Ho Ping, Dai Ken-Shwo, Chen Hui-Ling
Division of General Surgery, Buddhist Tzu Chi General Hospital, Taipei Branch, Taiwan.
Recent Pat DNA Gene Seq. 2012 Apr;6(1):72-7. doi: 10.2174/187221512799303172.
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.
为了确定T细胞淋巴母细胞淋巴瘤SUP-T1细胞系中是否存在含EF手型的蛋白丝氨酸-苏氨酸磷酸酶(PPEF-1)的基因变体,我们采用了计算机模拟和体外实验方法。在计算机模拟方面,从SUP-T1 cDNA文库中分离出一个与PPEF-1序列相似的cDNA克隆,并将其命名为PPEF-1V。PPEF-1V cDNA克隆的全长为2135bp,包含一个从188bp延伸至1690bp的1503bp开放阅读框,对应一个由501个氨基酸残基组成的编码蛋白,预测分子量为57.8 kDa。对PPEF-1V和PPEF-1序列的比对显示,PPEF-1V在PPEF-1核苷酸序列的128 - 477bp处有一个350bp的缺失,在PPEF-1氨基酸序列中有一个152个氨基酸的N端缺失。在体外,PPEF-1V转录片段仅在T细胞淋巴母细胞淋巴瘤细胞系中高表达。总之,本研究表明PPEF-1V可能是T细胞淋巴母细胞淋巴瘤诊断或治疗的潜在靶点。