Cytokine induction of proliferation and expression of CDC2 and cyclin a in FDC‐P1 myeloid hematopoietic progenitor cells: Regulation of ubiquitous and cell cycle‐dependent histone gene transcription factors

To evaluate transcriptional mechanisms during cytokine induction of myeloid progenitor cell proliferation, we examined the expression and activity of transcription factors that control cell cycle‐dependent histone genes in interleukin‐3 (IL‐3)‐dependent FDC‐P1 cells. Histone genes are transcriptionally upregulated in response to a series of cellular regulatory signals that mediate competency for cell cycle progression at the G1/S‐phase transition. We therefore focused on factors that are functionally related to activity of the principal cell cycle progression at the G1/S‐phase transition. We therefore focused on factors that are functionally related to activity of the principal cell cycle regulatory element of the histone H4 promoter:CDC2, cyclin A, as well as RB‐and IRF‐related proteins. Comparisons were made with activities of ubiquitous transcription factors that influence a broad spectrum of promoters independent of proliferation or expression of tissue‐specific phenotypic properties. Northern blot analysis indicates that cellular levels of cyclin A and CDC2 mRNAs increase when DNA synthesis and H4 gene expression are initiated, supporting invoulvement in cell cycle progression. Using gel‐shift assays, incorporating factor‐specific antibody and oligonucleotide competition controls, we define three sequential periods following cytokine stimulation of FDC‐P1 cells when selective upregulation of a subset of transcription factors is observed. In the initial period, the levels of SP1 and HiNF‐P are moderately elevated; ATF, AP‐1, and HiNF‐M/IRF‐2 are maximal during the second period; while E2F and HiNF‐D, which contain cyclin A as a component, predominate during the third period, coinciding with maximal H4 gene expression and DNA synthesis. Differential regulation of H4 gene transcription factors following growth stimulation is consistent with a principal role of histone gene promoter elements in integrating cues from multiple signaling pathways that control cell cycle induction and progression. Regulation of transcription factors controlling histone gene promoter activity within the context of a staged cascade of responsiveness to cyclins and other physiological mediators of proliferation in FDC‐P1 cells provides a paradigm for experimentally addressing interdependent cell cycle and cell growth parameters that are operative in hematopoietic stem cells. © 1995 Wiley‐Liss, Inc.