Skip to main content
Molecular and Cellular Biology logoLink to Molecular and Cellular Biology
. 1995 Mar;15(3):1439–1445. doi: 10.1128/mcb.15.3.1439

Basal promoter of the rat connexin 32 gene: identification and characterization of an essential element and its DNA-binding protein.

S Bai 1, A Schoenfeld 1, A Pietrangelo 1, R D Burk 1
PMCID: PMC230368  PMID: 7862137

Abstract

The connexin 32 (Cx32) gene, a member of a multigene family, is expressed preferentially in the liver. The basal promoter complex of the rat Cx32 gene was previously localized to a 146-bp region (map positions [mp] -179 to -34) immediately upstream of the first exon. To investigate the biochemical factors contributing to the basal promoter activity, nuclear protein-DNA complexes within this region (mp -177 to -106) were investigated by using a DNA mobility shift assay. Three DNA-protein binding activities, termed Cx32-B1, Cx32-B2, and Cx32-B3, were identified with nuclear protein extracts from hepatoma cell lines, HuH7 and FAO-1. However, only Cx32-B2 binding activity was detected in nuclear protein extract from normal rat liver tissue. This activity was significantly more abundant in rat liver tissue than in hepatoma cell lines and tissues from various other organs. By using methylation interference footprinting, the Cx32-B2 complex was localized to the region between mp -152 and -127 and a DNA probe containing this region bound to a 60-kDa protein in rat liver nuclear extracts. Mutation of two nucleotides in the Cx32-B2 binding site abrogated the formation of the Cx32-B2 protein-DNA complex and significantly reduced the transcriptional activity of the Cx32 promoter. These results indicate that the Cx32-B2 complex is an essential component of the rat Cx32 basal promoter and is likely a major factor in the preferential expression of this gene in the liver.

Full Text

The Full Text of this article is available as a PDF (438.7 KB).

Selected References

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

  1. Ammendola R., Mesuraca M., Russo T., Cimino F. Sp1 DNA binding efficiency is highly reduced in nuclear extracts from aged rat tissues. J Biol Chem. 1992 Sep 5;267(25):17944–17948. [PubMed] [Google Scholar]
  2. Bai S., Spray D. C., Burk R. D. Identification of proximal and distal regulatory elements of the rat connexin32 gene. Biochim Biophys Acta. 1993 Nov 16;1216(2):197–204. doi: 10.1016/0167-4781(93)90145-4. [DOI] [PubMed] [Google Scholar]
  3. Beer D. G., Neveu M. J., Paul D. L., Rapp U. R., Pitot H. C. Expression of the c-raf protooncogene, gamma-glutamyltranspeptidase, and gap junction protein in rat liver neoplasms. Cancer Res. 1988 Mar 15;48(6):1610–1617. [PubMed] [Google Scholar]
  4. Bergoffen J., Scherer S. S., Wang S., Scott M. O., Bone L. J., Paul D. L., Chen K., Lensch M. W., Chance P. F., Fischbeck K. H. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 1993 Dec 24;262(5142):2039–2042. doi: 10.1126/science.8266101. [DOI] [PubMed] [Google Scholar]
  5. Brasier A. R., Tate J. E., Habener J. F. Optimized use of the firefly luciferase assay as a reporter gene in mammalian cell lines. Biotechniques. 1989 Nov-Dec;7(10):1116–1122. [PubMed] [Google Scholar]
  6. Buratowski S. The basics of basal transcription by RNA polymerase II. Cell. 1994 Apr 8;77(1):1–3. doi: 10.1016/0092-8674(94)90226-7. [DOI] [PubMed] [Google Scholar]
  7. De Simone V., Cortese R. Transcription factors and liver-specific genes. Biochim Biophys Acta. 1992 Sep 24;1132(2):119–126. doi: 10.1016/0167-4781(92)90001-g. [DOI] [PubMed] [Google Scholar]
  8. Dermietzel R., Hwang T. K., Spray D. S. The gap junction family: structure, function and chemistry. Anat Embryol (Berl) 1990;182(6):517–528. doi: 10.1007/BF00186458. [DOI] [PubMed] [Google Scholar]
  9. Dermietzel R., Spray D. C. Gap junctions in the brain: where, what type, how many and why? Trends Neurosci. 1993 May;16(5):186–192. doi: 10.1016/0166-2236(93)90151-b. [DOI] [PubMed] [Google Scholar]
  10. Dermietzel R., Traub O., Hwang T. K., Beyer E., Bennett M. V., Spray D. C., Willecke K. Differential expression of three gap junction proteins in developing and mature brain tissues. Proc Natl Acad Sci U S A. 1989 Dec;86(24):10148–10152. doi: 10.1073/pnas.86.24.10148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Deryckere F., Gannon F. A one-hour minipreparation technique for extraction of DNA-binding proteins from animal tissues. Biotechniques. 1994 Mar;16(3):405–405. [PubMed] [Google Scholar]
  12. Dignam J. D., Lebovitz R. M., Roeder R. G. Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei. Nucleic Acids Res. 1983 Mar 11;11(5):1475–1489. doi: 10.1093/nar/11.5.1475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fishman G. I., Eddy R. L., Shows T. B., Rosenthal L., Leinwand L. A. The human connexin gene family of gap junction proteins: distinct chromosomal locations but similar structures. Genomics. 1991 May;10(1):250–256. doi: 10.1016/0888-7543(91)90507-b. [DOI] [PubMed] [Google Scholar]
  14. Fitzgerald D. J., Mesnil M., Oyamada M., Tsuda H., Ito N., Yamasaki H. Changes in gap junction protein (connexin 32) gene expression during rat liver carcinogenesis. J Cell Biochem. 1989 Oct;41(2):97–102. doi: 10.1002/jcb.240410206. [DOI] [PubMed] [Google Scholar]
  15. Gimlich R. L., Kumar N. M., Gilula N. B. Differential regulation of the levels of three gap junction mRNAs in Xenopus embryos. J Cell Biol. 1990 Mar;110(3):597–605. doi: 10.1083/jcb.110.3.597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hattori M., Tugores A., Veloz L., Karin M., Brenner D. A. A simplified method for the preparation of transcriptionally active liver nuclear extracts. DNA Cell Biol. 1990 Dec;9(10):777–781. doi: 10.1089/dna.1990.9.777. [DOI] [PubMed] [Google Scholar]
  17. Hoey T., Weinzierl R. O., Gill G., Chen J. L., Dynlacht B. D., Tjian R. Molecular cloning and functional analysis of Drosophila TAF110 reveal properties expected of coactivators. Cell. 1993 Jan 29;72(2):247–260. doi: 10.1016/0092-8674(93)90664-c. [DOI] [PubMed] [Google Scholar]
  18. Kren B. T., Kumar N. M., Wang S. Q., Gilula N. B., Steer C. J. Differential regulation of multiple gap junction transcripts and proteins during rat liver regeneration. J Cell Biol. 1993 Nov;123(3):707–718. doi: 10.1083/jcb.123.3.707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  20. 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]
  21. Maxam A. M., Gilbert W. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 1980;65(1):499–560. doi: 10.1016/s0076-6879(80)65059-9. [DOI] [PubMed] [Google Scholar]
  22. Miller T., Dahl G., Werner R. Structure of a gap junction gene: rat connexin-32. Biosci Rep. 1988 Oct;8(5):455–464. doi: 10.1007/BF01121644. [DOI] [PubMed] [Google Scholar]
  23. Neveu M. J., Hully J. R., Babcock K. L., Hertzberg E. L., Nicholson B. J., Paul D. L., Pitot H. C. Multiple mechanisms are responsible for altered expression of gap junction genes during oncogenesis in rat liver. J Cell Sci. 1994 Jan;107(Pt 1):83–95. doi: 10.1242/jcs.107.1.83. [DOI] [PubMed] [Google Scholar]
  24. Neveu M. J., Hully J. R., Paul D. L., Pitot H. C. Reversible alteration in the expression of the gap junctional protein connexin 32 during tumor promotion in rat liver and its role during cell proliferation. Cancer Commun. 1990;2(1):21–31. doi: 10.3727/095535490820874731. [DOI] [PubMed] [Google Scholar]
  25. Paul D. L. Molecular cloning of cDNA for rat liver gap junction protein. J Cell Biol. 1986 Jul;103(1):123–134. doi: 10.1083/jcb.103.1.123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Pugh B. F., Tjian R. Mechanism of transcriptional activation by Sp1: evidence for coactivators. Cell. 1990 Jun 29;61(7):1187–1197. doi: 10.1016/0092-8674(90)90683-6. [DOI] [PubMed] [Google Scholar]
  27. Rosenberg E., Spray D. C., Reid L. M. Transcriptional and posttranscriptional control of connexin mRNAs in periportal and pericentral rat hepatocytes. Eur J Cell Biol. 1992 Oct;59(1):21–26. [PubMed] [Google Scholar]
  28. Sakamoto H., Oyamada M., Enomoto K., Mori M. Differential changes in expression of gap junction proteins connexin 26 and 32 during hepatocarcinogenesis in rats. Jpn J Cancer Res. 1992 Nov;83(11):1210–1215. doi: 10.1111/j.1349-7006.1992.tb02747.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Spray D. C., Chanson M., Moreno A. P., Dermietzel R., Meda P. Distinctive gap junction channel types connect WB cells, a clonal cell line derived from rat liver. Am J Physiol. 1991 Mar;260(3 Pt 1):C513–C527. doi: 10.1152/ajpcell.1991.260.3.C513. [DOI] [PubMed] [Google Scholar]
  30. Spray D. C., Fujita M., Saez J. C., Choi H., Watanabe T., Hertzberg E., Rosenberg L. C., Reid L. M. Proteoglycans and glycosaminoglycans induce gap junction synthesis and function in primary liver cultures. J Cell Biol. 1987 Jul;105(1):541–551. doi: 10.1083/jcb.105.1.541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Tjian R., Maniatis T. Transcriptional activation: a complex puzzle with few easy pieces. Cell. 1994 Apr 8;77(1):5–8. doi: 10.1016/0092-8674(94)90227-5. [DOI] [PubMed] [Google Scholar]
  32. Traub O., Look J., Paul D., Willecke K. Cyclic adenosine monophosphate stimulates biosynthesis and phosphorylation of the 26 kDa gap junction protein in cultured mouse hepatocytes. Eur J Cell Biol. 1987 Feb;43(1):48–54. [PubMed] [Google Scholar]
  33. Weis L., Reinberg D. Transcription by RNA polymerase II: initiator-directed formation of transcription-competent complexes. FASEB J. 1992 Nov;6(14):3300–3309. doi: 10.1096/fasebj.6.14.1426767. [DOI] [PubMed] [Google Scholar]
  34. Zhang J. T., Nicholson B. J. Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA. J Cell Biol. 1989 Dec;109(6 Pt 2):3391–3401. doi: 10.1083/jcb.109.6.3391. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES