Neprilysin II: A putative novel metalloprotease and its isoforms in CNS and testis

被引:51
作者
Tanja, O [1 ]
Facchinetti, P [1 ]
Rose, C [1 ]
Bonhomme, MC [1 ]
Gros, C [1 ]
Schwartz, JC [1 ]
机构
[1] INSERM, Unite 109, Unite Neurobiol & Pharmacol Mol, Ctr Paul Broca, F-75014 Paris, France
关键词
cloning; metalloprotease; neprilysin; NEP; NEPII; endothelin-converting enzyme; peptide metabolism;
D O I
10.1006/bbrc.2000.2664
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
Metalloproteases of the M13 subfamily, comprising namely neprylisin (NEP) and endothelin-converting enzyme (ECE), are involved in the metabolism of various neuronal and hormonal peptides, and inhibitors thereof have already Zed to therapeutically useful agents. Using homology cloning, we have identified a new member of this family in rat tissues. It is a glycosylated, type II integral membrane protein of 774 amino acids, containing a zinc-binding consensus motif, highly homologous to NEP and, therefore, designated NEPII. We have characterized multiple splice variants of NEPII mRNA with distinct expression patterns in brain regions, pituitary and testis. In situ hybridization of testis, where levels of the NEPII gene transcript are the highest, reveals a localization within round spermatids. In brain, NEPII is expressed heterogeneously among several neuronal populations and according to a pattern grossly complementary to that of NEP. (C) 2000 Academic Press.
引用
收藏
页码:565 / 570
页数:6
相关论文
共 25 条
[1]  
BARRETT AJ, 2004, HDB PROTEOLYTIC ENZY
[2]   EFFECTS OF ACETORPHAN, AN ENKEPHALINASE INHIBITOR, ON EXPERIMENTAL AND ACUTE DIARRHEA [J].
BAUMER, P ;
DORVAL, ED ;
BERTRAND, J ;
VETEL, JM ;
SCHWARTZ, JC ;
LECOMTE, JM .
GUT, 1992, 33 (06) :753-758
[3]   cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone [J].
Du, L ;
Desbarats, M ;
Viel, J ;
Glorieux, FH ;
Cawthorn, C ;
Ecarot, B .
GENOMICS, 1996, 36 (01) :22-28
[4]   ENDOTHELIN-CONVERTING ENZYME-2 IS A MEMBRANE-BOUND, PHOSPHORAMIDON-SENSITIVE METALLOPROTEASE WITH ACIDIC PH OPTIMUM [J].
EMOTO, N ;
YANAGISAWA, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) :15262-15268
[5]  
FACCHINETTI P, UNPUB GENE DISTRIBUT
[6]   Molecular identification and characterization of novel membrane-bound metalloprotease, the soluble secreted form of which hydrolyzes a variety of vasoactive peptides [J].
Ikeda, K ;
Emoto, N ;
Raharjo, SB ;
Nurhantari, Y ;
Saiki, K ;
Yokoyama, M ;
Matsuo, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32469-32477
[7]   Interpreting cDNA sequences: Some insights from studies on translation [J].
Kozak, M .
MAMMALIAN GENOME, 1996, 7 (08) :563-574
[8]   ROLE OF GLYCOSYLATION IN TRANSPORT AND ENZYMATIC-ACTIVITY OF NEUTRAL ENDOPEPTIDASE-24.11 [J].
LAFRANCE, MH ;
VEZINA, C ;
WANG, Q ;
BOILEAU, G ;
CRINE, P ;
LEMAY, G .
BIOCHEMICAL JOURNAL, 1994, 302 :451-454
[9]   MOLECULAR-CLONING AND PRIMARY STRUCTURE OF KELL BLOOD-GROUP PROTEIN [J].
LEE, S ;
ZAMBAS, ED ;
MARSH, WL ;
REDMAN, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6353-6357
[10]   TISSUE-SPECIFIC EXPRESSION OF RAT NEUTRAL ENDOPEPTIDASE (NEPRILYSIN) MESSENGER-RNAS [J].
LI, CW ;
BOOZE, RM ;
HERSH, LB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5723-5728