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研究笔记:鸡蔗糖酶-异麦芽糖酶cDNA序列的鉴定与分离

Research notes: Identification and isolation of chicken sucrase-isomaltase cDNA sequence.

作者信息

Uni Z

机构信息

Animal Science Department, Faculty of Agriculture, Hebrew University of Jerusalem, Rehovot, Israel.

出版信息

Poult Sci. 1998 Jan;77(1):140-4. doi: 10.1093/ps/77.1.140.

Abstract

The intestinal sucrase-isomaltase (SI) complex is a glycoprotein of the small intestine brush border membrane that plays an important role in the final degradation of carbohydrate. To clone the chicken SI, we employed reverse transcriptase polymerase chain reaction (RT-PCR). Agarose gel electrophoresis of the PCR products exhibited one amplified band of approximately 800 bp. The fragment was extracted from the gel and sequenced. The cDNA sequence of the chicken SI is 786 bp in length and exhibits 99% identity at the nucleotide level to the Homo sapiens SI mRNA. Using our cDNA as a probe, Northern analysis revealed a transcript of approximately 6.0 kb in chicken jejunum and ileum tissues.

摘要

肠蔗糖酶-异麦芽糖酶(SI)复合物是一种位于小肠刷状缘膜的糖蛋白,在碳水化合物的最终降解过程中发挥重要作用。为了克隆鸡的SI,我们采用了逆转录聚合酶链反应(RT-PCR)。PCR产物的琼脂糖凝胶电泳显示出一条约800 bp的扩增条带。从凝胶中提取该片段并进行测序。鸡SI的cDNA序列长度为786 bp,在核苷酸水平上与人类SI mRNA具有99%的同一性。以我们的cDNA为探针,Northern分析显示在鸡空肠和回肠组织中有一条约6.0 kb的转录本。

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