Shetty Jagathpala, Klotz Kenneth L, Wolkowicz Michael J, Flickinger Charles J, Herr John C
Center for Research in Contraceptive and Reproductive Health, Department of Cell Biology, University of Virginia Health Sciences Center, Charlottesville, VA 22908, USA.
Gene. 2007 Jul 1;396(1):93-107. doi: 10.1016/j.gene.2007.02.031. Epub 2007 Mar 23.
To identify novel sperm alloantigens relevant to immune infertility, sera from infertile men containing antisperm antibodies (ASA) were employed on 2-D immunoblots of human sperm proteins. An immunoreactive protein spot (MW: 44 kDa, pI: 4.5) was microsequenced and the related cDNA was cloned yielding a 309 amino acid sequence corresponding to a gene currently annotated in Genbank as TSGA2 homolog (mouse) to signify 'testis specific gene A2'. In Genbank the protein deduced from this gene is currently named human meichroacidin, an orthologue of meichroacidin previously identified in mouse spermatocytes. Human TSGA2 mapped to chromosome 21q22.3. Human meichroacidin (hMCA) contained a single potential tyrosine phosphorylation site and five casein kinase phosporylation motifs. The N-terminus contained a Membrane Occupation Recognition Nexus (MORN) motif found in the lipid kinase-phosphatidylinositol 4-phosphate 5-kinase (PIP5K) family and junctophilins. However hMCA lacked the characteristic kinase homology domain of PIP5K. Northern blot analysis revealed 1.5 kb hMCA transcripts in testis and trachea with lower levels in thyroid and spinal cord. A semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) analysis demonstrated occurrence of the mRNA messages in all the ciliated tissues tested with highest levels of messages in testis and trachea. Western blot analysis showed the presence of hMCA protein in brain, thyroid and trachea at the identical mass, 44 kDa, as in human testis. However, this immunoreactive pattern differed from that of sperm in which a 38 kDa form was also evident suggesting that hMCA undergoes proteolytic processing. In human testis, hMCA localized to the tails of developing spermatids and did not localize to the nucleus of either spermatocytes or spermatids. EM immunocytochemistry localized hMCA within the radial spokes of the axonemal complex of the sperm flagellum, and immunofluorescence studies revealed h-meichroacidin in the cilia of epithelial cells in the trachea and ependyma. Bioinformatic identification of orthologues of meichroacidin in several lower organisms including ciliates and flagellates suggest the protein plays a role in flagellar motility across phyla. We propose the term radial spoke protein 44 as an accurate designation, preferable to human meichroacidin because it denotes the restricted localization of the protein to the radial spokes of the axonemes of both sperm and cilia. Further, since the human gene is expressed in brain, thyroid, trachea and lung in addition to testis, we suggest that the gene name be changed from TSGA2 [testis specific gene A2] to radial spoke protein 44 [RSP44].
为了鉴定与免疫性不育相关的新型精子同种异体抗原,将含有抗精子抗体(ASA)的不育男性血清用于人类精子蛋白的二维免疫印迹分析。对一个免疫反应性蛋白斑点(分子量:44 kDa,等电点:4.5)进行微量测序,并克隆相关的cDNA,得到一个309个氨基酸的序列,对应于Genbank中目前注释为TSGA2同源物(小鼠)的基因,以表示“睾丸特异性基因A2”。在Genbank中,从该基因推导的蛋白质目前被命名为人类美克罗酸蛋白,是先前在小鼠精母细胞中鉴定出的美克罗酸蛋白的直系同源物。人类TSGA2定位于21号染色体q22.3。人类美克罗酸蛋白(hMCA)含有一个潜在的酪氨酸磷酸化位点和五个酪蛋白激酶磷酸化基序。N端包含一个在脂质激酶 - 磷脂酰肌醇4 - 磷酸5 - 激酶(PIP5K)家族和连接膜蛋白中发现的膜占据识别连接(MORN)基序。然而,hMCA缺乏PIP5K的特征性激酶同源结构域。Northern印迹分析显示在睾丸和气管中有1.5 kb的hMCA转录本,在甲状腺和脊髓中的水平较低。半定量逆转录聚合酶链反应(RT - PCR)分析表明,在所测试的所有纤毛组织中均有mRNA信息的存在,其中在睾丸和气管中的信息水平最高。Western印迹分析表明,在脑、甲状腺和气管中存在与人类睾丸中相同质量(44 kDa)的hMCA蛋白。然而,这种免疫反应模式与精子不同,在精子中还明显存在一种38 kDa的形式,这表明hMCA经历了蛋白水解加工。在人类睾丸中,hMCA定位于发育中的精子细胞的尾部,而不定位于精母细胞或精子细胞的细胞核。电子显微镜免疫细胞化学将hMCA定位在精子鞭毛轴丝复合体的放射辐条内,免疫荧光研究揭示了气管和室管膜上皮细胞纤毛中有h - 美克罗酸蛋白。对包括纤毛虫和鞭毛虫在内的几种低等生物中美克罗酸蛋白直系同源物的生物信息学鉴定表明,该蛋白在跨门的鞭毛运动中起作用。我们提出术语“放射辐条蛋白44”作为准确的命名,比人类美克罗酸蛋白更合适,因为它表示该蛋白在精子和纤毛轴丝的放射辐条中的局限性定位。此外,由于人类基因除了在睾丸中表达外,还在脑、甲状腺、气管和肺中表达,我们建议将基因名称从TSGA2 [睾丸特异性基因A2]更改为放射辐条蛋白44 [RSP44]。