Suppr超能文献

Slc12a2的部分克隆与特性分析:编码分泌型钠-钾-2氯协同转运蛋白的基因

Partial cloning and characterization of Slc12a2: the gene encoding the secretory Na+-K+-2Cl- cotransporter.

作者信息

Randall J, Thorne T, Delpire E

机构信息

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Am J Physiol. 1997 Oct;273(4):C1267-77. doi: 10.1152/ajpcell.1997.273.4.C1267.

Abstract

The Slc12a2 gene encodes a widely expressed bumetanide-sensitive Na+-K+-2Cl- cotransporter that participates in various functions such as Cl- secretion and cell volume regulation. We isolated and characterized 75 kilobases of the murine gene encoding the cotransporter. The cotransport protein is encoded by 27 exons. Ribonuclease protection assay and primer extension demonstrated tissue-specific transcription initiation sites located within 270 base pairs upstream of the start codon. Nucleotide sequence analysis of the proximal 5'-flanking region revealed the presence of a weak TATA box, multiple Sp1/GC consensus sites, and the consensus sequence of a putative transcriptional initiator. Transfection of luciferase reporter gene constructs in mouse inner medullary collecting duct (mIMCD-3) cells confirmed the location of the minimal promoter within a 120-base pair fragment upstream of the cDNA. We also report the identification of an alternatively spliced variant of the cotransporter, expressed primarily in brain. This new spliced variant lacks exon 21, which encodes a 16-amino acid peptide located in the COOH-terminal tail of the protein. The absence of this exon causes the loss of the single protein kinase A consensus site of the cotransport protein.

摘要

Slc12a2基因编码一种广泛表达的布美他尼敏感型钠-钾-2氯共转运体,该共转运体参与多种功能,如氯离子分泌和细胞体积调节。我们分离并鉴定了编码该共转运体的75千碱基的小鼠基因。共转运蛋白由27个外显子编码。核糖核酸酶保护分析和引物延伸表明,组织特异性转录起始位点位于起始密码子上游270个碱基对范围内。对近端5'-侧翼区域的核苷酸序列分析显示存在一个弱TATA框、多个Sp1/GC共有位点以及一个假定转录起始子的共有序列。在小鼠内髓集合管(mIMCD-3)细胞中进行荧光素酶报告基因构建体的转染,证实了最小启动子位于cDNA上游120个碱基对的片段内。我们还报告了共转运体的一种选择性剪接变体的鉴定,该变体主要在脑中表达。这种新的剪接变体缺少外显子21,外显子21编码位于该蛋白COOH末端尾巴中的一个16个氨基酸的肽段。该外显子的缺失导致共转运蛋白的单个蛋白激酶A共有位点丢失。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验