Kaczmarek K, Niedzialkowska E, Studencka M, Schulz Y, Grzmil P
Institute of Human Genetics, University of Göttingen, Göttingen, Germany.
Cytogenet Genome Res. 2009;126(3):243-52. doi: 10.1159/000251961. Epub 2010 Jan 6.
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.
许多对雄性生育至关重要的基因通常主要或仅在雄性生殖细胞中表达。对小鼠模型的分析已证明过氧化物酶体在精子发生中的功能重要性。据报道,CCDC33蛋白是一种癌/睾丸(CT)抗原。我们发现小鼠Ccdc33主要在睾丸中表达,并经历可变剪接以产生至少4种不同的转录本。Ccdc33编码的蛋白质包含3个卷曲螺旋结构域、1个C2结构域、2个内质网(ER)膜滞留信号样基序和2个假定的2型过氧化物酶体靶向信号(PTS2)。我们能够证明第二个PTS2序列具有功能,并负责将CCDC33靶向到过氧化物酶体。此外,在HeLa细胞中,CCDC33-dsRED融合蛋白与一种已知的过氧化物酶体蛋白PXT1共定位,并显示出点状的细胞内分布。综上所述,小鼠Ccdc33编码一种假定的过氧化物酶体蛋白,主要在雄性生殖细胞中表达。其表达始于初级精母细胞阶段,表明该蛋白在精子发生过程中具有重要作用。