A panoramic view of gene expression in the human kidney

被引:138
作者
Chabardès-Garonne, D
Méjean, A
Aude, JC
Cheval, L
Di Stefano, A
Gaillard, MC
Imbert-Teboul, M
Wittner, M
Balian, C
Anthouard, V
Roberts, C
Ségurens, B
Wincker, P
Weissenbach, J
Doucet, A
Elalouf, JM [1 ]
机构
[1] CEA Saclay, Dept Biol Joliot Curie, Serv Biochim & Genet Mol, F-91191 Gif Sur Yvette, France
[2] CEA Saclay, CNRS, Unite Rech Associee 1859, F-91191 Gif Sur Yvette, France
[3] Hop Necker Enfants Malad, Serv Urol, F-75015 Paris, France
[4] CNS, F-91006 Evry, France
关键词
D O I
10.1073/pnas.2234604100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To gain a molecular understanding of kidney functions, we established a high-resolution map of gene expression patterns in the human kidney. The glomerulus and seven different nephron segments were isolated by microdissection from fresh tissue specimens, and their transcriptome was characterized by using the serial analysis of gene expression (SAGE) method. More than 400,000 mRNA SAGE tags were sequenced, making it possible to detect in each structure transcripts present at 18 copies per cell with a 95% confidence level. Expression of genes responsible for nephron transport and permeability properties was evidenced through transcripts for 119 solute carriers, 84 channels, 43 ion-transport ATPases, and 12 claudins. Searching for differences between the transcriptomes, we found 998 transcripts greatly varying in abundance from one nephron portion to another. Clustering analysis of these transcripts evidenced different extents of similarity between the nephron portions. Approximately 75% of the differentially distributed transcripts corresponded to cDNAs of known or unknown function that are accurately mapped in the human genome. This systematic large-scale analysis of individual structures of a complex human tissue reveals sets of genes underlying the function of well-defined nephron portions. It also provides quantitative expression data for a variety of genes mutated in hereditary diseases and helps in sorting candidate genes for renal diseases that affect specific portions of the human nephron.
引用
收藏
页码:13710 / 13715
页数:6
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