmental Research, Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos, s/n, 4450-208, Matosinhos, Portugal.
Mónica Lopes-Marquesi3S, Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Peter D StensonInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, CF14 4XN, UK.
António Amorimi3S, Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Maria J Pratai3S, Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Sérgio F Sousa *UCIBIO/REQUIMTE, BioSIM, Departamento de Biomedicina, Faculdade de Medicina da Universidade do Porto, Porto, Portugal. sergiofsousa@med.up.pt.
Luísa Azevedo *i3S, Instituto de Investigação e Inovação em Saúde, Population Genetics and Evolution Group, Universidade do Porto, Rua Alfredo Allen 208, 4200-135, Porto, Portugal. lazevedo@ipatimup.pt.ORCID http://orcid.org/0000-0002-3157-7342
Universidade do Porto · PTCardiff University · GB

Funding

Foundation for Science and Technology 01/SAICT/2016 number 022153Foundation for Science and Technology 2020.01423.CEECINDFoundation for Science and Technology CPCA/A00/7140/2020Foundation for Science and Technology CPCA/A00/7145/2020Foundation for Science and Technology POCI-01-0145-FEDER-007274Foundation for Science and Technology POCI-01-0145-FEDER-29723Foundation for Science and Technology SFRH/BD/137925/2018Foundation for Science and Technology UIDB/04378/2020Foundation for Science and Technology UIDB/04423/2020Foundation for Science and Technology UIDP/04378/2020Foundation for Science and Technology UIDP/04423/2020
6 · The paper itself

Abstract

A non-negligible proportion of human pathogenic variants are known to be present as wild type in at least some non-human mammalian species. The standard explanation for this finding is that molecular mechanisms of compensatory epistasis can alleviate the mutations' otherwise pathogenic effects. Examples of compensated variants have been described in the literature but the interacting residue(s) postulated to play a compensatory role have rarely been ascertained. In this study, the examination of five human X-chromosomally encoded proteins (FIX, GLA, HPRT1, NDP and OTC) allowed us to identify several candidate compensated variants. Strong evidence for a compensated/compensatory pair of amino acids in the coagulation FIXa protein (involving residues 270 and 271) was found in a variety of mammalian species. Both amino acid residues are located within the 60-loop, spatially close to the 39-loop that performs a key role in coagulation serine proteases. To understand the nature of the underlying interactions, molecular dynamics simulations were performed. The predicted conformational change in the 39-loop consequent to the Glu270Lys substitution (associated with hemophilia B) appears to impair the protein's interaction with its substrate but, importantly, such steric hindrance is largely mitigated in those proteins that carry the compensatory residue (Pro271) at the neighboring amino acid position.

Indexed as

Epistasis, GeneticFactor IXaMolecular Dynamics SimulationMutation, MissenseAmino Acid SubstitutionChromosomes, Human, XHumansFactor IXa

Identifiers

PMID34173867
OpenAlexW3173577086

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.