首页> 外文期刊>Biochimica et biophysica acta. Molecular basis of disease: BBA >The mouse N-acetylgalactosamine-6-sulfate sulfatase (Galns) gene: cDNA isolation, genomic characterization, chromosomal assignment and analysis of the 5'-flanking region
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The mouse N-acetylgalactosamine-6-sulfate sulfatase (Galns) gene: cDNA isolation, genomic characterization, chromosomal assignment and analysis of the 5'-flanking region

机译:小鼠N-乙酰半乳糖胺-6-硫酸盐硫酸酯酶(Galns)基因:cDNA分离,基因组表征,染色体分配和5'侧翼区分析

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Deficiency of lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS) leads to mucopolysaccharidosis IV A (MPS IV A), for which there is no definitive treatment so far. Although a number of nutations of the GALNS gene of MPS IV A patients have been described, pathogenesis of the disorder still remains elusive. In order to facilitate in vivo studies using model animals for MPS IV A, we isolated and performed molecular characterization of the mouse homolog of human GALNS. The 2.3-kb cDNA contains a 1560-bp open reading frame encoding 520 amino acid residues. The coding region has 84% similarity to the human GALNS cDNA at amino acid level. The mouse Galns gene was mapped by interspecific backcross analysis to the distal region of chromosome 8 where it co-segregates with Aprt. Northern blot analysis showed a wide expression of a single-copy gene, being higher especially in liver and kidney. The Galns gene was isolated from S129vJ genomic library and its genomic organization was characterized. The mouse Galns gene was about 50-kb long and organized into 14 exons and 13 introns. All intron-exon splice junctions conformed to the GT/AG consensus sequence except exon 8/intron 8 junction. Primer extension shows multiple transcription initiation sites between -44 and -75 although major transcription initiation site was observed at -90 bp from the ATG codon. The 5'-flanking region lacks canonical TATA and CAAT box sequences, but is G+C rich with 10 GC boxes (potential Sp1 binding sites), characteristic of a housekeeping gene promoter.
机译:溶酶体酶N-乙酰半乳糖胺-6-硫酸盐硫酸酯酶(GALNS)的缺乏会导致粘多糖贮积症IV A(MPS IV A),目前尚无确定的治疗方法。尽管已经描述了MPS IV A患者的GALNS基因的许多失调,但该疾病的发病机理仍然难以捉摸。为了促进使用MPS IV A模型动物的体内研究,我们分离并进行了人GALNS小鼠同源物的分子表征。 2.3kb的cDNA含有1560bp的开放阅读框,编码520个氨基酸残基。编码区在氨基酸水平上与人GALNS cDNA有84%的相似性。通过种间回交分析将小鼠Galns基因定位到8号染色体的远端区域,在该区域与Aprt共分离。 Northern印迹分析显示单拷贝基因的广泛表达,尤其在肝脏和肾脏中更高。从S129vJ基因组文库中分离出Galns基因,并对其基因组结构进行了表征。小鼠Galns基因长约50kb,并组织成14个外显子和13个内含子。除外显子8 /内含子8接头外,所有内含子-外显子剪接接头均符合GT / AG共有序列。引物延伸显示在-44和-75之间的多个转录起始位点,尽管在距ATG密码子-90 bp处观察到了主要的转录起始位点。 5'侧翼区域缺乏规范的TATA和CAAT框序列,但是富含G + C,具有10个GC框(潜在的Sp1结合位点),这是管家基因启动子的特征。

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