The retrotransposon-derived capsid genesPNMA1andPNMA4maintain reproductive capacity

Author:

Wood Thomas W.P.ORCID,Henriques William S.ORCID,Cullen Harrison B.ORCID,Romero MayraORCID,Blengini Cecilia S.ORCID,Sarathy ShreyaORCID,Sorkin JuliaORCID,Bekele HilinaORCID,Jin ChenORCID,Kim SeungsooORCID,Chemiakine Alexei,Khondker Rishad C.ORCID,Isola José V.V.ORCID,Stout Michael B.ORCID,Gennarino Vincenzo A.ORCID,Mogessie BinyamORCID,Jain DevanshiORCID,Schindler KarenORCID,Suh YousinORCID,Wiedenheft BlakeORCID,Berchowitz Luke E.ORCID

Abstract

ABSTRACTThe human genome contains 24gag-like capsid genes derived from deactivated retrotransposons conserved among eutherians. Although some of their encoded proteins retain the ability to form capsids and even transfer cargo, their fitness benefit has remained elusive. Here we show that thegag-like genesPNMA1andPNMA4support reproductive capacity. Six-week-old mice lacking eitherPnma1orPnma4are indistinguishable from wild-type littermates, but by six months the mutant mice become prematurely subfertile, with precipitous drops in sex hormone levels, gonadal atrophy, and abdominal obesity; overall they produce markedly fewer offspring than controls. Analysis of donated human ovaries shows that expression of both genes declines normally with aging, while severalPNMA1andPNMA4variants identified in genome-wide association studies are causally associated with low testosterone, altered puberty onset, or obesity. These findings expand our understanding of factors that maintain human reproductive health and lend insight into the domestication of retrotransposon-derived genes.

Publisher

Cold Spring Harbor Laboratory

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