大鼠多囊肾病1基因的组织特异性表达和剪接

Hui Xu, Jianjun Shen, C. Walker, E. Kleymenova
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引用次数: 11

摘要

常染色体显性多囊肾病(ADPKD)是最常见的遗传性潜在致命性人类疾病,多囊肾病1 (Pkdl)基因占这些病例的85-90%。我们获得了大鼠Pkdl cDNA序列,并对正常大鼠组织中Pkdl RNA转录物的剪接进行了表征。我们的序列数据揭示了Pkdl基因在大鼠和其他物种之间的高度保守性,并将大鼠Pkdl定位在10号染色体上,以“尾对尾”的方向定位到结节性硬化症2 (Tsc2)基因。发现Pkdl在正常大鼠组织中普遍表达,并且大脑具有复杂的外显子12剪接模式。研究人员还发现了一种缺乏整个外显子31的新型剪接变体,这种变体在大鼠和小鼠中存在,但在人类中不存在。由于大鼠似乎是研究多囊肾疾病的有价值的模型,大鼠Pkdl基因的表征将有助于进一步研究多囊肾动物模型中囊发生的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue-specific Expression and Splicing of the Rat Polycystic Kidney Disease 1 Gene
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic potentially lethal human disorder and the polycystic kidney disease 1 (Pkdl) gene is accounted for 85-90% of these cases. We have obtained rat Pkdl cDNA sequence and characterized splicing of Pkdl RNA transcripts in normal rat tissues. Our sequence data revealed a high conservation of the Pkdl gene between rat and other species and mapped rat Pkdl to chromosome 10 in “tail-to-tail” orientation to the tuberous sclerosis 2 (Tsc2) gene. Pkdl was found ubiquitously expressed in the normal rat tissues and the brain had a complex pattern of exon 12 splicing. A novel splicing variant lacking entire exon 31, which occurs in rat and mouse but not in humans, was also identified. As the rat appears to be a valuable model for investigating polycystic kidney disease, the characterization of the rat Pkdl gene will help facilitate future studies to elucidate the molecular mechanisms of cystogenesis in this animal model.
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