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Trans-acting factors that interact with the proximal promoter sequences of ovalbumin gene are tissue-specific and age-related

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Abstract

Aging or deterioration of functions of various organs occurs after adulthood due to alterations in the expression of genes that maintain adulthood functions. Molecular changes that occur in regulation of genes in higher organisms after adulthood can be understood by using genes whose timing and rate of expression run parallel with specific functions during the life span. One such function is egg formation in birds which is dependent on the expression of egg protein genes, ovalbumin, lysozyme, vitellogenin, etc. Trans-acting factors are known to play a pivotal role in the regulation of transcription of genes. We show here a decrease in the level/binding of nuclear trans-acting factors with specific cis-acting elements of the promoter of the ovalbumin gene of oviduct of old Japanese quail. This parallels the decrease in the expression of the ovalbumin gene in the oviduct after adulthood. These factors are tissue-specific and bind in a cooperative and sequential manner to the ovalbumin gene promoter.

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References

  1. Mitchell PJ, Tjian R: Transcriptional regulation in mammalian cells by sequence specific DNA binding proteins. Science 245: 371–378, 1989

    Google Scholar 

  2. Tjian R, Maniatis T: Transcriptional activation: A complex puzzle with few easy pieces. Cell 77: 5–8, 1994

    Google Scholar 

  3. Woo SLC, Beattie WG, Catterall JF, Dugaiczyk A, Staden R, Brownlee GG, O'Malley BW: Complete nucleotide sequence of the chicken chromosomal ovalbumin gene and its biological significance. Biochemistry 20: 6437–6446, 1981.

    Google Scholar 

  4. Kaye JS, Pratt-Kaye S, Bellard M, Dretzen G, Bellard F, Chambon P: Steroid hormone dependence of four DNaseI-hypersensitive regions located within the 7000 bp 5′-flanking segment of the ovalbumin gene. EMBO J 5: 277–285, 1986

    Google Scholar 

  5. Bellard M, Dretzen G, Bellard F, Kay JS, Pratt-Kaye S, Chambon P: Disruption of the total chromatin structure in a 2500 bp region at the 5′ end of the actively transcribed ovalbumin gene. EMBO J 5: 567–574, 1986

    Google Scholar 

  6. Upadhyay R, Gupta S, Kanungo MS: Age-related changes in the ovalbumin gene of the Japanese quail. Biochem Biophys Res Commun 226: 256–261, 1996

    Google Scholar 

  7. Gaub M-P, Dierich A, Astinotti I, Touitou I, Chambon P: The chicken ovalbumin promoter is under negative control which is relieved by steroid hormones. EMBO J 6: 2313–2320, 1987.

    Google Scholar 

  8. Pastoric M, Bagchi MK, Tsai SY, Tsai MJ, O'Malley BW: Multiple protein binding sites within the 5′-flanking region: Isolation and characterization of sequence-specific binding proteins. Nucl Acid Res 17: 6693–6711, 1989

    Google Scholar 

  9. Heilig R, Muraskowsky R, Mandel JL: The ovalbumin gene family: The 5′ region of X and Y genes. J Mol Biol 156: 4363–4382, 1982.

    Google Scholar 

  10. Nordstrom LA, Dean DM, Sanders MM: A complex array of doublestranded and single-stranded DNA-binding proteins mediate induction of the ovalbumin gene by steroid hormones. J Biol Chem 268: 13193–13202, 1993.

    Google Scholar 

  11. Sanders MM, McKnight GS: Egg white genes: Hormonal regulation in homologous and heterologous cells. In: G.M. Mlacinski (ed). Molecular Genetics of Mammlian Cells. 1986, pp 183–216.

  12. Dierich A, Gaub MP, LePennec JP, Astinotti D, Chambon P: Cell specificity of the chicken ovalbumin and conalbumin promoter. EMBO J 6: 2305–2312, 1987

    Google Scholar 

  13. Tora L, Gaub MP, Mader S, Dierich A, Bellard M, Chambon P: Cellspecific activity of a GGTCA half palindrome estrogen-responsive element in the chicken ovalbumin gene promoter. EMBO J 7: 3771–3778, 1988

    Google Scholar 

  14. Wang LH, Tsai SY, Cook RG, Beattie WG, Tsai MJ, O'Malley BW: COUP-TF is a member of the steroid receptor superfamily. Nature 340: 163–166, 1989

    Google Scholar 

  15. Sambrook J, Fritsh EF, Maniatis T: Molecular cloning: A Laboratory Manual. Cold Spring Harbour Laboratory Press, 1989

  16. Kuhl D, Fuente J de la, Chaturvedi M, Parimoo S, Ryals J, Meyer F, Weissmann C: Reversible silencing of enhancers by sequences derived from the human IFN-Alpha promoter. Cell 50: 1057–1069, 1987

    Google Scholar 

  17. Gorski K, Carneiro M, Schibler U: Tissue-specific in vitro transcription from the mouse albumin promoter. Cell 47: 667–676, 1986

    Google Scholar 

  18. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ: Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265–275, 1951

    Google Scholar 

  19. Fukuda H, Iritani N: Effects of aging on gene expression of acetyl-CoA carboxylase and fatty acid synthase in rat liver. J Biochem 112: 277–280, 1992

    Google Scholar 

  20. Heydari AR, Wu B, Takahashi R, Strong R, Richardson A: Expression of heat shock protein 70 is altered by age and diet at the level of transcription. Mol Cell Biol 13: 2909–2918, 1993

    Google Scholar 

  21. Kanungo MS: Genes and aging. Cambridge University Press, New York, 1994

    Google Scholar 

  22. Chaturvedi MM, Kanungo MS: Analysis of chromatin of the brain of young and old rats by micrococcal nuclease and DNaseI. Biochem Int 6: 1357–1363, 1983

    Google Scholar 

  23. Singh S, Kanungo MS: Changes in expression and CRE binding proteins of the fibronectin gene of the liver of the rat. Biochem Biophys Res Commun 193: 440–445, 1993

    Google Scholar 

  24. Gupta S, Upadhyay R, Kanungo MS: Activation of vitellogenin II gene expression by steroid hormones in old Japanese quail. Molec Biol Rep 25: 245–251, 1998

    Google Scholar 

  25. Kornberg RD, Lorch Y: Irresistible force meets immovable objects: Transcription and the nucleosomes. Cell 67: 833–836, 1991

    Google Scholar 

  26. Roeder RG: Role of general initiation factors in transcription by RNA polymerase II. Trends in Biochem. 21: 327–335, 1996

    Google Scholar 

  27. Birkenmeier EH, Gwynn B, Howard S, Jerry J, Gordon JI, Landschulz WH, McKnight SL: Tissue-specific expression, developmental regulation and genetic mapping of the gene encoding CCAAT/enhancer binding protein. Genes & Dev 3: 1146–1156, 1989

    Google Scholar 

  28. Gaub MP, Bellard M, Scheuer I, Chambon P: Activation of the ovalbumin gene by estrogen receptor involves Fos-Jun complex. Cell 63: 1267–1276, 1990

    Google Scholar 

  29. Riabowol K, Schiff J, Gilman MZ: Transcription factor AP-1 activity is required for initiation of DNA synthesis and is lost during cellular aging. Proc Natl Acad Sci USA 89: 157–161, 1992

    Google Scholar 

  30. Sikora E, Kaminska B, Radziszewska E, Kaczmarek L: Loss of transcription factor AP-1 DNA binding activity during lymphocyte aging in vivo. FEBS Lett 312: 179–182, 1992

    Google Scholar 

  31. Ron D, Habener JF: Genes & Dev 6: 439–453, 1992

    Google Scholar 

  32. Cooney AJ, Tsai SY, O'Malley BW, Tsai MJ: COUP-TF dimers bind to different GGTCA response elements, allowing it to repress hormonal induction of the vit D3, thyroid hormone and retinoic acid receptor. Mol Cell Biol 12: 4153–4163, 1992

    Google Scholar 

  33. Burbach JPH, da Silva SL, Cox JJ, Adan RAH, Cooney AJ, Tsai M-J, Tsai SY: Repression of estrogen-dependent stimulation of oxytocin gene by COUP-TF 1. J Biol Chem 269: 15046–15053, 1994

    Google Scholar 

  34. Liu Y, Yang N, Teng C: COUP-TF acts as a competitive repressor of estrogen receptor mediated activation of mouse lactoferrins gene. Mol Cell Biol 13: 1836–1846, 1993

    Google Scholar 

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Upadhyay, R., Gupta, S. & Kanungo, M. Trans-acting factors that interact with the proximal promoter sequences of ovalbumin gene are tissue-specific and age-related. Mol Cell Biochem 201, 65–72 (1999). https://doi.org/10.1023/A:1007000215524

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  • DOI: https://doi.org/10.1023/A:1007000215524

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