Inazu Tetsuya, Kuroiwa Asato, Matsuda Yoichi, Miyamoto Kaoru
Department of Biochemistry, Fukui Medical University, Matsuoka, Fukui, Japan.
Mol Biol Rep. 2005 Mar;32(1):35-40. doi: 10.1007/s11033-004-4747-x.
We report the isolation of human pleckstrin 2 cDNA. The cDNA contains a 1059 bp open reading frame encoding a polypeptide of 353 amino acid residues. The deduced amino acid sequence indicates that pleckstrin 2 contains two pleckstrin homology domains and a DEP (dishvelled, egl-10, and pleckstrin) domain and had a 95% identity with the sequence of mouse pleckstrin 2. Northern blot and a reverse transcription-coupled polymerase chain reaction analysis revealed that pleckstrin 2 mRNA is widely expressed in a variety of cell lines. The chromosomal location of the mouse pleckstrin 2 gene was on the D3 band of chromosome 12, as determined by fluorescence in situ hybridization and the human pleckstrin 2 gene was mapped to chromosome 14q24.1 by a bioinformatics analysis.
我们报道了人pleckstrin 2 cDNA的分离。该cDNA包含一个1059 bp的开放阅读框,编码一个由353个氨基酸残基组成的多肽。推导的氨基酸序列表明,pleckstrin 2包含两个pleckstrin同源结构域和一个DEP(散乱蛋白、egl-10和pleckstrin)结构域,并且与小鼠pleckstrin 2的序列具有95%的同一性。Northern印迹和逆转录偶联聚合酶链反应分析显示,pleckstrin 2 mRNA在多种细胞系中广泛表达。通过荧光原位杂交确定,小鼠pleckstrin 2基因的染色体定位在12号染色体的D3带,通过生物信息学分析将人pleckstrin 2基因定位于14q24.1染色体。