Hewitt J A, Kessler P M, Campbell C E, Williams B R
Department of Cancer Biology, Cleveland Clinic Foundation, Ohio 44195, USA.
Med Pediatr Oncol. 1996 Nov;27(5):456-61. doi: 10.1002/(SICI)1096-911X(199611)27:5<456::AID-MPO12>3.0.CO;2-8.
The 11p13 Wilms' tumor locus consists of two coordinately regulated transcripts, WT1 and WIT-1. These genes are highly expressed in the developing urogenital system, beginning with the urogenital ridge at day 10.5, the metanephric blastema at day 11.5, and during glomerular formation at day 13.5, becoming ultimately restricted to the podocytes. Stromal cells of the gonad also show abundant expression. WT1 is expressed at lower levels in spleen, uterus, mesothelial linings of organs in the abdominal and thoracic cavities, and the ependymal layer of the ventral aspect of the spinal cord. WIT-1 mRNA is about 10-fold less abundant than WT1, but appears to be expressed in the same tissue-restricted manner. Expression of the WT1 protein is required for kidney development, although its physiological function remains to be determined. The function of WIT-1 is similarly unknown but one intriguing possibility is that it is an antisense regulator of WT1. An understanding of events controlling spatial and temporal regulation of these genes will greatly improve our ability to study the role of WT1 and WIT-1 in urogenital development. We have found that while chimeric reporter constructs containing 0.6-2.5 kb of the 5' region of the WT1 gene direct transcription in many different cell lines, we were unable to detect expression in 13.5-day mouse embryos. However, a cosmid containing about 42 kb encompassing this region was able to direct the expression of abundant levels of mRNA from the appropriate transcription initiation sites in both stable transfectants of mouse Leydig cells (TM3) or in transgenic embryos. We are currently localizing the DNA elements required for this expression.
11p13肾母细胞瘤基因座由两个协同调节的转录本WT1和WIT-1组成。这些基因在泌尿生殖系统发育过程中高度表达,从第10.5天的泌尿生殖嵴开始,到第11.5天的后肾胚芽,以及第13.5天肾小球形成期间,最终局限于足细胞。性腺的基质细胞也有丰富的表达。WT1在脾脏、子宫、腹腔和胸腔器官的间皮衬里以及脊髓腹侧的室管膜层中表达水平较低。WIT-1 mRNA的丰度比WT1低约10倍,但似乎以相同的组织限制性方式表达。WT1蛋白的表达是肾脏发育所必需的,但其生理功能仍有待确定。WIT-1的功能同样未知,但一种有趣的可能性是它是WT1基因的反义调节因子。了解控制这些基因时空调节的事件将大大提高我们研究WT1和WIT-1在泌尿生殖系统发育中作用的能力。我们发现,虽然含有WT1基因5'区域0.6 - 2.5 kb的嵌合报告基因构建体可在许多不同细胞系中指导转录,但我们无法在13.5天的小鼠胚胎中检测到表达。然而,一个包含约42 kb该区域的黏粒能够在小鼠睾丸间质细胞(TM3)的稳定转染子或转基因胚胎中从适当的转录起始位点指导大量mRNA的表达。我们目前正在定位这种表达所需的DNA元件。