Molecular characterization of a new urea transporter in the human kidney

被引:95
作者
Olives, B
Martial, S
Mattei, MG
Matassi, G
Rousselet, G
Ripoche, P
Cartron, JP
Bailly, P
机构
[1] INST NATL TRANSFUS SANGUINE,GIP,INSERM U76,F-75015 PARIS,FRANCE
[2] CEA SACLAY,SERV BIOL CELLULAIRE,F-91191 GIF SUR YVETTE,FRANCE
[3] CHU TIMONE,INSERM U242,F-13385 MARSEILLE,FRANCE
关键词
urea transport; human kidney; tissue expression; transcription-translation assay; in situ hybridization;
D O I
10.1016/0014-5793(96)00425-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A cDNA clone (HUT2) sharing 61.1% and 89.9% sequence identity with the human erythroid (HUT11) and the rabbit (UT2) urea transporters, respectively, was isolated by homology cloning from a human kidney library, HUT2 transcripts were restricted to the kidney and the HUT2 polypeptide was not immunoprecipitated with blood group Kidd-related antibodies (anti-Jk3) in coupled transcription-translation assays, Functional expression studies in Xenopus oocytes demonstrated that HUT2-mediated urea transport was not inhibited by p-chloromercuribenzene sulfonate (pCMBS) which, however, inhibited the urea flux mediated by HUT11. These findings demonstrate that at least two distinct urea transporters are present in human tissues, By in situ hybridization, the gene encoding HUT2 has been assigned to chromosome 18q12.1-q21-1, as found previously for the Kidd/urea transporter HUT11, suggesting that both genes evolved from duplication of a common ancestor.
引用
收藏
页码:156 / 160
页数:5
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