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The major APN transcript of the alveolar type II epithelial cell originates from a unique upstream promoter region

机译:肺泡II型上皮细胞的主要APN转录物来自独特的上游启动子区域

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摘要

Aminopeptidase N (APN, EC 3.4.11.2) is an ectopeptidase expressed in lung at the apical surface of alveolar type II epithelial cells. Its expression is upregulated during fetal lung development. To begin to understand the regulation of APN expression during lung development, we used the rapid modification of cDNA ends (RACE) to clone the 5' end of the major APN transcript in rat lung and alveolar type II cells. The cloned sequence revealed a unique 135 bp untranslated exon which genomic cloning and restriction mapping indicated was located more than 14 kb upstream from the coding sequence. A 172 bp genomic fragment flanking the untranslated exon produced a high level of expression of a reporter gene in transient transfection assays using a human lung adenocarcinoma cell line. The DNA fragment includes elements known to be important for expression of lung specific proteins, inclouding the surfactant-associated proteins A, B, and C and the Clara cell specific protein. Comparison of the APN genomic sequences and gene structure from human and rat suggests that the exon present in the rat lung transcript may result from the use of a previously uncharacterized APN promoter.
机译:氨肽酶N(APN,EC 3.4.11.2)是在肺中表达的肺泡Ⅱ型上皮细胞顶表面的一种肽肽酶。在胎儿肺发育过程中其表达上调。为了开始了解肺发育过程中APN表达的调控,我们使用了cDNA末端的快速修饰(RACE)在大鼠肺和II型肺泡细胞中克隆了主要APN转录本的5'末端。克隆的序列揭示了一个独特的135 bp非翻译外显子,其基因组克隆和限制性酶切图谱表明该序列位于编码序列上游14 kb以上。在使用人肺腺癌细胞系的瞬时转染测定中,未翻译外显子侧翼的172 bp基因组片段产生了高水平的报告基因表达。该DNA片段包括已知对肺特异性蛋白表达很重要的元素,使与表面活性剂相关的蛋白A,B和C以及克拉拉细胞特异性蛋白浑浊。来自人和大鼠的APN基因组序列和基因结构的比较表明,存在于大鼠肺转录物中的外显子可能是由于使用先前未表征的APN启动子而引起的。

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