Structure and organization of the human neuronatin gene
- Case Western Reserve Univ., Detroit, MI (United States)
Neuronatin is a brain-specific human gene that we recently isolated and observed to be selectively expressed during brain development. In this report, the genomic structure and organization of human neuronatin is described. The human gene spans 3973 bases and contains three exons and two introns. Based on primer extension analysis, a single cap site is located 124 bases upstream from the methionine (ATG) initiation codon, is good context, GAACCATGG. The promoter contains a modified TATA box, CATAAA (-27), and a modified CAAT box, GGCGAAT (-59). The 5{prime}- flanking region contains putative transcription factor binding sites for SP-1, AP-2 (two sites), {delta}-subunit, SRE-2, NF-Al, and ETS. In addition, a 21-base sequence highly homologous to the neutral restrictive silence element that governs neuron-specific gene expression is observed at -421. Furthermore, SP-1 and AP-3 binding sites are present in intron 1. All splice donor and acceptor sites conformed to the GT/AG rule. Exon 1 encodes 24 amino acids, exon 2 encodes 27 amino acids, and exon 3 encodes 30 amino acids. At the 3{prime}-end of the gene, the poly(A) signal, AATAAA, poly(A) site, and GT cluster are observed. The neuronatin gene is expressed as two mRNA species, {alpha} and {beta}, generated by alternative splicing. The {alpha}-form contains all three exons, whereas in the {beta}-form, the middle exon has been spliced out. The third nucleotide of all frequently used codons, except threonine, of neuronatin is either G or C, consistent with codon usage expected for Homo sapiens. This information about the structure of the human neuronatin gene will help in understanding the significance of this gene in brain development and human disease. 30 refs., 3 figs.
- OSTI ID:
- 465960
- Journal Information:
- Genomics, Vol. 33, Issue 2; Other Information: PBD: 15 Apr 1996
- Country of Publication:
- United States
- Language:
- English
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