Evidence map›Paper›PMID 38802968›Full record

ArticleHuman genomics2024

Evolutionary and functional analyses of LRP5 in archaic and extant modern humans.

Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natàlia Garcia-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg and 1 more

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Article in Human genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors.

Neus Roca-AyatsDepartament de Genètica, Microbiologia i Estadística and IBUB, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-3898-7088
Iago MacedaCNAG, Centre Nacional d'Analisi Genòmic, C/ Baldiri I Reixach 4, 08028, Barcelona, Spain.ORCID 0000-0002-9494-6184
Carlos David BruqueUnidad de Conocimiento Traslacional Hospitalaria Patagónica, Hospital de Alta Complejidad El Calafate - S.A.M.I.C., Santa Cruz, Argentina.ORCID 0000-0003-0726-5418
Núria Martínez-GilDepartament de Genètica, Microbiologia i Estadística and IBUB, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-9987-2858
Natàlia Garcia-GiraltMusculoskeletal Research Group, IMIM (Hospital del Mar Medical Research Institute), Centro de Investigación Biomédica en Red en Fragilidad y Envejecimiento Saludable (CIBERFES), ISCIII, Departament de Genètica, Microbiologia i Estadística, UB, Barcelona, Spain.ORCID 0000-0001-6507-0147
Mónica CozarDepartament de Genètica, Microbiologia i Estadística and IBUB, Universitat de Barcelona, Barcelona, Spain.
Leonardo MellibovskyMusculoskeletal Research Group, IMIM (Hospital del Mar Medical Research Institute), Centro de Investigación Biomédica en Red en Fragilidad y Envejecimiento Saludable (CIBERFES), ISCIII, Barcelona, Spain.ORCID 0009-0001-7921-8840
Wim Van HulCenter of Medical Genetics, University of Antwerp, 2650, Antwerp, Belgium.ORCID 0000-0002-5065-7858
Oscar Lao *Institute of Evolutionary Biology, CSIC-Universitat Pompeu Fabra, 08003, Barcelona, Spain. oscar.lao@ibe.upf-csic.es.ORCID 0000-0002-8525-9649
Daniel Grinberg *Departament de Genètica, Microbiologia i Estadística and IBUB, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0001-9859-2590
Susanna Balcells *Departament de Genètica, Microbiologia i Estadística and IBUB, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0003-1211-1907

Funding

Catalan Government 2017SGR:00738Generalitat de Catalunya GRC 2017 SGR 937Ministerio de Ciencia e Innovación SAF 2016-75948R and PID2019-107188RB-C21Ministerio de Economía y Competitividad PGC2018-098574-B-I00
6 · The paper itself

Abstract

backgroundThe human lineage has undergone a postcranial skeleton gracilization (i.e. lower bone mass and strength relative to body size) compared to other primates and archaic populations such as the Neanderthals. This gracilization has been traditionally explained by differences in the mechanical load that our ancestors exercised. However, there is growing evidence that gracilization could also be genetically influenced.

resultsWe have analyzed the LRP5 gene, which is known to be associated with high bone mineral density conditions, from an evolutionary and functional point of view. Taking advantage of the published genomes of archaic Homo populations, our results suggest that this gene has a complex evolutionary history both between archaic and living humans and within living human populations. In particular, we identified the presence of different selective pressures in archaics and extant modern humans, as well as evidence of positive selection in the African and South East Asian populations from the 1000 Genomes Project. Furthermore, we observed a very limited evidence of archaic introgression in this gene (only at three haplotypes of East Asian ancestry out of the 1000 Genomes), compatible with a general erasing of the fingerprint of archaic introgression due to functional differences in archaics compared to extant modern humans. In agreement with this hypothesis, we observed private mutations in the archaic genomes that we experimentally validated as putatively increasing bone mineral density. In particular, four of five archaic missense mutations affecting the first β-propeller of LRP5 displayed enhanced Wnt pathway activation, of which two also displayed reduced negative regulation.

conclusionsIn summary, these data suggest a genetic component contributing to the understanding of skeletal differences between extant modern humans and archaic Homo populations.

Indexed as

Evolution, MolecularLow Density Lipoprotein Receptor-Related Protein-5NeanderthalsAnimalsBone DensityGenome, HumanHaplotypesHominidaeHumansSelection, GeneticLow Density Lipoprotein Receptor-Related Protein-5LRP5 protein, humanArchaic introgressionBone mineral densityDenisovanHuman evolutionLRP5Neanderthal

Identifiers

PMID38802968
PMCPMC11131306

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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.