Virus Details


VHFID6653

Host Factor Information

Gene Name Gmeb2
HF Protein Name Glucocorticoid modulatory element-binding protein 2
HF Function PIF p79 activates the NS1 nickase function
Uniprot ID P58929
Protein Sequence View Fasta Sequence
NCBI Gene ID 229004
Host Factor (HF) Name in Paper Gmeb2
Gene synonyms N.A.
Ensemble Gene ID ENSMUSG00000038705
Ensemble Transcript ENSMUST00000049032
KEGG ID Go to KEGG Database
Gene Ontology ID(s) GO:0000978, GO:0003713, GO:0005634, GO:0005654, GO:0005829, GO:0006351, GO:0006357, GO:0046872,
MINT ID P58929
STRING Click to see interaction map
GWAS Analysis Click to see gwas analysis
OMIM ID N.A.
PANTHER ID PTHR10417
PDB ID(s) N.A.,
pfam ID PF01342,
Drug Bank ID N.A.,
ChEMBL ID N.A.
Organism Mus musculus (Mouse)

Pathogen Information

Virus Name Mice minute virus
Virus Short Name MMV
Order Unassigned
Virus Family Parvoviridae
Virus Subfamily Parvovirinae
Genus Protoparvovirus
Species Mice minute virus
Host Vertebrates
Cell Tropism Mice minute virus p & i: fibroblasts & lymphocytes
Associated Disease Gastrointestinal tract damage
Mode of Transmission Respiratory, oral droplets of fecal oral-route
VIPR DB link N.A.
ICTV DB link https://talk.ictvonline.org/ictv-reports/ictv_9th_report/ssdna-viruses-2011/w/ssdna_viruses/151/parvoviridae
Virus Host DB link http://www.genome.jp/virushostdb/view/?virus_lineage=Parvoviridae

Publication Information

Paper Title Minute virus of mice initiator protein NS1 and a host KDWK family transcription factor must form a precise ternary complex with origin DNA for nicking to occur
Author's Name Jesper Christensen, Susan F. Cotmore, and Peter Tattersall
Journal Name Journal Of Virology
Pubmed ID 11435581
Abstract Parvoviral rolling hairpin replication generates palindromic genomic concatemers whose junctions are resolved to give unit-length genomes by a process involving DNA replication initiated at origins derived from each viral telomere. The left-end origin of minute virus of mice (MVM), oriL, contains binding sites for the viral initiator nickase, NS1, and parvovirus initiation factor (PIF), a member of the emerging KDWK family of transcription factors. oriL is generated as an active form, oriL(TC), and as an inactive form, oriL(GAA), which contains a single additional nucleotide inserted between the NS1 and PIF sites. Here we examined the interactions on oriL(TC) which lead to activation of NS1 by PIF. The two subunits of PIF, p79 and p96, cooperatively bind two ACGT half-sites, which can be flexibly spaced. When coexpressed from recombinant baculoviruses, the PIF subunits preferentially form heterodimers which, in the presence of ATP, show cooperative binding with NS1 on oriL, but this interaction is preferentially enhanced on oriL(TC) compared to oriL(GAA). Without ATP, NS1 is unable to bind stably to its cognate site, but PIF facilitates this interaction, rendering the NS1 binding site, but not the nick site, resistant to DNase I. Varying the spacing of the PIF half-sites shows that the distance between the NS1 binding site and the NS1-proximal half-site is critical for nickase activation, whereas the position of the distal half-site is unimportant. When expressed separately, both PIF subunits form homodimers that bind site specifically to oriL, but only complexes containing p79 activate the NS1 nickase function.
Used Model HeLa cells
DOI 10.1128/JVI.75.15.7009-7017.2001