生物
过氧化物酶体
精子发生
融合蛋白
精母细胞
基因
分子生物学
过氧化物酶体靶向信号
细胞生物学
遗传学
重组DNA
减数分裂
内分泌学
作者
K. Kaczmarek,E. Niedzialkowska,Maja Studencka‐Turski,Y. Schulz,Paweł Grzmil
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 <i>Ccdc33</i> is predominantly expressed in the testis and undergoes alternative splicing to produce at least 4 different transcripts. The protein encoded by <i>Ccdc33</i> 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 <i>Ccdc33</i> 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.
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