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巴顿病基因CLN3的基因组结构和完整核苷酸序列

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

作者信息

Mitchison H M, Munroe P B, O'Rawe A M, Taschner P E, de Vos N, Kremmidiotis G, Lensink I, Munk A C, D'Arigo K L, Anderson J W, Lerner T J, Moyzis R K, Callen D F, Breuning M H, Doggett N A, Gardiner R M, Mole S E

机构信息

Department of Paediatrics, University College London Medical School, Rayne Institute, United Kingdom.

出版信息

Genomics. 1997 Mar 1;40(2):346-50. doi: 10.1006/geno.1996.4576.

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.

摘要

我们最近克隆了CLN3的cDNA,CLN3是青少年型神经元蜡样脂褐质沉积症(又称巴滕病)的致病基因。为解析其基因组结构,我们使用了一个包含CLN3的黏粒克隆,除已发表的CLN3 cDNA起始位点上游1.1 kb和聚腺苷酸化位点下游0.3 kb外,对整个基因进行了测序。CLN3至少由15个外显子组成,跨度为15 kb,大小从47至356 bp不等。14个内含子大小从80至4227 bp不等,所有外显子/内含子连接序列均符合GT/AG规则。内含子以及5'和3'非翻译区内存在大量重复性Alu元件。CLN3基因的5'区域包含几个潜在的转录调控元件,但未发现共有TATA-1框。CLN3与27个已提交的人类EST同源,序列比较表明该基因存在可变剪接,且在已发表的CLN3 cDNA起始位点上游存在转录序列。

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