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Cell-specific alternative RNA splicing of an FMRFamide gene transcript in the brain.

作者信息

Saunders S E, Kellett E, Bright K, Benjamin P R, Burke J F

机构信息

Sussex Neuroscience Research Centre, School of Biological Sciences, University of Sussex, Brighton, United Kingdom.

出版信息

J Neurosci. 1992 Mar;12(3):1033-9. doi: 10.1523/JNEUROSCI.12-03-01033.1992.

Abstract

Individual neurons synthesize different peptide neurotransmitters and neuromodulators. In general, specificity is achieved by transcriptional regulation of neuropeptide-encoding genes. In Lymnaea, the FMRFamide and GDP/SDPFLRFamide neuropeptides are encoded by separate exons. Here we provide evidence that the two exons are part of the same gene and that in neurons expressing the gene the two exons are spliced onto a common upstream exon encoding a hydrophobic leader sequence. In addition, in situ hybridization data show that there is mutually exclusive cytoplasmic expression of each of the neuropeptide-encoding exons. Thus, differential neuropeptide synthesis is likely to be regulated by an alternative splicing mechanism. The cellular specificity of these splicing events is remarkable and suggests that cell-specific alternative splicing may be of major importance in establishing neuronal diversity in this system.

摘要

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