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) |
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 |
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 |