Transcription of Histone H4, H3, and H1 Cell Cycle Genes: Promoter Factor HiNF-D Contains CDC2, Cyclin A, and an RB-Related Protein

Cell cycle-controlled human histone genes are coordinately expressed during S phase, and transcriptional regulation involves a series of trans-acting factors (HiNFs). The proliferation-specific factor HiNF-D interacts with multiple recognition motifs in histone H4, H3, and H1 promoters. Using gel sh...

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Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 91; no. 26; pp. 12882 - 12886
Main Authors: van Wijnen, Andre J., Aziz, Farah, Grana, Xavier, De Luca, Antonio, Desai, Rajesh K., Jaarsveld, Karen, Last, Thomas J., Soprano, Kenneth, Giordano, Antonio, Lian, Jane B., Stein, Janet L., Stein, Gary S.
Format: Journal Article
Language:English
Published: United States National Academy of the Sciences of the United States of America 20-12-1994
National Acad Sciences
National Academy of Sciences
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Summary:Cell cycle-controlled human histone genes are coordinately expressed during S phase, and transcriptional regulation involves a series of trans-acting factors (HiNFs). The proliferation-specific factor HiNF-D interacts with multiple recognition motifs in histone H4, H3, and H1 promoters. Using gel shift immunoassays, we show that CDC2, cyclin A, and an RB-related protein are ubiquitous subunits of HiNF-D binding activity isolated from several cell types. HiNF-D levels in vivo are sensitive to okadaic acid and staurosporine, indicating that HiNF-D activity and/or assembly is influenced by phosphorylation status. Thus, HiNF-D appears to be a multicomponent phosphoprotein that participates in coordinate control of multiple histone H4, H3, and H1 genes during the cell cycle. The presence of cell cycle mediators in the HiNF-D complex suggests linkage between transcriptional control of histones, enzymes involved in DNA synthesis, and the onset of DNA replication during the G1/S phase transition.
Bibliography:ObjectType-Article-2
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content type line 23
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.91.26.12882