人蛋白磷酸酶抑制剂2在乳腺血管化肿瘤中异构体cDNA的克隆

I. Wu, Marsha A. Mosesx
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引用次数: 3

摘要

利用改进的差异显示,一个基因片段被确定为在人血管化乳腺癌中过度表达,与邻近的正常组织相比。通过定量RT-PCR证实差异表达模式。用3′端RACE和5′端RACE分别克隆全长cDNA。对该基因全长cDNA的分析表明,该基因编码一个615 bp的开放阅读框,与人类蛋白磷酸酶抑制剂-2高度同源,在核苷酸水平上同源性为92%,在氨基酸水平上同源性为89%。本研究结果表明,这种新的人类蛋白磷酸酶抑制剂-2 (nPPI-2)亚型可能参与乳腺肿瘤发展过程中的血管生成开关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning of a cDNA Encoding an Isoform of Human Protein Phosphatase Inhibitor 2 from Vascularized Breast Tumor
Using modified differential display, a gene fragment was identified as being over-expressed in human vascularized breast carcinoma when compare to its neighboring normal tissue. The differentially expressed pattern was confirmed by quantitative RT-PCR. Full-length cDNA was then cloned by both 3′-end RACE and 5′-end RACE. Analysis of the full-length cDNA of this gene reveals that this cDNA encodes an open reading frame of 615 bp, which is highly homologous to human protein phosphatase inhibitor-2, with 92% identity at the nucleotide level, and 89% identity at amino acid level. The results of this study suggest that this novel isoform of human protein phosphatase inhibitor-2 (nPPI-2) may be involved in the angiogenic switch during breast tumor development.
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