Abstract
The human histone H3.3B gene belongs to the group of replacement histone genes, which are up-regulated during differentiation of cells. Here we provide evidence that a cAMP response element/PMA response element (CRE/TRE) located in the proximal promoter contributes to the expression of the H3.3B gene. (1) Band shift and supershift analysis demonstrated the binding of AP-1 and transcription factors of the CRE-binding protein/activating-transcription-factor family to the H3.3B CRE/TRE. (2) Treatment of HeLa cells with PMA led to a 4-fold increase in H3. 3B mRNA levels within 2 h, whereas transcription of the cell cycle-dependent H3 histone genes remained constant. In contrast with PMA, cAMP did not affect H3.3B transcription. (3) PMA treatment of cells transiently transfected with H3.3B promoter constructs linked to a luciferase gene caused a 4-5-fold increase in reporter gene activity, whereas mutation of the CRE/TRE element abolished the PMA response. These results demonstrate that activation of the protein kinase C pathway by PMA results in an early up-regulation of H3.3B gene expression via the CRE/TRE element. Furthermore treatment with PMA apparently leads to differential induction of H3 histone subtype genes and this in turn can result in a remodelling of chromatin structure of cells before or during differentiation processes.
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- Albig W., Bramlage B., Gruber K., Klobeck H. G., Kunz J., Doenecke D. The human replacement histone H3.3B gene (H3F3B). Genomics. 1995 Nov 20;30(2):264–272. doi: 10.1006/geno.1995.9878. [DOI] [PubMed] [Google Scholar]
- Albig W., Drabent B., Kunz J., Kalff-Suske M., Grzeschik K. H., Doenecke D. All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6. Genomics. 1993 Jun;16(3):649–654. doi: 10.1006/geno.1993.1243. [DOI] [PubMed] [Google Scholar]
- Albig W., Kioschis P., Poustka A., Meergans K., Doenecke D. Human histone gene organization: nonregular arrangement within a large cluster. Genomics. 1997 Mar 1;40(2):314–322. doi: 10.1006/geno.1996.4592. [DOI] [PubMed] [Google Scholar]
- Allen B. S., Stein J. L., Stein G. S., Ostrer H. Single-copy flanking sequences in human histone gene clusters map to chromosomes 1 and 6. Genomics. 1991 Jun;10(2):486–488. doi: 10.1016/0888-7543(91)90337-e. [DOI] [PubMed] [Google Scholar]
- Angel P., Hattori K., Smeal T., Karin M. The jun proto-oncogene is positively autoregulated by its product, Jun/AP-1. Cell. 1988 Dec 2;55(5):875–885. doi: 10.1016/0092-8674(88)90143-2. [DOI] [PubMed] [Google Scholar]
- Bramlage B., Kosciessa U., Doenecke D. Differential expression of the murine histone genes H3.3A and H3.3B. Differentiation. 1997 Oct;62(1):13–20. doi: 10.1046/j.1432-0436.1997.6210013.x. [DOI] [PubMed] [Google Scholar]
- Brush D., Dodgson J. B., Choi O. R., Stevens P. W., Engel J. D. Replacement variant histone genes contain intervening sequences. Mol Cell Biol. 1985 Jun;5(6):1307–1317. doi: 10.1128/mcb.5.6.1307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Castiglia D., Cestelli A., Scaturro M., Nastasi T., Di Liegro I. H1(0) and H3.3B mRNA levels in developing rat brain. Neurochem Res. 1994 Dec;19(12):1531–1537. doi: 10.1007/BF00969002. [DOI] [PubMed] [Google Scholar]
- Chirgwin J. M., Przybyla A. E., MacDonald R. J., Rutter W. J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 1979 Nov 27;18(24):5294–5299. doi: 10.1021/bi00591a005. [DOI] [PubMed] [Google Scholar]
- Dignam J. D., Martin P. L., Shastry B. S., Roeder R. G. Eukaryotic gene transcription with purified components. Methods Enzymol. 1983;101:582–598. doi: 10.1016/0076-6879(83)01039-3. [DOI] [PubMed] [Google Scholar]
- Doenecke D., Albig W., Bode C., Drabent B., Franke K., Gavenis K., Witt O. Histones: genetic diversity and tissue-specific gene expression. Histochem Cell Biol. 1997 Jan;107(1):1–10. doi: 10.1007/s004180050083. [DOI] [PubMed] [Google Scholar]
- Gabrielli F., Aden D. P., Carrel S. C., von Bahr C., Rane A., Angeletti C. A., Hancock R. Histone complements of human tissues, carcinomas, and carcinoma-derived cell lines. Mol Cell Biochem. 1984 Nov;65(1):57–66. [PubMed] [Google Scholar]
- Hurst H. C., Totty N. F., Jones N. C. Identification and functional characterisation of the cellular activating transcription factor 43 (ATF-43) protein. Nucleic Acids Res. 1991 Sep 11;19(17):4601–4609. doi: 10.1093/nar/19.17.4601. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Karin M., Smeal T. Control of transcription factors by signal transduction pathways: the beginning of the end. Trends Biochem Sci. 1992 Oct;17(10):418–422. doi: 10.1016/0968-0004(92)90012-x. [DOI] [PubMed] [Google Scholar]
- Krimer D. B., Cheng G., Skoultchi A. I. Induction of H3.3 replacement histone mRNAs during the precommitment period of murine erythroleukemia cell differentiation. Nucleic Acids Res. 1993 Jun 25;21(12):2873–2879. doi: 10.1093/nar/21.12.2873. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pantazis P., Bonner W. M. Specific alterations in the pattern of histone-3 synthesis during conversion of human leukemic cells to terminally differentiated cells in culture. Differentiation. 1984;28(2):186–190. doi: 10.1111/j.1432-0436.1984.tb00282.x. [DOI] [PubMed] [Google Scholar]
- Pauli U., Chrysogelos S., Nick H., Stein G., Stein J. In vivo protein binding sites and nuclease hypersensitivity in the promoter region of a cell cycle regulated human H3 histone gene. Nucleic Acids Res. 1989 Mar 25;17(6):2333–2350. doi: 10.1093/nar/17.6.2333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfeffer L. M., Strulovici B., Saltiel A. R. Interferon-alpha selectively activates the beta isoform of protein kinase C through phosphatidylcholine hydrolysis. Proc Natl Acad Sci U S A. 1990 Sep;87(17):6537–6541. doi: 10.1073/pnas.87.17.6537. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roesler W. J., Vandenbark G. R., Hanson R. W. Cyclic AMP and the induction of eukaryotic gene transcription. J Biol Chem. 1988 Jul 5;263(19):9063–9066. [PubMed] [Google Scholar]
- Sharma A., Bos T. J., Pekkala-Flagan A., Vogt P. K., Lee A. S. Interaction of cellular factors related to the Jun oncoprotein with the promoter of a replication-dependent hamster histone H3.2 gene. Proc Natl Acad Sci U S A. 1989 Jan;86(2):491–495. doi: 10.1073/pnas.86.2.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thoma F., Koller T., Klug A. Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin. J Cell Biol. 1979 Nov;83(2 Pt 1):403–427. doi: 10.1083/jcb.83.2.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wells D., Hoffman D., Kedes L. Unusual structure, evolutionary conservation of non-coding sequences and numerous pseudogenes characterize the human H3.3 histone multigene family. Nucleic Acids Res. 1987 Apr 10;15(7):2871–2889. doi: 10.1093/nar/15.7.2871. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Witt O., Albig W., Doenecke D. Testis-specific expression of a novel human H3 histone gene. Exp Cell Res. 1996 Dec 15;229(2):301–306. doi: 10.1006/excr.1996.0375. [DOI] [PubMed] [Google Scholar]
- Witt O., Albig W., Doenecke D. Transcriptional regulation of the human replacement histone gene H3.3B. FEBS Lett. 1997 May 26;408(3):255–260. doi: 10.1016/s0014-5793(97)00436-5. [DOI] [PubMed] [Google Scholar]
- Wu R. S., Bonner W. M. Separation of basal histone synthesis from S-phase histone synthesis in dividing cells. Cell. 1981 Dec;27(2 Pt 1):321–330. doi: 10.1016/0092-8674(81)90415-3. [DOI] [PubMed] [Google Scholar]
- Wu R. S., Perry L. J., Bonner W. M. Fate of newly synthesized histones in G1 and G0 cells. FEBS Lett. 1983 Oct 3;162(1):161–166. doi: 10.1016/0014-5793(83)81070-9. [DOI] [PubMed] [Google Scholar]
- Wu R. S., Tsai S., Bonner W. M. Changes in histone H3 composition and synthesis pattern during lymphocyte activation. Biochemistry. 1983 Aug 2;22(16):3868–3873. doi: 10.1021/bi00285a023. [DOI] [PubMed] [Google Scholar]
- Wu R. S., Tsai S., Bonner W. M. Patterns of histone variant synthesis can distinguish G0 from G1 cells. Cell. 1982 Dec;31(2 Pt 1):367–374. doi: 10.1016/0092-8674(82)90130-1. [DOI] [PubMed] [Google Scholar]
- van Wijnen A. J., Lian J. B., Stein J. L., Stein G. S. Protein/DNA interactions involving ATF/AP1-, CCAAT-, and HiNF-D-related factors in the human H3-ST519 histone promoter: cross-competition with transcription regulatory sites in cell cycle controlled H4 and H1 histone genes. J Cell Biochem. 1991 Dec;47(4):337–351. doi: 10.1002/jcb.240470408. [DOI] [PubMed] [Google Scholar]