Schwarz Thomas, Prieler Barbara, Schmid Johannes A, Grzmil Pawel, Neesen Juergen
Institute for Medical Genetics, Medical University of Vienna, 1090, Vienna, Austria.
Institute for Medical Genetics, Medical University of Vienna, 1090, Vienna, Austria.
Eur J Cell Biol. 2017 May;96(3):276-288. doi: 10.1016/j.ejcb.2017.02.003. Epub 2017 Feb 20.
Disruption of murine Hook1 results in a disturbed spermatogenesis and consequently leads to male infertility in mice. Within these mice abnormal sperm development starts with a disorganization of the microtubular manchette in elongating spermatids that leads to an abnormal head shape as well as to distinctive structural changes in the flagella of the sperm. To elucidate Hook1 function in male germ cell differentiation a yeast two-hybrid screen was performed using a murine testicular library, which leads to the identification of several putative Hook1 interacting proteins. One of the isolated cDNA fragments encodes for the coiled-coil domain containing protein 181 (Ccdc181). The putative interaction of Ccdc181 with Hook1 was verified by FRET analysis and interacting regions were identified using yeast two-hybrid assays. Furthermore, Ccdc181 seems to interact directly with microtubules and localizes to the microtubular manchette of elongating spermatids, resembling the previously reported localization of Hook1. According to the observed immunostaining pattern the RNA expression of Ccdc181 is less prominent in pre-meiotic stages of sperm development but increases in the haploid phase of spermatogenesis and seems to be restricted to male germ cells. However, Ccdc181 expression is also observed to a lower extent in somatic tissues, particularly, in tissues containing ciliated epithelia. Additionally, Ccdc181 protein is found to localize to the sperm flagella and to the basal half of motile cilia, whereas Ccdc181 was not detected in primary non-motile cilia. Furthermore, we showed that Ccdc181 is a putative interacting partner of the different catalytic subunits of Pp1, raising the hypothesis that Ccdc181 plays a role in mediating ciliary motility.
破坏小鼠的Hook1会导致精子发生紊乱,进而导致小鼠雄性不育。在这些小鼠中,异常的精子发育始于伸长的精子细胞中微管袖套的紊乱,这会导致头部形状异常以及精子鞭毛出现明显的结构变化。为了阐明Hook1在雄性生殖细胞分化中的功能,利用小鼠睾丸文库进行了酵母双杂交筛选,从而鉴定出几种假定的与Hook1相互作用的蛋白质。其中一个分离的cDNA片段编码卷曲螺旋结构域包含蛋白181(Ccdc181)。通过荧光共振能量转移(FRET)分析验证了Ccdc181与Hook1的假定相互作用,并利用酵母双杂交试验确定了相互作用区域。此外,Ccdc181似乎直接与微管相互作用,并定位于伸长的精子细胞的微管袖套,类似于先前报道的Hook1的定位。根据观察到的免疫染色模式,Ccdc181的RNA表达在精子发育的减数分裂前期阶段不太明显,但在精子发生的单倍体阶段增加,并且似乎仅限于雄性生殖细胞。然而,在体细胞组织中也观察到较低水平的Ccdc181表达,特别是在含有纤毛上皮的组织中。此外,发现Ccdc181蛋白定位于精子鞭毛和运动纤毛的基部一半,而在初级非运动纤毛中未检测到Ccdc181。此外,我们表明Ccdc181是蛋白磷酸酶1(Pp1)不同催化亚基的假定相互作用伙伴,这就提出了一个假说,即Ccdc181在介导纤毛运动中起作用。