Transcriptional regulation of myelin associated glycoprotein gene expression by cyclic AMP

P. Ye, I. Laszkiewicz, R. C. Wiggins, G. W. Konat

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The treatment of rat glioma C6 cells with 10μ isoproterenol (Ipt) for 4 days upregulated the expression of the myelin‐associated glycoprotein (MAG) gene by approximately 55‐fold over the control value. The constant presence of Ipt in the medium was required for the maximal upregulation, as time‐restricted exposures to the drug produced only partial, or no upregulation of the gene. No difference in the MAG mRNA stability could be detected in Ipt‐treated vs untreated cells indicating that the drug upregulates the MAG gene at transcriptional level. Serum (FCS) strongly attenuated the response of the MAG gene to Ipt. The stimulatory effect of Ipt was profoundly reduced by supermine and H‐89, indicating that protein kinase A‐dependent protein phosphorylation is involved in the MAG gene activation. Within 30 min after Ipt administration, the c‐fos gene was upregulated by 10‐fold, and thereafter, its message level decreased and stabilized at approximately 3‐fold over control. In contrast, the c‐jun gene was downregulated to approximately 20% of control within 30 min after Ipt administration. Subsequently, its message level rose and fell once again within 12 h to approximately half of control, and returned to control level within 72 h. Transfection of C6 cells with progressively deleted pCAT constructs containing up to 861 bp of the MAG gene upstream region demonstrated that active core promoter of the gene is located within 138 bp upstream from the initiation start site. Additional sequences contain both activating and repressive cis‐elements. Practically no upregulation of the CAT activity could be elicited by challenging the transfected cells with Ipt, indicating that AP‐1 sites (14 within the 861 bp region) are not solely responsible for the Ipt‐induced upregulation of the MAG gene, and that the responsible cis‐elements map further upstream from the transcriptional unit. Wiley‐Liss, Inc.

Original languageEnglish (US)
Pages (from-to)683-690
Number of pages8
JournalJournal of Neuroscience Research
Volume37
Issue number6
DOIs
StatePublished - Apr 15 1994

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Myelin-Associated Glycoprotein
Cyclic AMP
Isoproterenol
Gene Expression
Glycoproteins
Genes
Up-Regulation
RNA Stability
Glioma
Pharmaceutical Preparations
Protein Kinases
Transcriptional Activation
Transfection
Down-Regulation
Phosphorylation

All Science Journal Classification (ASJC) codes

  • Cellular and Molecular Neuroscience

Cite this

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title = "Transcriptional regulation of myelin associated glycoprotein gene expression by cyclic AMP",
abstract = "The treatment of rat glioma C6 cells with 10μ isoproterenol (Ipt) for 4 days upregulated the expression of the myelin‐associated glycoprotein (MAG) gene by approximately 55‐fold over the control value. The constant presence of Ipt in the medium was required for the maximal upregulation, as time‐restricted exposures to the drug produced only partial, or no upregulation of the gene. No difference in the MAG mRNA stability could be detected in Ipt‐treated vs untreated cells indicating that the drug upregulates the MAG gene at transcriptional level. Serum (FCS) strongly attenuated the response of the MAG gene to Ipt. The stimulatory effect of Ipt was profoundly reduced by supermine and H‐89, indicating that protein kinase A‐dependent protein phosphorylation is involved in the MAG gene activation. Within 30 min after Ipt administration, the c‐fos gene was upregulated by 10‐fold, and thereafter, its message level decreased and stabilized at approximately 3‐fold over control. In contrast, the c‐jun gene was downregulated to approximately 20{\%} of control within 30 min after Ipt administration. Subsequently, its message level rose and fell once again within 12 h to approximately half of control, and returned to control level within 72 h. Transfection of C6 cells with progressively deleted pCAT constructs containing up to 861 bp of the MAG gene upstream region demonstrated that active core promoter of the gene is located within 138 bp upstream from the initiation start site. Additional sequences contain both activating and repressive cis‐elements. Practically no upregulation of the CAT activity could be elicited by challenging the transfected cells with Ipt, indicating that AP‐1 sites (14 within the 861 bp region) are not solely responsible for the Ipt‐induced upregulation of the MAG gene, and that the responsible cis‐elements map further upstream from the transcriptional unit. Wiley‐Liss, Inc.",
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Transcriptional regulation of myelin associated glycoprotein gene expression by cyclic AMP. / Ye, P.; Laszkiewicz, I.; Wiggins, R. C.; Konat, G. W.

In: Journal of Neuroscience Research, Vol. 37, No. 6, 15.04.1994, p. 683-690.

Research output: Contribution to journalArticle

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T1 - Transcriptional regulation of myelin associated glycoprotein gene expression by cyclic AMP

AU - Ye, P.

AU - Laszkiewicz, I.

AU - Wiggins, R. C.

AU - Konat, G. W.

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N2 - The treatment of rat glioma C6 cells with 10μ isoproterenol (Ipt) for 4 days upregulated the expression of the myelin‐associated glycoprotein (MAG) gene by approximately 55‐fold over the control value. The constant presence of Ipt in the medium was required for the maximal upregulation, as time‐restricted exposures to the drug produced only partial, or no upregulation of the gene. No difference in the MAG mRNA stability could be detected in Ipt‐treated vs untreated cells indicating that the drug upregulates the MAG gene at transcriptional level. Serum (FCS) strongly attenuated the response of the MAG gene to Ipt. The stimulatory effect of Ipt was profoundly reduced by supermine and H‐89, indicating that protein kinase A‐dependent protein phosphorylation is involved in the MAG gene activation. Within 30 min after Ipt administration, the c‐fos gene was upregulated by 10‐fold, and thereafter, its message level decreased and stabilized at approximately 3‐fold over control. In contrast, the c‐jun gene was downregulated to approximately 20% of control within 30 min after Ipt administration. Subsequently, its message level rose and fell once again within 12 h to approximately half of control, and returned to control level within 72 h. Transfection of C6 cells with progressively deleted pCAT constructs containing up to 861 bp of the MAG gene upstream region demonstrated that active core promoter of the gene is located within 138 bp upstream from the initiation start site. Additional sequences contain both activating and repressive cis‐elements. Practically no upregulation of the CAT activity could be elicited by challenging the transfected cells with Ipt, indicating that AP‐1 sites (14 within the 861 bp region) are not solely responsible for the Ipt‐induced upregulation of the MAG gene, and that the responsible cis‐elements map further upstream from the transcriptional unit. Wiley‐Liss, Inc.

AB - The treatment of rat glioma C6 cells with 10μ isoproterenol (Ipt) for 4 days upregulated the expression of the myelin‐associated glycoprotein (MAG) gene by approximately 55‐fold over the control value. The constant presence of Ipt in the medium was required for the maximal upregulation, as time‐restricted exposures to the drug produced only partial, or no upregulation of the gene. No difference in the MAG mRNA stability could be detected in Ipt‐treated vs untreated cells indicating that the drug upregulates the MAG gene at transcriptional level. Serum (FCS) strongly attenuated the response of the MAG gene to Ipt. The stimulatory effect of Ipt was profoundly reduced by supermine and H‐89, indicating that protein kinase A‐dependent protein phosphorylation is involved in the MAG gene activation. Within 30 min after Ipt administration, the c‐fos gene was upregulated by 10‐fold, and thereafter, its message level decreased and stabilized at approximately 3‐fold over control. In contrast, the c‐jun gene was downregulated to approximately 20% of control within 30 min after Ipt administration. Subsequently, its message level rose and fell once again within 12 h to approximately half of control, and returned to control level within 72 h. Transfection of C6 cells with progressively deleted pCAT constructs containing up to 861 bp of the MAG gene upstream region demonstrated that active core promoter of the gene is located within 138 bp upstream from the initiation start site. Additional sequences contain both activating and repressive cis‐elements. Practically no upregulation of the CAT activity could be elicited by challenging the transfected cells with Ipt, indicating that AP‐1 sites (14 within the 861 bp region) are not solely responsible for the Ipt‐induced upregulation of the MAG gene, and that the responsible cis‐elements map further upstream from the transcriptional unit. Wiley‐Liss, Inc.

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