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Wnt4突变小鼠肾脏的转录谱分析确定了在肾单位形成过程中表达的基因。

Transcriptional profiling of Wnt4 mutant mouse kidneys identifies genes expressed during nephron formation.

作者信息

Valerius M Todd, McMahon Andrew P

机构信息

Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.

出版信息

Gene Expr Patterns. 2008 May;8(5):297-306. doi: 10.1016/j.gep.2008.02.001. Epub 2008 Feb 9.

Abstract

The mature nephron forms from a simple epithelial vesicle into an elaborate structure with distinct regions of specialized physiological function. The molecular components driving the process of nephron development are not well understood. To identify genes that may be informative in this process we conducted a transcriptional profiling screen using Wnt4 mutant kidneys. In Wnt4-/- homozygous mice, condensates and pretubular aggregates are induced, however, epithelial renal vesicles fail to form and subsequent tubulogenesis is blocked. A transcriptional profile comparison between wildtype and Wnt4-/- mutant kidneys at E14.5 was performed using Affymetrix oligonucleotide microarrays to identify nephron-expressed genes. This approach identified 236 genes with expression levels >1.8-fold higher in wildtype versus mutant kidneys, amongst these were a number of known nephron component markers confirming the validity of the screen. These results were further detailed by wholemount in situ hybridization (WISH) of E15.5 urogenital systems (UGS). We annotated the spatial expression pattern of these genes into eight categories of expression. Genes expressed in renal vesicle and their derivatives, structures absent in the mutant, accounted for the largest number of the observed expression patterns. A number of additional genes in areas not directly overlapping the Wnt4 expression domain were also identified including the cap mesenchyme, the collecting duct, and the cortical interstitium. This study provides a useful compendium of molecular markers for the study of nephrogenesis.

摘要

成熟的肾单位从一个简单的上皮囊泡发育成一个具有独特区域且具备专门生理功能的复杂结构。驱动肾单位发育过程的分子成分尚未完全明确。为了鉴定在此过程中可能具有参考价值的基因,我们利用Wnt4突变体肾脏进行了转录谱筛选。在Wnt4基因敲除的纯合小鼠中,会诱导凝聚物和肾小管前聚集体的形成,然而,上皮性肾小囊无法形成,随后的肾小管形成过程也被阻断。利用Affymetrix寡核苷酸微阵列对E14.5期野生型和Wnt4基因敲除突变体肾脏进行转录谱比较,以鉴定肾单位表达的基因。该方法鉴定出236个在野生型肾脏中表达水平比突变体肾脏高1.8倍以上的基因,其中包括一些已知的肾单位成分标志物,证实了筛选的有效性。通过对E15.5期泌尿生殖系统(UGS)进行全胚胎原位杂交(WISH),进一步细化了这些结果。我们将这些基因的空间表达模式注释为八类表达。在肾小囊及其衍生物中表达的基因(这些结构在突变体中不存在),在观察到的表达模式中占比最大。还鉴定出了一些在与Wnt4表达域不直接重叠区域的其他基因,包括帽状间充质、集合管和皮质间质。这项研究为肾发生研究提供了一份有用的分子标志物汇编。

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