Molecular cloning of a novel PPEF-1 gene variant from a T-cell lymphoblastic lymphoma cell line.

Ping Ho, Ken-Shwo Dai, Hui-Ling Chen
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引用次数: 4

Abstract

To determine if there is a gene variant of protein serine-threonine phosphatase with EF hand (PPEF-1) in T-cell lymphoblastic lymphoma SUP-T1 cell line, both in silico and in vitro approaches were conducted. In silico, a cDNA clone showing similar sequence to PPEF-1 was isolated from the SUP-T1 cDNA library and named PPEF-1V. The full-length of the PPEF-1V cDNA clone is a 2135bp containing a 1503bp open reading frame extending from 188bp to 1690bp, which corresponds to an encoded protein of 501 amino acid residues with a predicted molecular mass of 57.8 kDa. Alignment on both PPEF-1V and PPEF-1 sequences showed that PPEF-1V is a 350bp deletion in the nucleotide sequence of PPEF-1 from 128-477bp and a 152-amino-acid N-terminal deletion in the amino acid sequence of PPEF-1. In vitro, PPEF-1V transcript fragment was only highly expressed in T-cell lymphoblastic lymphoma cell line. In conclusion, the present patent showed that PPEF-1V could be a potential target for diagnosis or treatment of T-cell lymphoblastic lymphoma.

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t淋巴母细胞淋巴瘤细胞系新型PPEF-1基因变异的分子克隆
为了确定在t细胞淋巴母细胞淋巴瘤supt - t1细胞系中是否存在带EF手蛋白丝氨酸-苏氨酸磷酸酶(PPEF-1)基因变异,我们采用了硅法和体外法。从SUP-T1 cDNA文库中分离到与PPEF-1序列相似的cDNA克隆,命名为PPEF-1V。PPEF-1V cDNA克隆全长2135bp,包含一个1503bp的开放阅读框,从188bp延伸至1690bp,与501个氨基酸残基的编码蛋白相对应,预测分子量为57.8 kDa。对PPEF-1V和PPEF-1序列比对表明,PPEF-1V在PPEF-1的核苷酸序列128-477bp中缺失了350bp,在PPEF-1的氨基酸序列n端缺失了152个氨基酸。在体外,PPEF-1V转录片段仅在t淋巴母细胞淋巴瘤细胞系中高表达。总之,本专利表明PPEF-1V可能是诊断或治疗t细胞淋巴母细胞淋巴瘤的潜在靶点。
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