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Analysis of an alternative promoter that regulates tissue-specific expression of the human aromatic L-amino acid decarboxylase gene in cultured cell lines

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Summary

The human aromatic L-amino acid decarboxylase (AADC) gene is transcribed in a tissue-specific manner by an alternative promoter. In this study using human cultured cell lines, we analyzed the alternative promoter that regulates tissue-specific expression of AADC. Neither neuronalnor nonneuronal-type mRNA of AADC was detected in HeLa cells, nonneuronal-type mRNA of AADC was expressed in HepG2 cells, and the neuronal-type was expressed in the SK-N-SH cell line. We examined the promoter activities located in 5′- and 3′-flanking regions of exon N1 and exon L1 by transfection experiments. Plasmids containing 5′-flanking regions of exon L1, the shortest of which was 0.3kb, could promote specifically high expression of the reporter gene in HepG2 cells. On the other hand, plasmids containing 5′-flanking regions of exon N1 (3.6 kb to 0.5 kb) could promote the reporter gene expression not only in SK-N-SH cells but also in HeLa and HepG2. More enhanced expression were observed by transfection of plasmids containing parts of the first intron in these cell lines. Thus, these results suggest that the basal liver-specific promoter activity is located in the 5′-flanking region of exon L1 and that the first intron may also be needed for enhanced expression rather than determination of cell-specificity.

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Abbreviations

AADC :

aromatic L-amino acid decarboxylase

DA :

Dopamine

L-DOPA :

L-3,4,-dihydroxyphenylalanine

L-5-HTP :

L-5-hydroxytryptophan

5-HT :

serotonine

APUD :

amine precursor uptake and decarboxylation

CAT :

chloramphenicolacetyltransferase

RT-PCR :

reverse transcription-PCR

EGTA :

ethylene glycol-bis (β-aminoethyl ether)-N, N, N′, N′-tetraacetic acid

ONPG :

o-nitrophenyl-β-D-galactopyranoside

RLU :

relative light unit

References

  • Albert VR, Lee MR, Bolden AH, Wurzburger RJ, Aguanno A (1992) Distinct promoters direct neuronal and nonneuronal expression of rat aromatic L-amino acid decarboxylase. Proc Natl Acad Sci USA 89: 12053–12057

    Google Scholar 

  • Baylin SB, Abeloff MD, Goodwin G, Carney DM, Gazdar AF (1980) Activity of L-DOPA decarboxylase and diamine oxidase (histamine) in human lung cancers and decarboxylase as a marker for small (oat) cell carcinoma in cell culture. Cancer Res 40: 1990–1994

    Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254

    Google Scholar 

  • Courtois G, Morgan JG, Campbell LA, Fourel G, Crabtree GR (1987) Interaction of a liver-specific nuclear factor with the fibrinogen and α1-antitrypsin promoters. Science 238: 688–692

    Google Scholar 

  • Forss-Petter S, Danielson PE, Catsicas S, Battenberg E, Price J, Nirenberg M, Sutciffe JG (1990) Transgenic mice expressing \-galactosidase in mature neurons under neuronspecific enolase promoter control. Neuron 5: 187–197

    Google Scholar 

  • González-Crespo S, Boronat A (1991) Expression of the rat growth hormone-releasing hormone gene in placenta is directed by an alternative promoter. Proc Natl Acad Sci USA 88: 8749–8753

    Google Scholar 

  • Hahn SL, Hahn M, Kang UJ, Joh TH (1993) Structure of the rat aromatic L-amino acid decarboxylase gene: evidence for an alternative promoter usage. J Neurochem 60: 1058–1064

    Google Scholar 

  • Hayashi M, Yamaji Y, Kitajima W, Saruta T (1990) Aromatic L-amino acid decarboxylase activity along the rat nephron. Am J Physiol 258: F28-F33

    Google Scholar 

  • Ichinose H, Kurosawa Y, Titani K, Fujita K, Nagatsu T (1989) Isolation and characterization of a cDNA clone encoding human aromatic L-amino acid decarboxylase. Biochem Biophys Res Commun 164: 1024–1030

    Google Scholar 

  • Ichinose H, Sumi-Ichinose C, Ohye T, Hagino Y, Fujita K, Nagatsu T (1992) Tissuespecific alternative splicing of the first exon generates two types of mRNAs in human aromatic L-amino acid decarboxylase. Biochemistry 31: 11546–11550

    Google Scholar 

  • Ip YT, Granner DK, Chalkley R (1989) Hormonal regulation of phosphoenolpyruvate carboxykinase gene expression is mediated through modulation of an already disrupted chromatin structure. Mol Cell Biol 9: 1289–1297

    Google Scholar 

  • Ishiguro H, Kim KT, Joh TH, Kim K-S (1993) Neuron-specific expression of the human dopamine β-hydroxylase gene requires both the cAMP-response element and a silencer region. J Biol Chem 268: 17987–17994

    Google Scholar 

  • Jaeger CB, Teitelman G, Joh TH, Albert VR, Park DH, Reis DJ (1983) Some neurons of the rat central nervous system contain aromatic-L-amino-acid decarboxylase but not monoamines. Science 219: 1233–1235

    Google Scholar 

  • Kraner SD, Chong JA, Tsay H-J, Mandel G (1992) Silencing the type II sodium channel gene: a model for neural-specific gene regulation. Neuron 9: 37–44

    Google Scholar 

  • Le Van Thai A, Coste E, Allen JM, Palmiter RD, Weber WJ (1993) Identification of a neuron-specific promoter of human aromatic L-amino acid decarboxylase gene. Mol Brain Res 17: 227–238

    Google Scholar 

  • Li X-M, Juorio AV, Boulton AA (1993) NSD-1015 alters the gene expression of aromatic L-amino acid decarboxylase in rat PC12 pheochromocytoma cells. Neurochem Res 18: 915–919

    Google Scholar 

  • Li X-M, Juorio AV, Boulton AA (1994) Induction of aromatic L-amino acid decarboxylase mRNA by interleukin-1β and prostaglandin E2 in PC12 cells. Neurochem Res 19: 591–595

    Google Scholar 

  • Lovenberg W, Weissbach H, Udenfriend S (1962) Aromatic L-amino acid decarboxylase. J Biol Chem 237: 89–93

    Google Scholar 

  • McKnight SL, Lane MD, Gluecksohn-Waelsch S (1989) Is CCAAT/enhancer-binding protein a central regulator of energy metabolism? Genes Dev 3: 2021–2024

    Google Scholar 

  • Morgan BA, Johnson WA, Hirsh J (1986) Regulated splicing produces different forms of dopa decarboxylase in the central nervous system and hypoderm of Drosophila melanogaster. EMBO J 5: 3335–3342

    Google Scholar 

  • Mori N, Schoenherr C, Vandenbergh DJ, Anderson DJ (1992) A common silencer element in the SCG10 and type II Na+ channel genes binds a factor present in nonneuronal cells but not in neuronal cells. Neuron 9: 45–54

    Google Scholar 

  • Morinaga T, Yasuda H, Hashimoto T, Higashio K, Tamaoki T (1991) A human α-fetoprotein enhancer-binding protein, ATBF1, contains four homeodomains and seventeen zinc fingers. Mol Cell Biol 11: 6041–6049

    Google Scholar 

  • Nagatsu T, Ichinose H, Kojima K, Kameya T, Shimase J, Kodama T, Shimosato Y (1985) Aromatic L-amino acid decarboxylase activities in human lung tissues: comparison between normal lung and lung carcinomas. Biochem Med 34: 52–59

    Google Scholar 

  • Nakajima-Iijima S, Hamada H, Reddy P, Kakunaga T(1985) Molecular structure of the human cytoplasmic β-actin gene: interspecies homology of sequences in the introns. Proc Natl Acad Sci USA 82: 6133–6137

    Google Scholar 

  • Ow DW, Wood KV, DeLuca M, de Wet JR, Helinski DR, Howell SH (1986) Transient and stable expression of the firefly luciferase gene in plant cells and transgenic plants. Science 234: 856–859

    Google Scholar 

  • Paranjape SM, Kamakaka RT, Kadonaga JT (1994) Role of chromatin structure in the regulation of transcription by RNA polymerase II. Annu Rev Biochem 63: 265–297

    Google Scholar 

  • Pearse AGE (1969) The cytochemistry and ultrastructure of polypeptide hormone-producing cells of the APUD series and the embryologic, physiologic and pathologic implications of the concept. J Histochem Cytochem 17: 303–313

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning. A laboratory manual, 2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York

    Google Scholar 

  • Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467

    Google Scholar 

  • Smith CWJ, Patton JG, Nadal-Ginard B (1989) Alternative splicing in the control of gene expression. Annu Rev Genet 23: 527–577

    Google Scholar 

  • Sumi-Ichinose C, Hasegawa S, Ichinose H, Sawada H, Kobayashi K, Sakai M, Fujii T, Nomura H, Nomura T, Nagatsu I, Hagino Y, Fujita K, Nagatsu T (in press) Analysis of the alternative promoters that regulate tissue-specific expression of human aromatic L-amino acid decarboxylase. J Neurochem

  • Sumi-Ichinose C, Ichinose H, Takahashi E, Hori T, Nagatsu T (1992) Molecular cloning of genomic DNA and chromosomal assignment of the gene for human aromatic L-amino acid decarboxylase, the enzyme for catecholamine and serotonin biosynthesis. Biochemistry 31: 2229–2238

    Google Scholar 

  • Vidal M, Morris R, Grosveld F, Spanopoulou E (1990) Tissue-specific control elements of the Thy-1 gene. EMBO J 9: 833–840

    Google Scholar 

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Sumi-Ichinose, C., Hasegawa, S., Ohtsuki, M. et al. Analysis of an alternative promoter that regulates tissue-specific expression of the human aromatic L-amino acid decarboxylase gene in cultured cell lines. J. Neural Transmission 103, 1–15 (1996). https://doi.org/10.1007/BF01292612

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  • DOI: https://doi.org/10.1007/BF01292612

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