Ccdc33, a Predominantly Testis-Expressed Gene, Encodes a Putative Peroxisomal Protein

被引:18
作者
Kaczmarek, K. [1 ]
Niedzialkowska, E. [1 ]
Studencka, M. [1 ]
Schulz, Y. [1 ]
Grzmil, P. [1 ,2 ]
机构
[1] Univ Gottingen, Inst Human Genet, DE-37073 Gottingen, Germany
[2] Jagiellonian Univ, Inst Zool, Dept Genet & Evolut, PL-30060 Krakow, Poland
关键词
Coiled-coil domain; Peroxisomal proteins; Peroxisomal targeting signal; Spermatogenesis; RHIZOMELIC CHONDRODYSPLASIA PUNCTATA; MALE GERM-CELLS; ADRENOLEUKODYSTROPHY GENE; TARGETED DISRUPTION; UNEXPECTED HOMOLOGY; HUMAN PEX7; DIFFERENTIATION; IDENTIFICATION; TRANSCRIPTION; HOMEOSTASIS;
D O I
10.1159/000251961
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many genes crucial for male fertility are often predominantly or exclusively expressed in male germ cells. The analysis of mouse models has demonstrated the functional importance of peroxisomes in spermatogenesis. The CCDC33 protein has been reported to be a cancer/testis (CT) antigen. We found that mouse Ccdc33 is predominantly expressed in the testis and undergoes alternative splicing to produce at least 4 different transcripts. The protein encoded by Ccdc33 contains 3 coiled-coil domains, a C2-domain, 2 ER membrane retention signal-like motifs and 2 putative peroxisomal targeting signals type 2 (PTS2). We could demonstrate that the second PTS2 sequence is functional and responsible for the targeting of CCDC33 to peroxisomes. Moreover, in HeLa cells CCDC33-dsRED fusion protein co-localized with a known peroxisomal protein, namely PXT1, and showed punctuate intracellular distribution. Taken together, the mouse Ccdc33 encodes a putative peroxisomal protein and is predominantly expressed in male germ cells. The expression starts at the primary spermatocyte stage, suggesting an important role of this protein during spermatogenesis. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:243 / 252
页数:10
相关论文
共 60 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   CHARACTERIZATION OF SEVERAL CLONAL LINES OF CULTURED LEYDIG TUMOR-CELLS - GONADOTROPIN RECEPTORS AND STEROIDOGENIC RESPONSES [J].
ASCOLI, M .
ENDOCRINOLOGY, 1981, 108 (01) :88-95
[3]   ADRENOLEUKODYSTROPHY GENE - UNEXPECTED HOMOLOGY TO A PROTEIN INVOLVED IN PEROXISOME BIOGENESIS [J].
AUBOURG, P ;
MOSSER, J ;
DOUAR, AM ;
SARDE, CO ;
LOPEZ, J ;
MANDEL, JL .
BIOCHIMIE, 1993, 75 (3-4) :293-302
[4]   Inactivation of the peroxisomal multifunctional protein-2 in mice impedes the degradation of not only 2-methyl-branched fatty acids and bile acid intermediates but also of very long chain fatty acids [J].
Baes, M ;
Huyghe, S ;
Carmeliet, P ;
Declercq, PE ;
Collen, D ;
Mannaerts, GP ;
Van Veldhoven, PP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :16329-16336
[5]   Detection of mRNAs encoding peroxisomal proteins by non-radioactive in situ hybridization with digoxigenin-labelled cRNAs [J].
Baumgart, E ;
Schad, A ;
Volkl, A ;
Fahimi, HD .
HISTOCHEMISTRY AND CELL BIOLOGY, 1997, 108 (4-5) :371-379
[6]   Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata [J].
Braverman, N ;
Steel, G ;
Obie, C ;
Moser, A ;
Moser, H ;
Gould, SJ ;
Valle, D .
NATURE GENETICS, 1997, 15 (04) :369-376
[7]   Testicular dysfunction in adrenomyeloneuropathy [J].
Brennemann, W ;
Kohler, W ;
Zierz, S ;
Klingmuller, D .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1997, 137 (01) :34-39
[8]   Impaired neuronal migration and endochondral ossification in Pex7 knockout mice:: a model for rhizomelic chondrodysplasia punctata [J].
Brites, P ;
Motley, AM ;
Gressens, P ;
Mooyer, PAW ;
Ploegaert, I ;
Everts, V ;
Evrard, P ;
Carmeliet, P ;
Dewerchin, M ;
Schoonjans, L ;
Duran, M ;
Waterham, HR ;
Wanders, RJA ;
Baes, M .
HUMAN MOLECULAR GENETICS, 2003, 12 (18) :2255-2267
[9]   Plasmalogens participate in very-long-chain fatty acid-induced pathology [J].
Brites, Pedro ;
Mooyer, Petra A. W. ;
el Mrabet, Leila ;
Waterham, Hans R. ;
Wanders, Ronald J. A. .
BRAIN, 2009, 132 :482-492
[10]   Identification of cancer/testis-antigen genes by massively parallel signature sequencing [J].
Chen, YT ;
Scanlan, MJ ;
Venditti, CA ;
Chua, R ;
Theiler, G ;
Stevenson, BJ ;
Iseli, C ;
Gure, AO ;
Vasicek, T ;
Strausberg, RL ;
Jongeneel, CV ;
Old, LJ ;
Simpson, AJG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (22) :7940-7945