GFAP beta mRNA is an alternative transcript of the glial fibrillary acidic protein (GFAP) gene, whose transcriptional start site is located 169 nucleotides upstream to the classical GFAP alpha mRNA. By an RT-PCR method with primers on separate exons, we were able to confirm the presence of GFAP transcripts with a longer 5' untraslated region in all the examined areas of rat brain and in primary cultures of astroglial cells. Northern blot analysis, using an oligoprobe specific for the 5' region of GFAP beta, revealed a single hybridization band of 2.9 kb in all the brain regions examined and in primary cultures of astroglial cells. The availability of the quantitative Northern blot assay allowed further studies on the regulation of GFAP beta expression in vivo. Since it is well-known that neuronal brain injury is one of the most powerful inducers of GFAP, we examined the expression of GFAP alpha and beta after a neurotoxic lesion in the rat hippocampus. Results obtained show a parallel increase in both GFAP transcripts with an identical time-course, suggesting that regulatory regions of the gene influence in similar way the rate transcription at the two different start sites (alpha and beta) or that a similar post-transcriptional mechanism is involved in regulating both mRNA isoforms.

GFAP beta mRNA expression in the normal rat brain and after neuronal injury / Condorelli, Df; Nicoletti, Vg; Dell'Albani, P; Barresi, V; Caruso, Alessandra Sebastiana Maria; Conticello, Sg; Belluardo, N; Giuffrida, Stella. - In: NEUROCHEMICAL RESEARCH. - ISSN 0364-3190. - 24:(1999), pp. 709-714. [10.1023/A:1021016828704]

GFAP beta mRNA expression in the normal rat brain and after neuronal injury

CARUSO, Alessandra Sebastiana Maria;
1999

Abstract

GFAP beta mRNA is an alternative transcript of the glial fibrillary acidic protein (GFAP) gene, whose transcriptional start site is located 169 nucleotides upstream to the classical GFAP alpha mRNA. By an RT-PCR method with primers on separate exons, we were able to confirm the presence of GFAP transcripts with a longer 5' untraslated region in all the examined areas of rat brain and in primary cultures of astroglial cells. Northern blot analysis, using an oligoprobe specific for the 5' region of GFAP beta, revealed a single hybridization band of 2.9 kb in all the brain regions examined and in primary cultures of astroglial cells. The availability of the quantitative Northern blot assay allowed further studies on the regulation of GFAP beta expression in vivo. Since it is well-known that neuronal brain injury is one of the most powerful inducers of GFAP, we examined the expression of GFAP alpha and beta after a neurotoxic lesion in the rat hippocampus. Results obtained show a parallel increase in both GFAP transcripts with an identical time-course, suggesting that regulatory regions of the gene influence in similar way the rate transcription at the two different start sites (alpha and beta) or that a similar post-transcriptional mechanism is involved in regulating both mRNA isoforms.
1999
01 Pubblicazione su rivista::01a Articolo in rivista
GFAP beta mRNA expression in the normal rat brain and after neuronal injury / Condorelli, Df; Nicoletti, Vg; Dell'Albani, P; Barresi, V; Caruso, Alessandra Sebastiana Maria; Conticello, Sg; Belluardo, N; Giuffrida, Stella. - In: NEUROCHEMICAL RESEARCH. - ISSN 0364-3190. - 24:(1999), pp. 709-714. [10.1023/A:1021016828704]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/143501
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