Placental cathepsin M is alternatively spliced and exclusively expressed in the spongiotrophoblast layer

被引:9
作者
Bode, S [1 ]
Peters, C [1 ]
Deussing, JM [1 ]
机构
[1] Univ Freiburg, Inst Mol Med & Zellforsch, D-79104 Freiburg, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2005年 / 1731卷 / 03期
关键词
cysteine peptidase; alternative splicing; spongiotrophoblast; mouse placenta;
D O I
10.1016/j.bbaexp.2005.10.005
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
Cathepsin M and cathepsin-3 are cysteine pepticlases expressed exclusively in the murine placenta. Their expression increases continuously from 11.5 dpc until the end of gestation. The cathepsin M gene consists of 8 exons and 7 introns covering 6 kb of genomic DNA on mouse chromosome 13. Multiple variants of CTSM were identified which display alternative splicing of exon 2 or exon 7. Alternative splicing of exon 2 does not affect the translated region of CTSM whereas aberrant splicing of exon 7 wilt results in enzymatically inactive versions of CTSM which still might retain inhibitory activity towards cysteine peptidases. Besides two defined major transcription start sites the putative promoter region comprises of a TATA-box and a relatively low (41%) G+C content reflecting its highly specific spatial and temporal expression pattern. Similar features are found within the promoter region of CTS3 which is highly homologous to CTSM. Both cathepsin M and -3 expression are confined to the spongiotrophoblast layer of the mouse placenta an expression pattern which is unique among cysteine peptidases located within the cluster of cathepsin J-1ike peptidases on mouse chromosome 13. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 167
页数:8
相关论文
共 39 条
[1]  
Afonso S, 1997, DEVELOPMENT, V124, P3415
[2]  
Alexander CM, 1996, DEVELOPMENT, V122, P1723
[3]   Identification and characterization of a novel human cathepsin L splice variant [J].
Arora, S ;
Chauhan, SS .
GENE, 2002, 293 (1-2) :123-131
[4]   IDENTIFICATION OF 2 NEW EXONS AND MULTIPLE TRANSCRIPTION START POINTS IN THE 5'-UNTRANSLATED REGION OF THE HUMAN CATHEPSIN-B-ENCODING GENE [J].
BERQUIN, IM ;
CAO, LQ ;
FONG, D ;
SLOANE, BF .
GENE, 1995, 159 (02) :143-149
[5]   NONMETHYLATED CPG-RICH ISLANDS AT THE HUMAN ALPHA-GLOBIN LOCUS - IMPLICATIONS FOR EVOLUTION OF THE ALPHA-GLOBIN PSEUDOGENE [J].
BIRD, AP ;
TAGGART, MH ;
NICHOLLS, RD ;
HIGGS, DR .
EMBO JOURNAL, 1987, 6 (04) :999-1004
[6]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[7]   A NOVEL REGULATORY REGION IS REQUIRED FOR TROPHOBLAST-SPECIFIC TRANSCRIPTION IN TRANSGENIC MICE [J].
CALZONETTI, T ;
STEVENSON, L ;
ROSSANT, J .
DEVELOPMENTAL BIOLOGY, 1995, 171 (02) :615-626
[8]   Structure of human procathepsin L reveals the molecular basis of inhibition by the prosegment [J].
Coulombe, R ;
Grochulski, P ;
Sivaraman, J ;
Menard, R ;
Mort, JS ;
Cygler, M .
EMBO JOURNAL, 1996, 15 (20) :5492-5503
[9]   Genetic insights into trophoblast differentiation and placental morphogenesis [J].
Cross, JC .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2000, 11 (02) :105-113
[10]   Structure of rat procathepsin B: Model for inhibition of cysteine protease activity by the proregion [J].
Cygler, M ;
Sivaraman, J ;
Grochulski, P ;
Coulombe, R ;
Storer, AC ;
Mort, JS .
STRUCTURE, 1996, 4 (04) :405-416