Two oligopeptide transporters from Caenorhabditis elegans:: molecular cloning and functional expression

被引:35
作者
Fei, YJ [1 ]
Fujita, T [1 ]
Lapp, DF [1 ]
Ganapathy, V [1 ]
Leibach, FH [1 ]
机构
[1] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
关键词
D O I
10.1042/bj3320565
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
Two novel oligopeptide transporter cDNA clones, CPTA and CPTB, were identified by screening a Caenorhabditis elegans cDNA library using homology hybridization. The transporter proteins deduced from the cDNAs possess multiple transmembrane domains and reveal a moderate similarity to their mammalian counterparts in amino acid sequences. CPTA and CPTB, when expressed in Xenopus laevis oocytes and studied by both radiotracer flux and microelectrode voltage-clamp protocol, displayed a saturable electrogenic transport activity driven by a proton gradient with an overlapping broad spectrum of substrate specificity. Both transporters recognize di-, tri- and tetra-peptides including phenylalanylmethionylarginylphenylalaninamide (FMRFamide) and N-acetylaspartylglutamate, members of a large neuropeptide family commonly found throughout the animal kingdom. Kinetic analysis, however, revealed that CPTA and CPTB differed in their affinity for the peptide substrates, the former being a high-affinity type and the latter a low-affinity type. CPTA and CPTB are encoded by two distinct genes localized on separate chromosomes and are expressed during the whole life span of the organism.
引用
收藏
页码:565 / 572
页数:8
相关论文
共 25 条
[1]   Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter [J].
Boll, M ;
Herget, M ;
Wagener, M ;
Weber, WM ;
Markovich, D ;
Biber, J ;
Clauss, W ;
Murer, H ;
Daniel, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :284-289
[2]   EXPRESSION CLONING OF A CDNA FROM RABBIT SMALL-INTESTINE RELATED TO PROTON-COUPLED TRANSPORT OF PEPTIDES, BETA-LACTAM ANTIBIOTICS AND ACE-INHIBITORS [J].
BOLL, M ;
MARKOVICH, D ;
WEBER, WM ;
KORTE, H ;
DANIEL, H ;
MURER, H .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1994, 429 (01) :146-149
[3]   Transport mechanism of the cloned potato H+/sucrose cotransporter StSUT1 [J].
Boorer, KJ ;
Loo, DDF ;
Frommer, WB ;
Wright, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (41) :25139-25144
[4]  
Chalfie M, 1995, Science, V270, P415
[5]  
Chalfie M., 1988, NEMATODE CAENORHABDI, P337
[6]   Identification of the histidyl residue obligatory for the catalytic activity of the human H+/peptide cotransporters PEPT1 and PEPT2 [J].
Fei, YJ ;
Liu, W ;
Prasad, PD ;
Kekuda, R ;
Oblak, TG ;
Ganapathy, V ;
Leibach, FH .
BIOCHEMISTRY, 1997, 36 (02) :452-460
[7]  
Fei YJ, 1998, PROG NUCLEIC ACID RE, V58, P239
[8]   EXPRESSION CLONING OF A MAMMALIAN PROTON-COUPLED OLIGOPEPTIDE TRANSPORTER [J].
FEI, YJ ;
KANAI, Y ;
NUSSBERGER, S ;
GANAPATHY, V ;
LEIBACH, FH ;
ROMERO, MF ;
SINGH, SK ;
BORON, WF ;
HEDIGER, MA .
NATURE, 1994, 368 (6471) :563-566
[9]  
Ganapathy V, 1996, Curr Opin Nephrol Hypertens, V5, P395, DOI 10.1097/00041552-199609000-00003
[10]  
Ganapathy Vadivel, 1994, P1773