Organization of the pronephric kidney revealed by large-scale gene expression mapping

被引:85
作者
Raciti, Daniela [1 ]
Reggiani, Luca [1 ]
Geffers, Lars [2 ]
Jiang, Qiuhong [2 ]
Bacchion, Francesca [1 ]
Subrizi, Astrid E. [1 ]
Clements, Dave [3 ]
Tindal, Christopher [3 ]
Davidson, Duncan R. [3 ]
Kaissling, Brigitte [4 ]
Braendli, Andre W. [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, Inst Pharmaceut Sci, CH-8093 Zurich, Switzerland
[2] Max Planck Inst Biophys Chem, Dept Genes & Behav, D-37077 Gottingen, Germany
[3] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Univ Zurich, Inst Anat, CH-8057 Zurich, Switzerland
基金
英国医学研究理事会;
关键词
D O I
10.1186/gb-2008-9-5-r84
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The pronephros, the simplest form of a vertebrate excretory organ, has recently become an important model of vertebrate kidney organogenesis. Here, we elucidated the nephron organization of the Xenopus pronephros and determined the similarities in segmentation with the metanephros, the adult kidney of mammals. Results: We performed large-scale gene expression mapping of terminal differentiation markers to identify gene expression patterns that define distinct domains of the pronephric kidney. We analyzed the expression of over 240 genes, which included members of the solute carrier, claudin, and aquaporin gene families, as well as selected ion channels. The obtained expression patterns were deposited in the searchable European Renal Genome Project Xenopus Gene Expression Database. We found that 112 genes exhibited highly regionalized expression patterns that were adequate to define the segmental organization of the pronephric nephron. Eight functionally distinct domains were discovered that shared significant analogies in gene expression with the mammalian metanephric nephron. We therefore propose a new nomenclature, which is in line with the mammalian one. The Xenopus pronephric nephron is composed of four basic domains: proximal tubule, intermediate tubule, distal tubule, and connecting tubule. Each tubule may be further subdivided into distinct segments. Finally, we also provide compelling evidence that the expression of key genes underlying inherited renal diseases in humans has been evolutionarily conserved down to the level of the pronephric kidney. Conclusion: The present study validates the Xenopus pronephros as a genuine model that may be used to elucidate the molecular basis of nephron segmentation and human renal disease.
引用
收藏
页数:21
相关论文
共 96 条
[1]   SUBTYPES OF INTERCALATED CELLS IN RAT-KIDNEY COLLECTING DUCT DEFINED BY ANTIBODIES AGAINST ERYTHROID BAND-3 AND RENAL VACUOLAR H+-ATPASE [J].
ALPER, SL ;
NATALE, J ;
GLUCK, S ;
LODISH, HF ;
BROWN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5429-5433
[2]  
[Anonymous], 2008, SELDIN GIEBISCHS KID, DOI DOI 10.1016/B978-012088488-9.50007-3
[3]   Claudins at the gate: determinants of renal epithelial tight junction paracellular permeability [J].
Balkovetz, DF .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (03) :F572-F579
[4]   SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis [J].
Bergwitz, C ;
Roslin, NM ;
Tieder, M ;
Loredo-Osti, JC ;
Bastepe, M ;
Abu-Zahra, H ;
Frappier, D ;
Burkett, K ;
Carpenter, O ;
Anderson, D ;
Garabédian, M ;
Sermet, I ;
Fujiwara, TM ;
Morgan, K ;
Tenenhouse, HS ;
Jüppner, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 78 (02) :179-192
[5]   SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance [J].
Borsani, G ;
Bassi, MT ;
Sperandeo, MP ;
De Grandi, A ;
Buoninconti, A ;
Riboni, M ;
Manzoni, M ;
Incerti, B ;
Pepe, A ;
Andria, G ;
Ballabio, A ;
Sebastio, G .
NATURE GENETICS, 1999, 21 (03) :297-301
[6]  
Brändli AW, 1999, INT J DEV BIOL, V43, P381
[7]  
BRANDLI AW, 1995, DEV DYNAM, V203, P119
[8]   CYSTINURIA CAUSED BY MUTATIONS IN RBAT, A GENE INVOLVED IN THE TRANSPORT OF CYSTINE [J].
CALONGE, MT ;
GASPARINI, P ;
CHILLARON, J ;
CHILLON, M ;
GALLUCCI, M ;
ROUSAUD, F ;
ZELANTE, L ;
TESTAR, X ;
DALLAPICCOLA, B ;
DISILVERIO, F ;
BARCELO, P ;
ESTIVILL, X ;
ZORZANO, A ;
NUNES, V ;
PALACIN, M .
NATURE GENETICS, 1994, 6 (04) :420-425
[9]   Localization of thiazide-sensitive Na+-Cl- cotransport and associated gene products in mouse DCT [J].
Câmpean, V ;
Kricke, J ;
Ellison, D ;
Luft, FC ;
Bachmann, S .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2001, 281 (06) :F1028-F1035
[10]   A crucial nephron segment in acid-base and electrolyte transport: The connecting tubule [J].
Capasso, G. .
KIDNEY INTERNATIONAL, 2006, 70 (10) :1674-1676