两种大鼠Na+/Pi共转运蛋白的分子克隆:转录本差异组织表达的证据。

H Li, Z Xie
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引用次数: 0

摘要

近年来,Na+/Pi共转运活性在大鼠肝细胞中得到证实。在这里,我们报道了从大鼠肝脏cDNA文库中分离到两个Na+/Pi共转运体cDNA (RNaPi-1a和RNaPi-1b)。这两种cdna具有相同的编码,但不同的5'-非翻译区。大鼠cdna编码465个氨基酸的多肽,分别与兔NaPi-1和人肾Na+/Pi共转运蛋白具有62%和66%的一致性。Northern blot分析显示,RNaPi-1a特异性探针检测到两个主要转录本(2.3和1.8 kb),而RNaPi-1b特异性探针在原代培养的大鼠肾、肝和肝细胞中只检测到一个转录本(1.8 kb)。大鼠肝脏的RNaPi-1a表达水平远高于RNaPi-1b,而大鼠肾脏的RNaPi-1b表达水平则相反。在大鼠心脏、大脑和骨骼肌中也检测到低水平的RNaPi-1 mrna。这些发现表明,至少有两种RNaPi-1转录物在肝脏和肾脏中表达,并且RNaPi-1a和RNaPi-1b的表达水平可能受到组织特异性因素的控制。
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Molecular cloning of two rat Na+/Pi cotransporters: evidence for differential tissue expression of transcripts.

Recently, Na+/Pi cotransport activity has been demonstrated in rat liver hepatocytes. Here, we report the isolation of two Na+/Pi cotransporter cDNAs (RNaPi-1a and RNaPi-1b) from a rat liver cDNA library. The two cDNAs have the same coding but different 5'-untranslated regions. The rat cDNAs encode a polypeptide of 465 amino acids, having 62% and 66% identity with the rabbit NaPi-1 and human kidney Na+/Pi cotransporter, respectively. Northern blot analysis showed that a RNaPi-1a--specific probe detected two major transcripts (2.3 and 1.8 kb), whereas a RNaPi-1b--specific probe hybridized with one transcript (1.8 kb) in rat kidney, liver, and hepatocytes in primary culture. Rat liver expressed much higher levels of RNaPi-1a than RNaPi-1b, whereas the converse was true for rat kidney. Low levels of RNaPi-1 mRNAs were also detected in rat heart, brain, and skeletal muscle. These findings indicate that there are at least two isoforms of RNaPi-1 transcripts expressed in liver and kidney and that the levels of expression of the RNaPi-1a and RNaPi-1b may be controlled by tissue-specific factors.

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