GSBS Student Publications


Activation of a cell-cycle-regulated histone gene by the oncogenic transcription factor IRF-2

UMMS Affiliation

Graduate School of Biomedical Sciences; Department of Cell Biology



Document Type


Medical Subject Headings

Animals; Base Sequence; Cell Cycle; Cell Line; Cricetinae; DNA; DNA-Binding Proteins; *Gene Expression Regulation; Haplorhini; Hela Cells; Histones; Humans; Interferon Regulatory Factor-1; Interferon Regulatory Factor-2; Molecular Sequence Data; Phosphoproteins; *Repressor Proteins; Transcription Factors; Transcription, Genetic; Transfection


Life Sciences | Medicine and Health Sciences


The human histone H4 gene FO108 is regulated during the cell cycle with a peak in transcription during early S phase. The cell-cycle element (CCE) required for H4 histone activation is a sequence of 11 base pairs that binds a protein factor in electrophoretic mobility shift assays that has been designated histone nuclear factor M (HiNF-M). Here we report the purification of HiNF-M, and show it to be a protein of relative molecular mass (M(r)) 48K that is identical to interferon (IFN) regulatory factor 2 (IRF-2), a negative transcriptional regulator of the IFN response. Recombinant IRF-2 (as well as the related protein IRF-1 (ref. 5)) binds the CCE specifically and activates transcription of this H4 histone gene. IRF-2 has been shown to have oncogenic potential, and our results demonstrate a link between IRF-2 and a gene that is functionally coupled to DNA replication and cell-cycle progression at the G1/S phase transition.

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Citation: Nature. 1995 Sep 28;377(6547):362-5. Link to article on publisher's site

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