Human type-1 angiotensin II (AT1) receptor gene structure and function.

K M Curnow
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Abstract

1. The type-1 angiotensin II (AngII) receptors, designated AT1, mediate most of the biological actions of the peptide hormone AngII. They are the most recent drug target for the treatment of hypertension and cardiac failure and basic research is now focusing on the mechanisms that regulate their expression. 2. In humans there is a single AT1 gene. It encodes a 47 kb pre-mRNA containing five exons, with the previously described AT1 open reading frame (ORF) on exon 5. Alternative splicing results in the production of mature mRNA that are translated at different efficiencies and encode two receptor isoforms. The inclusion of exon 2 markedly inhibits translation of the down-stream ORF, both in vitro and in vivo. Nonetheless, this exon is present in up to one-half of AT1 mRNA in all tissues studied. 3. Transcripts containing exon 3 spliced to exon 5 encode a receptor with an amino-terminal extension of 32 amino acids and represent up to one-third of total AT1 mRNA in each tissue examined. In vitro, these latter transcripts are translated to produce a longer receptor and, in transfected cells, they encode a functional AT1 receptor with ligand-binding and signalling properties similar to those of the short isoform. 4. Exon 4 is of minor significance as it is rarely spliced into AT1 mRNA. 5. These data indicate that, in addition to characterizing factors that modulate AT1 promoter activity and RNA stability, it is important to analyse the splicing patterns of this gene when studying the regulation of its expression.

人类 1 型血管紧张素 II(AT1)受体基因的结构和功能。
1.1型血管紧张素II(AngII)受体(AT1)介导了肽类激素AngII的大部分生物作用。它们是治疗高血压和心力衰竭的最新药物靶点,目前基础研究的重点是调节其表达的机制。2.人类只有一个 AT1 基因。它编码一个 47 kb 的前核糖核酸,包含 5 个外显子,先前描述的 AT1 开放阅读框(ORF)位于第 5 号外显子上。交替剪接产生的成熟 mRNA 翻译效率不同,并编码两种受体异构体。外显子 2 的加入明显抑制了下游 ORF 的体外和体内翻译。然而,在研究的所有组织中,高达二分之一的 AT1 mRNA 都含有该外显子。3.3. 含有外显子 3 并与外显子 5 拼接的转录本编码的受体具有 32 个氨基酸的氨基末端延伸,在所研究的各组织中占 AT1 mRNA 总量的三分之一。在体外,这些后一种转录本经翻译后产生一种较长的受体,在转染细胞中,它们编码一种功能性 AT1 受体,其配体结合和信号特性与短异构体相似。4.外显子 4 意义不大,因为它很少被剪接到 AT1 mRNA 中。5.5. 这些数据表明,在研究 AT1 基因的表达调控时,除了确定调节 AT1 启动子活性和 RNA 稳定性的因素外,分析该基因的剪接模式也很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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