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人心脏中新型质膜Ca(2+) -ATP酶剪接变体的mRNA表达分析与克隆

Analysis of mRNA expression and cloning of a novel plasma membrane Ca(2+)-ATPase splice variant in human heart.

作者信息

Santiago-García J, Mas-Oliva J, Saavedra D, Zarain-Herzberg A

机构信息

Division of Cardiovascular Sciences, St. Boniface General Hospital Research Centre, University of Manitoba, Winnipeg, Canada.

出版信息

Mol Cell Biochem. 1996 Feb 23;155(2):173-82. doi: 10.1007/BF00229314.

Abstract

Four different plasma membrane Ca(2+)-ATPase (PMCA) genes and three sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA) genes have been previously cloned and characterized. In this study we have investigated the expression of the mRNA encoding the various PMCA and SERCA proteins in fetal and adult human heart and placenta by the reverse-transcriptase-polymerase-chain-reaction (RT-PCR) and cDNA cloning. We have found that PMCA1 and PMCA4 genes were expressed in 8-, 12- and 20-week fetal heart and in adult heart. PMCA2 gene was expressed at low levels in adult heart but was not detected in fetal heart. PMCA3 mRNA was not detected in the heart nor placenta. In contrast, the mRNA encoding SERCA2a, SERCA2b and SERCA3 were expressed in all cardiac developmental stages. Multiple alternatively spliced mRNA transcripts which differ at splice site A and B/C of the PMCA1, PMCA2 and PMCA4 genes were detected in the human heart. Interestingly, a novel tissue specific variant of the PMCA4 gene was detected in both fetal and adult human heart but not in placenta that accounts for about 30% of the total PMCA4 mRNA variant expression. DNA sequence analysis of this novel variant revealed that it corresponds to the equivalent of the PMCA1d variant and accordingly we have named it PMCA4d. We cloned and sequenced eight cDNA inserts encoding for the PMCA1 and PMCA4 variants from a fetal human heart cDNA library confirming that these are the two main PMCA genes expressed in cardiac muscle.

摘要

先前已克隆并鉴定出四种不同的质膜钙ATP酶(PMCA)基因和三种肌质(内质)网钙ATP酶(SERCA)基因。在本研究中,我们通过逆转录聚合酶链反应(RT-PCR)和cDNA克隆,研究了编码各种PMCA和SERCA蛋白的mRNA在胎儿及成人心脏和胎盘中的表达情况。我们发现,PMCA1和PMCA4基因在8周、12周和20周的胎儿心脏以及成人心脏中均有表达。PMCA2基因在成人心脏中低水平表达,但在胎儿心脏中未检测到。在心脏和胎盘中均未检测到PMCA3 mRNA。相比之下,编码SERCA2a、SERCA2b和SERCA3的mRNA在所有心脏发育阶段均有表达。在人类心脏中检测到了多个在PMCA1、PMCA2和PMCA4基因的剪接位点A和B/C处存在差异的可变剪接mRNA转录本。有趣的是,在胎儿和成人心脏中均检测到了一种新的PMCA4基因组织特异性变体,但在胎盘中未检测到,该变体约占PMCA4 mRNA变体总表达量的30%。对这种新变体的DNA序列分析表明,它相当于PMCA1d变体,因此我们将其命名为PMCA4d。我们从胎儿人类心脏cDNA文库中克隆并测序了八个编码PMCA1和PMCA4变体的cDNA插入片段,证实这是在心肌中表达的两个主要PMCA基因。

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