Xu Zhi-Gang, Du Jian-Jun, Zhang Xin, Cheng Zhi-Hong, Ma Zhen-Zhong, Xiao Hua-Sheng, Yu Li, Wang Zhi-Qin, Li Yu-Yang, Huo Ke-Ke, Han Ze-Guang
Chinese National Human Genome Center at Shanghai, Shanghai, China.
Hepatology. 2003 Sep;38(3):735-44. doi: 10.1053/jhep.2003.50340.
We currently identified a liver-specific gene that encodes a novel zona pellucida (ZP) domain-containing protein named liver-specific ZP domain-containing protein (LZP). The full-length complementary DNA (cDNA) of human LZP has 2,255 bp with a complete open reading frame (ORF) of 1,635 bp. The gene is localized on chromosome 10q21.3 and spans 40 kb with 9 encoding exons and 8 introns. The deduced protein sequence has 545 amino acid residues, with an N-terminal signal peptide followed by 3 epidermal growth factor (EGF)-like domains and a ZP domain in C-terminal section. Interestingly, human LZP is expressed specifically in liver out of 23 tissues examined, and its mouse counterpart was detected at very early stage during embryo development. Moreover, LZP can be secreted into blood, albeit the protein was localized mainly on the nuclear envelop of hepatocytes. Most importantly, LZP is down-regulated in hepatocellular carcinoma (HCC) and HCC cell lines; meanwhile, the decreased level of hLZP messenger RNA (mRNA) could, at least in some HCC samples, be related to the methylation status of the putative LZP promoter. However, overexpression of hLZP in HCC cell line SMMC-7721 and human liver cell line L02 by stable cell transfection did not inhibit cell growth, implying that the down-regulation of hLZP in HCC might be a consequence of the dedifferentiation involved in hepatocarcinogenesis. In conclusion, these data suggest that LZP is a liver-specific protein involved possibly in hepatocellular function and development, and the protein could be used as potential negative biomarker for HCC pathologic diagnosis.
我们目前鉴定出一种肝脏特异性基因,该基因编码一种名为肝脏特异性含透明带(ZP)结构域蛋白(LZP)的新型含ZP结构域蛋白。人LZP的全长互补DNA(cDNA)为2255 bp,具有1635 bp的完整开放阅读框(ORF)。该基因定位于10号染色体q21.3,跨度为40 kb,有9个编码外显子和8个内含子。推导的蛋白质序列有545个氨基酸残基,N端有信号肽,随后是3个表皮生长因子(EGF)样结构域,C端有一个ZP结构域。有趣的是,在所检测的23种组织中,人LZP仅在肝脏中特异性表达,其小鼠同源物在胚胎发育的早期阶段即可检测到。此外,LZP可分泌到血液中,尽管该蛋白主要定位于肝细胞的核膜上。最重要的是,LZP在肝细胞癌(HCC)及HCC细胞系中表达下调;同时,在至少一些HCC样本中,hLZP信使核糖核酸(mRNA)水平的降低可能与假定的LZP启动子的甲基化状态有关。然而,通过稳定细胞转染在HCC细胞系SMMC-7721和人肝细胞系L02中过表达hLZP并未抑制细胞生长,这意味着HCC中hLZP的下调可能是肝癌发生过程中去分化的结果。总之,这些数据表明LZP是一种肝脏特异性蛋白,可能参与肝细胞功能和发育,该蛋白可作为HCC病理诊断的潜在阴性生物标志物。