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Gv1, a Zinc Finger Gene Controlling Endogenous MLV Expression
Author(s) -
George R. Young,
Aaron Ferron,
Veera Panova,
Urszula Eksmond,
Peter L. Oliver,
George Kassiotis,
Jonathan P. Stoye
Publication year - 2021
Publication title -
molecular biology and evolution
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.637
H-Index - 218
eISSN - 1537-1719
pISSN - 0737-4038
DOI - 10.1093/molbev/msab039
Subject(s) - biology , endogenous retrovirus , endogeny , gene , genetics , zinc finger , murine leukemia virus , locus (genetics) , phenotype , epigenetics , allele , chromatin , genome , transcription factor , endocrinology
The genomes of inbred mice harbor around 50 endogenous murine leukemia virus (MLV) loci, although the specific complement varies greatly between strains. The Gv1 locus is known to control the transcription of endogenous MLVs and to be the dominant determinant of cell-surface presentation of MLV envelope, the GIX antigen. Here, we identify a single Krüppel-associated box zinc finger protein (ZFP) gene, Zfp998, as Gv1 and show it to be necessary and sufficient to determine the GIX+ phenotype. By long-read sequencing of bacterial artificial chromosome clones from 129 mice, the prototypic GIX+ strain, we reveal the source of sufficiency and deficiency as splice-acceptor variations and highlight the varying origins of the chromosomal region encompassing Gv1. Zfp998 becomes the second identified ZFP gene responsible for epigenetic suppression of endogenous MLVs in mice and further highlights the prominent role of this gene family in control of endogenous retroviruses.

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