首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Molecular cloning sequencing tissue distribution and functional expression of a Na+/H+ exchanger (NHE-2).
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Molecular cloning sequencing tissue distribution and functional expression of a Na+/H+ exchanger (NHE-2).

机译:Na + / H +交换子(NHE-2)的分子克隆测序组织分布和功能表达。

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摘要

The present studies demonstrate cloning, sequencing, tissue distribution, and functional expression of a Na+/H+ exchanger which was isolated from a rat intestinal cDNA library. The cloned cDNA recognizes two transcripts in poly(A)+ RNA from the stomach, jejunum, ileum, liver, large intestine, and uterus. Based on deduced amino acid sequences, this clone shares sequence homology with the other known Na+/H+ exchanger isoforms (NHE-1, NHE-3, and NHE-4) except for its 5' end. Overall, the protein exhibits 47.8%, 41.2%, and 56.2% amino acid sequence identity to NHE-1, NHE-3, and NHE-4, respectively. The hydropathy profile of the predicted protein shows 10 transmembrane domains, suggesting a protein with transport characteristics. The tissue distribution differs from that of the other Na+/H+ exchanger isoforms. The cDNA hybridizes to two closely related transcripts in the mRNA of these tissues, which suggests that the predominant transcript of this clone is alternatively spliced. Transfection of this cDNA into Na+/H+ exchanger-deficient mutant fibroblasts (PS120 cells) results in functional Na+/H+ exchange activity. These data suggest that we have cloned a member of the Na+/H+ exchanger family with tissue-specific expression. We suggest the designation of NHE-2 for this Na+/H+ exchanger.
机译:本研究表明从大鼠肠道cDNA文库中分离出的Na + / H +交换子的克隆,测序,组织分布和功能表达。克隆的cDNA从胃,空肠,回肠,肝脏,大肠和子宫中识别poly(A)+ RNA中的两个转录本。基于推导的氨基酸序列,此克隆与其他已知的Na + / H +交换异构体(NHE-1,NHE-3和NHE-4)具有5'端相同的序列同源性。总体而言,该蛋白质与NHE-1,NHE-3和NHE-4分别具有47.8%,41.2%和56.2%的氨基酸序列同一性。预测蛋白的亲水性谱显示10个跨膜结构域,表明该蛋白具有转运特性。组织分布不同于其他Na + / H +交换异构体。 cDNA与这些组织的mRNA中的两个紧密相关的转录物杂交,这表明该克隆的主要转录物被剪接。将此cDNA转染到Na + / H +交换子不足的突变成纤维细胞(PS120细胞)中会导致功能性的Na + / H +交换活性。这些数据表明我们已经克隆了具有组织特异性表达的Na + / H +交换子家族的成员。我们建议为此Na + / H +交换剂指定NHE-2。

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