Sun D S, Chang A C, Jenkins N A, Gilbert D J, Copeland N G, Chang N C
Institute of Microbiology & Immunology, National Yang-Ming University, Taipei, 112, Taiwan.
Genomics. 1996 Aug 15;36(1):54-62. doi: 10.1006/geno.1996.0425.
cDNA clones encoding a novel protein (LUZP) with three leucine zipper motifs were first identified from a murine bone marrow cDNA library. After screening two additional cDNA libraries of activated peritoneal exudate cells, 32 positive clones were obtained from 1.3 x 10(7) phage plaques. Four overlapping clones constituting a total of 7399 bp were sequenced on both strands. The complete open reading frame of LUZP is 1067 amino acids. In addition to three leucine zipper motifs located at the NH2 terminus, there are three nuclear localization signals and a large number of putative Ser/Thr phosphorylation sites. Western blot analyses indicate that LUZP is predominantly expressed in brain, whereas immunocytochemistry data clearly reveal its presence in the nucleus of neurons. Interspecific backcross analyses have mapped Luzp to mouse chromosome 4 in proximity to Gpcr14. Comparative mapping data suggest that the human homolog of Luzp will map to human chromosome 1p36.
首先从小鼠骨髓cDNA文库中鉴定出编码一种具有三个亮氨酸拉链基序的新型蛋白质(LUZP)的cDNA克隆。在筛选另外两个活化腹膜渗出细胞的cDNA文库后,从1.3×10⁷个噬菌体噬菌斑中获得了32个阳性克隆。对构成总共7399 bp的四个重叠克隆进行了双链测序。LUZP的完整开放阅读框为1067个氨基酸。除了位于NH₂末端的三个亮氨酸拉链基序外,还有三个核定位信号和大量假定的Ser/Thr磷酸化位点。蛋白质印迹分析表明,LUZP主要在脑中表达,而免疫细胞化学数据清楚地揭示了它在神经元细胞核中的存在。种间回交分析已将Luzp定位到小鼠4号染色体上靠近Gpcr14的位置。比较定位数据表明,Luzp的人类同源物将定位到人类1号染色体的1p36区域。