| Literature DB >> 9119403 |
H M Mitchison1, P B Munroe, A M O'Rawe, P E Taschner, N de Vos, G Kremmidiotis, I Lensink, A C Munk, K L D'Arigo, J W Anderson, T J Lerner, R K Moyzis, D F Callen, M H Breuning, N A Doggett, R M Gardiner, S E Mole.
Abstract
We recently cloned a cDNA for CLN3, the gene for juvenile-onset neuronal ceroid lipofuscinosis or Batten disease. To resolve the genomic organization we used a cosmid clone containing CLN3 to sequence the entire gene in addition to 1.1 kb 5' of the start of the published CLN3 cDNA and 0.3 kb 3' to the polyadenylation site. CLN3 is organized into at least 15 exons spanning 15 kb and ranging from 47 to 356 bp. The 14 introns vary from 80 to 4227 bp, and all exon/intron junction sequences conform to the GT/AG rule. Numerous repetitive Alu elements are present within the introns and 5'- and 3'-untranslated regions. The 5' region of the CLN3 gene contains several potential transcription regulatory elements but no consensus TATA-1 box was identified. CLN3 is homologous to 27 deposited human ESTs, and sequence comparisons suggest alternative splicing of the gene and the existence of transcribed sequences upstream to the start of the published CLN3 cDNA.Entities:
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Year: 1997 PMID: 9119403 DOI: 10.1006/geno.1996.4576
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736