Predominant expression of human zic in cerebellar granule cell lineage and medulloblastoma.

生物 互补DNA 锌指 分子生物学 小脑 髓母细胞瘤 颗粒细胞 肽序列 同源染色体 基因 遗传学 中枢神经系统 齿状回 转录因子 神经科学
作者
Naoki Yokota,Jun Aruga,Setsuo Takai,Kiyomi Yamada,Minoru Hamazaki,Toshio Iwase,Haruhiko Sugimura,Katsuhiko Mikoshiba
出处
期刊:PubMed [National Institutes of Health]
卷期号:56 (2): 377-83 被引量:99
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Zic is a novel zinc finger protein which displays a highly restricted expression pattern in the adult and developing mouse cerebellum and is highly homologous to the recently cloned Drosophila pair-rule gene Opa. To clarify the mechanism for the development of the human cerebellum and its involvement in human nervous system diseases, we have isolated human Zic cDNA and examined its expression by using monoclonal antibody against recombinant Zic protein. The nucleotide sequence of human Zic cDNA is 85% homologous to that of mouse Zic cDNA. Its putative amino acid sequence is highly conserved (> 99%) except for substitution of only two amino acid residues. In situ chromosome hybridization localized the human Zic gene to chromosome band 3q24. Human Zic protein was immunohistochemically detected in the nuclei of the cerebellar granule cell lineage from the progenitor cells of the external germinal layer to the postmigrated cells of the internal granular layer. Furthermore, Zic protein was detected in medulloblastoma (26/29 cases), whereas no other tumors examined (over 70 cases including primitive neuroectodermal tumors) expressed this protein. These findings suggest that Zic is a potential biomarker for medulloblastoma as well as the human cerebellar granule cell lineage.

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