Call K M, Glaser T, Ito C Y, Buckler A J, Pelletier J, Haber D A, Rose E A, Kral A, Yeger H, Lewis W H
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Cell. 1990 Feb 9;60(3):509-20. doi: 10.1016/0092-8674(90)90601-a.
We have isolated a series of genomic and cDNA clones mapping within the boundaries of constitutional and tumor deletions that define the Wilms' tumor locus on human chromosome 11 (band p13). The transcription unit corresponding to these clones spans approximately 50 kb and encodes an mRNA approximately 3 kb long. This mRNA is expressed in a limited range of cell types, predominantly in the kidney and a subset of hematopoietic cells. The polypeptide encoded by this locus has a number of features suggesting a potential role in transcriptional regulation. These include the presence of four zinc finger domains and a region rich in proline and glutamine. The amino acid sequence of the predicted polypeptide shows significant homology to two growth regulated mammalian polypeptides, EGR1 and EGR2. The genetic localization of this gene, its tissue-specific expression, and the function predicted from its sequence lead us to suggest that it represents the 11p13 Wilms' tumor gene.
我们分离出了一系列基因组和cDNA克隆,这些克隆定位于界定人类11号染色体(p13带)上威尔姆斯瘤基因座的先天性和肿瘤性缺失区域内。与这些克隆对应的转录单位跨度约50kb,编码一个约3kb长的mRNA。这种mRNA在有限的细胞类型范围内表达,主要在肾脏和一部分造血细胞中表达。该基因座编码的多肽具有许多表明其在转录调控中可能发挥作用的特征。这些特征包括存在四个锌指结构域以及一个富含脯氨酸和谷氨酰胺的区域。预测多肽的氨基酸序列与两种生长调节的哺乳动物多肽EGR1和EGR2具有显著的同源性。该基因的遗传定位、其组织特异性表达以及从其序列预测的功能,使我们认为它代表11p13威尔姆斯瘤基因。