Skip to main content
Molecular and Cellular Biology logoLink to Molecular and Cellular Biology
. 1996 May;16(5):1936–1945. doi: 10.1128/mcb.16.5.1936

Role of the liver-enriched transcription factor hepatocyte nuclear factor 1 in transcriptional regulation of the factor V111 gene.

L K McGlynn 1, C R Mueller 1, M Begbie 1, C R Notley 1, D Lillicrap 1
PMCID: PMC231181  PMID: 8628260

Abstract

Coagulation factor VIII is an essential cofactor required for normal hemostatic function. A deficiency in factor VIII results in the bleeding disorder hemophilia A. Despite the fact that the factor VIII gene was cloned a decade ago, the mechanisms which control its transcription remain unresolved. In our studies, we have characterized 12 protein binding sites within the factor VIII promoter by DNase I protection assays performed with rat liver nuclear extracts. Three of these elements (sites 1 to 3) are situated within the 5' untranslated region of the gene, while three other sites (sites 4 to 6) lie within the first 100 bp upstream of the transcriptional start site. We have identified an additional site (site 7) approximately 300 bp upstream from site 6, as well as a cluster of five sites in a 250-bp region which terminates approximately 1 kb from the transcriptional start site. Seven of these binding sites (sites 2, 3, 4, 6, 7, 9, and 10) bind members of the C/EBP family of transcription factors. DBP also binds to five of these sites (sites 3, 4, 6, 7, and 9). Utilizing transient transfection studies in HepG2 cells, we have shown that deletion of the factor VIII promoter sequences distal to nucleotide -44 results in a significant but small increase in promoter activity. The activity of each of the various 5' deletion constructs is significantly enhanced by cotransfection of C/EBPalpha and D-site-binding protein expression plasmids, while cotransfection of both C/EBPalpha and C/EBPbeta plasmids resulted in a further enhancement of transactivation. These studies also provide evidence of a repressor element located between nucleotides -740 and -1002. Since the minimal promoter sequence (-44 to +148) maintains the transcriptional activity of the full-length promoter sequence, we proceeded to identify additional factors binding to sites 1 to 4. Competition studies revealed that a ubiquitous transcription factor, NF-Y, binds to site 4, while the liver-enriched transcription factor hepatocyte nuclear factor I (HNF-1) binds to site 1. Mutation analysis of the minimal promoter demonstrated that HNF-1 is critical for activating transcription of the factor VIII gene in vitro. Our results also suggest that the multiple upstream elements that we have identified may act as a backup regulatory region in the event of disruption of the HNF-1 element in the 5' untranslated region.

Full Text

The Full Text of this article is available as a PDF (479.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bach I., Mattei M. G., Cereghini S., Yaniv M. Two members of an HNF1 homeoprotein family are expressed in human liver. Nucleic Acids Res. 1991 Jul 11;19(13):3553–3559. doi: 10.1093/nar/19.13.3553. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bontempo F. A., Lewis J. H., Gorenc T. J., Spero J. A., Ragni M. V., Scott J. P., Starzl T. E. Liver transplantation in hemophilia A. Blood. 1987 Jun;69(6):1721–1724. [PMC free article] [PubMed] [Google Scholar]
  3. Briët E., Bertina R. M., van Tilburg N. H., Veltkamp J. J. Hemophilia B Leyden: a sex-linked hereditary disorder that improves after puberty. N Engl J Med. 1982 Apr 1;306(13):788–790. doi: 10.1056/NEJM198204013061306. [DOI] [PubMed] [Google Scholar]
  4. Courtois G., Baumhueter S., Crabtree G. R. Purified hepatocyte nuclear factor 1 interacts with a family of hepatocyte-specific promoters. Proc Natl Acad Sci U S A. 1988 Nov;85(21):7937–7941. doi: 10.1073/pnas.85.21.7937. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Crossley M., Brownlee G. G. Disruption of a C/EBP binding site in the factor IX promoter is associated with haemophilia B. Nature. 1990 May 31;345(6274):444–446. doi: 10.1038/345444a0. [DOI] [PubMed] [Google Scholar]
  6. Crossley M., Winship P. R., Austen D. E., Rizza C. R., Brownlee G. G. A less severe form of Haemophilia B Leyden. Nucleic Acids Res. 1990 Aug 11;18(15):4633–4633. doi: 10.1093/nar/18.15.4633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dorner A. J., Bole D. G., Kaufman R. J. The relationship of N-linked glycosylation and heavy chain-binding protein association with the secretion of glycoproteins. J Cell Biol. 1987 Dec;105(6 Pt 1):2665–2674. doi: 10.1083/jcb.105.6.2665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dorner A. J., Wasley L. C., Kaufman R. J. Protein dissociation from GRP78 and secretion are blocked by depletion of cellular ATP levels. Proc Natl Acad Sci U S A. 1990 Oct;87(19):7429–7432. doi: 10.1073/pnas.87.19.7429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Elion J., Berg P. E., Lapouméroulie C., Trabuchet G., Mittelman M., Krishnamoorthy R., Schechter A. N., Labie D. DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation. Blood. 1992 Feb 1;79(3):787–792. [PubMed] [Google Scholar]
  10. Figueiredo M. S., Brownlee G. G. cis-acting elements and transcription factors involved in the promoter activity of the human factor VIII gene. J Biol Chem. 1995 May 19;270(20):11828–11838. doi: 10.1074/jbc.270.20.11828. [DOI] [PubMed] [Google Scholar]
  11. Friedman A. D., Landschulz W. H., McKnight S. L. CCAAT/enhancer binding protein activates the promoter of the serum albumin gene in cultured hepatoma cells. Genes Dev. 1989 Sep;3(9):1314–1322. doi: 10.1101/gad.3.9.1314. [DOI] [PubMed] [Google Scholar]
  12. Gitschier J., Wood W. I., Goralka T. M., Wion K. L., Chen E. Y., Eaton D. H., Vehar G. A., Capon D. J., Lawn R. M. Characterization of the human factor VIII gene. Nature. 1984 Nov 22;312(5992):326–330. doi: 10.1038/312326a0. [DOI] [PubMed] [Google Scholar]
  13. Gorski K., Carneiro M., Schibler U. Tissue-specific in vitro transcription from the mouse albumin promoter. Cell. 1986 Dec 5;47(5):767–776. doi: 10.1016/0092-8674(86)90519-2. [DOI] [PubMed] [Google Scholar]
  14. Grant D. J., Maeda N. A base substitution in the promoter associated with the human haptoglobin 2-1 modified phenotype decreases transcriptional activity and responsiveness to interleukin-6 in human hepatoma cells. Am J Hum Genet. 1993 May;52(5):974–980. [PMC free article] [PubMed] [Google Scholar]
  15. Gregori C., Kahn A., Pichard A. L. Competition between transcription factors HNF1 and HNF3, and alternative cell-specific activation by DBP and C/EBP contribute to the regulation of the liver-specific aldolase B promoter. Nucleic Acids Res. 1993 Feb 25;21(4):897–903. doi: 10.1093/nar/21.4.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Higuchi M., Wong C., Kochhan L., Olek K., Aronis S., Kasper C. K., Kazazian H. H., Jr, Antonarakis S. E. Characterization of mutations in the factor VIII gene by direct sequencing of amplified genomic DNA. Genomics. 1990 Jan;6(1):65–71. doi: 10.1016/0888-7543(90)90448-4. [DOI] [PubMed] [Google Scholar]
  17. Hirosawa S., Fahner J. B., Salier J. P., Wu C. T., Lovrien E. W., Kurachi K. Structural and functional basis of the developmental regulation of human coagulation factor IX gene: factor IX Leyden. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4421–4425. doi: 10.1073/pnas.87.12.4421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hoyer L. W. The factor VIII complex: structure and function. Blood. 1981 Jul;58(1):1–13. [PubMed] [Google Scholar]
  19. Kaufman R. J., Wasley L. C., Davies M. V., Wise R. J., Israel D. I., Dorner A. J. Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells. Mol Cell Biol. 1989 Mar;9(3):1233–1242. doi: 10.1128/mcb.9.3.1233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kaufman R. J., Wasley L. C., Dorner A. J. Synthesis, processing, and secretion of recombinant human factor VIII expressed in mammalian cells. J Biol Chem. 1988 May 5;263(13):6352–6362. [PubMed] [Google Scholar]
  21. Lee Y. H., Alberta J. A., Gonzalez F. J., Waxman D. J. Multiple, functional DBP sites on the promoter of the cholesterol 7 alpha-hydroxylase P450 gene, CYP7. Proposed role in diurnal regulation of liver gene expression. J Biol Chem. 1994 May 20;269(20):14681–14689. [PubMed] [Google Scholar]
  22. Lewis J. H., Bontempo F. A., Spero J. A., Ragni M. V., Starzl T. E. Liver transplantation in a hemophiliac. N Engl J Med. 1985 May 2;312(18):1189–1190. doi: 10.1056/NEJM198505023121812. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Lichtsteiner S., Wuarin J., Schibler U. The interplay of DNA-binding proteins on the promoter of the mouse albumin gene. Cell. 1987 Dec 24;51(6):963–973. doi: 10.1016/0092-8674(87)90583-6. [DOI] [PubMed] [Google Scholar]
  24. Ljung R., Nilsson I. M. Hemophilia B Leyden and a similar variant of hemophilia A. N Engl J Med. 1982 Sep 30;307(14):897–898. doi: 10.1056/nejm198209303071422. [DOI] [PubMed] [Google Scholar]
  25. Ludwig M., Schwaab R., Eigel A., Horst J., Egli H., Brackmann H. H., Olek K. Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B. Am J Hum Genet. 1989 Jul;45(1):115–122. [PMC free article] [PubMed] [Google Scholar]
  26. Maire P., Wuarin J., Schibler U. The role of cis-acting promoter elements in tissue-specific albumin gene expression. Science. 1989 Apr 21;244(4902):343–346. doi: 10.1126/science.2711183. [DOI] [PubMed] [Google Scholar]
  27. Meloni A., Rosatelli M. C., Faà V., Sardu R., Saba L., Murru S., Sciarratta G. V., Baldi M., Tannoia N., Vitucci A. Promoter mutations producing mild beta-thalassaemia in the Italian population. Br J Haematol. 1992 Feb;80(2):222–226. doi: 10.1111/j.1365-2141.1992.tb08904.x. [DOI] [PubMed] [Google Scholar]
  28. Mendel D. B., Hansen L. P., Graves M. K., Conley P. B., Crabtree G. R. HNF-1 alpha and HNF-1 beta (vHNF-1) share dimerization and homeo domains, but not activation domains, and form heterodimers in vitro. Genes Dev. 1991 Jun;5(6):1042–1056. doi: 10.1101/gad.5.6.1042. [DOI] [PubMed] [Google Scholar]
  29. Minty A., Kedes L. Upstream regions of the human cardiac actin gene that modulate its transcription in muscle cells: presence of an evolutionarily conserved repeated motif. Mol Cell Biol. 1986 Jun;6(6):2125–2136. doi: 10.1128/mcb.6.6.2125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Mueller C. R. The down-regulation of albumin transcription during regeneration is due to the loss of HNF-1 and the D-site transcription factors. DNA Cell Biol. 1992 Sep;11(7):559–566. doi: 10.1089/dna.1992.11.559. [DOI] [PubMed] [Google Scholar]
  31. Murru S., Pischedda M. C., Cao A., Rosatelli M. C., Pirastu M., Sciarratta G. V., Manca L., Gallisai D., Toffoli C. A promoter mutation of the beta-globin gene (-101 C-->T) has an age-related expression pattern. Blood. 1993 May 15;81(10):2818–2819. [PubMed] [Google Scholar]
  32. Orkin S. H., Antonarakis S. E., Kazazian H. H., Jr Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC. J Biol Chem. 1984 Jul 25;259(14):8679–8681. [PubMed] [Google Scholar]
  33. Orkin S. H., Sexton J. P., Cheng T. C., Goff S. C., Giardina P. J., Lee J. I., Kazazian H. H., Jr ATA box transcription mutation in beta-thalassemia. Nucleic Acids Res. 1983 Jul 25;11(14):4727–4734. doi: 10.1093/nar/11.14.4727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Picketts D. J., D'Souza C., Bridge P. J., Lillicrap D. An A to T transversion at position -5 of the factor IX promoter results in hemophilia B. Genomics. 1992 Jan;12(1):161–163. doi: 10.1016/0888-7543(92)90421-n. [DOI] [PubMed] [Google Scholar]
  35. Picketts D. J., Lillicrap D. P., Mueller C. R. Synergy between transcription factors DBP and C/EBP compensates for a haemophilia B Leyden factor IX mutation. Nat Genet. 1993 Feb;3(2):175–179. doi: 10.1038/ng0293-175. [DOI] [PubMed] [Google Scholar]
  36. Picketts D. J., Mueller C. R., Lillicrap D. Transcriptional control of the factor IX gene: analysis of five cis-acting elements and the deleterious effects of naturally occurring hemophilia B Leyden mutations. Blood. 1994 Nov 1;84(9):2992–3000. [PubMed] [Google Scholar]
  37. Pittman D. D., Kaufman R. J. Structure-function relationships of factor VIII elucidated through recombinant DNA technology. Thromb Haemost. 1989 Apr 25;61(2):161–165. [PubMed] [Google Scholar]
  38. Ratnoff O. D., Lewis J. H. Heckathorn's disease: variable functional dificiency of antihemophilic factor (factor VIII). Blood. 1975 Aug;46(2):161–173. [PubMed] [Google Scholar]
  39. Ray A., Hannink M., Ray B. K. Concerted participation of NF-kappa B and C/EBP heteromer in lipopolysaccharide induction of serum amyloid A gene expression in liver. J Biol Chem. 1995 Mar 31;270(13):7365–7374. doi: 10.1074/jbc.270.13.7365. [DOI] [PubMed] [Google Scholar]
  40. Reijnen M. J., Peerlinck K., Maasdam D., Bertina R. M., Reitsma P. H. Hemophilia B Leyden: substitution of thymine for guanine at position -21 results in a disruption of a hepatocyte nuclear factor 4 binding site in the factor IX promoter. Blood. 1993 Jul 1;82(1):151–158. [PubMed] [Google Scholar]
  41. Reijnen M. J., Sladek F. M., Bertina R. M., Reitsma P. H. Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden. Proc Natl Acad Sci U S A. 1992 Jul 15;89(14):6300–6303. doi: 10.1073/pnas.89.14.6300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Reitsma P. H., Bertina R. M., Ploos van Amstel J. K., Riemens A., Briët E. The putative factor IX gene promoter in hemophilia B Leyden. Blood. 1988 Sep;72(3):1074–1076. [PubMed] [Google Scholar]
  43. Roeder R. G. The complexities of eukaryotic transcription initiation: regulation of preinitiation complex assembly. Trends Biochem Sci. 1991 Nov;16(11):402–408. doi: 10.1016/0968-0004(91)90164-q. [DOI] [PubMed] [Google Scholar]
  44. Royle G., Van de Water N. S., Berry E., Ockelford P. A., Browett P. J. Haemophilia B Leyden arising de novo by point mutation in the putative factor IX promoter region. Br J Haematol. 1991 Feb;77(2):191–194. doi: 10.1111/j.1365-2141.1991.tb07976.x. [DOI] [PubMed] [Google Scholar]
  45. Smale S. T., Baltimore D. The "initiator" as a transcription control element. Cell. 1989 Apr 7;57(1):103–113. doi: 10.1016/0092-8674(89)90176-1. [DOI] [PubMed] [Google Scholar]
  46. Stein B., Baldwin A. S., Jr Distinct mechanisms for regulation of the interleukin-8 gene involve synergism and cooperativity between C/EBP and NF-kappa B. Mol Cell Biol. 1993 Nov;13(11):7191–7198. doi: 10.1128/mcb.13.11.7191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Svensson E. C., Conley P. B., Paulson J. C. Regulated expression of alpha 2,6-sialyltransferase by the liver-enriched transcription factors HNF-1, DBP, and LAP. J Biol Chem. 1992 Feb 15;267(5):3466–3472. [PubMed] [Google Scholar]
  48. Toole J. J., Knopf J. L., Wozney J. M., Sultzman L. A., Buecker J. L., Pittman D. D., Kaufman R. J., Brown E., Shoemaker C., Orr E. C. Molecular cloning of a cDNA encoding human antihaemophilic factor. Nature. 1984 Nov 22;312(5992):342–347. doi: 10.1038/312342a0. [DOI] [PubMed] [Google Scholar]
  49. Tuddenham E. G., Schwaab R., Seehafer J., Millar D. S., Gitschier J., Higuchi M., Bidichandani S., Connor J. M., Hoyer L. W., Yoshioka A. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Res. 1994 Nov 11;22(22):4851–4868. doi: 10.1093/nar/22.22.4851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Vehar G. A., Keyt B., Eaton D., Rodriguez H., O'Brien D. P., Rotblat F., Oppermann H., Keck R., Wood W. I., Harkins R. N. Structure of human factor VIII. Nature. 1984 Nov 22;312(5992):337–342. doi: 10.1038/312337a0. [DOI] [PubMed] [Google Scholar]
  51. Vuorio T., Maity S. N., de Crombrugghe B. Purification and molecular cloning of the "A" chain of a rat heteromeric CCAAT-binding protein. Sequence identity with the yeast HAP3 transcription factor. J Biol Chem. 1990 Dec 25;265(36):22480–22486. [PubMed] [Google Scholar]
  52. Wieland K., Berg L. P., Kakkar V. V., Cooper D. N., Martinowitz U. Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIII. Thromb Res. 1990 Sep 1;59(5):871–877. doi: 10.1016/0049-3848(90)90400-7. [DOI] [PubMed] [Google Scholar]
  53. Wion K. L., Kelly D., Summerfield J. A., Tuddenham E. G., Lawn R. M. Distribution of factor VIII mRNA and antigen in human liver and other tissues. Nature. 1985 Oct 24;317(6039):726–729. doi: 10.1038/317726a0. [DOI] [PubMed] [Google Scholar]
  54. Wood W. I., Capon D. J., Simonsen C. C., Eaton D. L., Gitschier J., Keyt B., Seeburg P. H., Smith D. H., Hollingshead P., Wion K. L. Expression of active human factor VIII from recombinant DNA clones. Nature. 1984 Nov 22;312(5992):330–337. doi: 10.1038/312330a0. [DOI] [PubMed] [Google Scholar]
  55. Wuarin J., Mueller C., Schibler U. A ubiquitous CCAAT factor is required for efficient in vitro transcription from the mouse albumin promoter. J Mol Biol. 1990 Aug 20;214(4):865–874. doi: 10.1016/0022-2836(90)90341-I. [DOI] [PubMed] [Google Scholar]

Articles from Molecular and Cellular Biology are provided here courtesy of Taylor & Francis

RESOURCES