2020Proceedings of the National Academy of SciencesOpen access

Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes

Antonio Rausell, Yufei Luo, Marie Lopez, Yoann Seeleuthner, Franck Rapaport, Antoine Favier, Peter D. Stenson, D.N. Cooper, Étienne Patin, Jean‐Laurent Casanova, Lluís Quintana‐Murci, Laurent Abel

Open full text 43 citations

Abstract

Significance Human genes homozygous for apparent loss of function (LoF) variants are increasingly reported in a sizeable proportion of individuals without overt clinical phenotypes. Here, we found 166 genes with 179 predicted LoF variants for which the frequency of homozygous individuals exceeds 1% in at least one of the populations present in databases ExAC and gnomAD. These putatively dispensable genes showed relaxation of selective constraints, suggesting that a considerable proportion of these genes may be undergoing pseudogenization. Eight of these LoF variants displayed robust signals of positive selection, including two variants in genes involved in resistance to infectious diseases. The identification of dispensable genes will facilitate the identification of functions that are now redundant, or possibly even advantageous, for human survival.

About this research paper

What this paper is about

Significance Human genes homozygous for apparent loss of function (LoF) variants are increasingly reported in a sizeable proportion of individuals without overt clinical phenotypes. Here, we found 166 genes with 179 predicted LoF variants for which the frequency of homozygous individuals exceeds 1% in at least one of the populations present in databases ExAC and gnomAD. These putatively dispensable genes showed relaxation of selective constraints, suggesting that a considerable proportion of these genes may be undergoing pseudogenization. Eight of these LoF variants displayed robust signals of positive selection, including two variants in genes involved in resistance to infectious diseases. The identification of dispensable genes will facilitate the identification of functions that are now redundant, or possibly even advantageous, for human survival.

Why it matters

OpenAlex reports 43 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Significance Human genes homozygous for apparent loss of function (LoF) variants are increasingly reported in a sizeable proportion of individuals without overt clinical phenotypes. Here, we found 166 genes with 179 predicted LoF variants for which the frequency of homozygous individuals exceeds 1% in at least one of the populations present in databases ExAC and gnomAD. These putatively dispensable genes showed relaxation of selective constraints, suggesting that a considerable proportion of these genes may be undergoing pseudogenization. Eight of these LoF variants displayed robust signals of positive selection, including two variants in genes involved in resistance to infectious diseases. The identification of dispensable genes will facilitate the identification of functions that are now redundant, or possibly even advantageous, for human survival.

Key concepts: Gene, Genetics, Biology, Phenotype, Loss function, Function (biology), Identification (biology), Botany

Related papers

Back to paper searchBrowse research topicsOriginal source
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes — Research Paper | ScholarLens