Elkis Yoav, Bel Shai, Rahimi Roni, Lerer-Goldstein Tali, Levin-Zaidman Smadar, Babushkin Tatiana, Shpungin Sally, Nir Uri
The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, 52900, Israel.
Electron Microscopy Unit, Weizmann Institute of Science, Rehovot, 7610001, Israel.
PLoS One. 2015 Dec 23;10(12):e0145277. doi: 10.1371/journal.pone.0145277. eCollection 2015.
TMF/ARA160 is known to be a TATA element Modulatory Factor (TMF). It was initially identified as a DNA-binding factor and a coactivator of the Androgen receptor. It was also characterized as a Golgi-associated protein, which is essential for acrosome formation during functional sperm development. However, the molecular roles of TMF in this intricate process have not been revealed. Here, we show that during spermiogenesis, TMF undergoes a dynamic change of localization throughout the Golgi apparatus. Specifically, TMF translocates from the cis-Golgi to the trans-Golgi network and to the emerging vesicles surface, as the round spermatids develop. Notably, lack of TMF led to an abnormal spatial orientation of the Golgi and to the deviation of the trans-Golgi surface away from the nucleus of the developing round spermatids. Concomitantly, pro-acrosomal vesicles derived from the TMF-/- Golgi lacked targeting properties and did not tether to the spermatid nuclear membrane thereby failing to form the acrosome anchoring scaffold, the acroplaxome, around the cell-nucleus. Absence of TMF also perturbed the positioning of microtubules, which normally lie in proximity to the Golgi and are important for maintaining Golgi spatial orientation and dynamics and for chromatoid body formation, which is impaired in TMF-/- spermatids. In-silico evaluation combined with molecular and electron microscopic analyses revealed the presence of a microtubule interacting domain (MIT) in TMF, and confirmed the association of TMF with microtubules in spermatogenic cells. Furthermore, the MIT domain in TMF, along with microtubules integrity, are required for stable association of TMF with the Golgi apparatus. Collectively, we show here for the first time that a Golgi and microtubules associated protein is crucial for maintaining proper Golgi orientation during a cell developmental process.
已知TMF/ARA160是一种TATA元件调节因子(TMF)。它最初被鉴定为一种DNA结合因子和雄激素受体的共激活因子。它还被表征为一种与高尔基体相关的蛋白质,这对于功能性精子发育过程中的顶体形成至关重要。然而,TMF在这一复杂过程中的分子作用尚未揭示。在这里,我们表明在精子发生过程中,TMF在整个高尔基体中经历定位的动态变化。具体而言,随着圆形精子细胞的发育,TMF从顺面高尔基体转移到反面高尔基体网络以及新出现的囊泡表面。值得注意的是,缺乏TMF会导致高尔基体的空间取向异常,并导致反面高尔基体表面偏离发育中的圆形精子细胞的细胞核。同时,源自TMF基因敲除小鼠高尔基体的前顶体囊泡缺乏靶向特性,并且不与精子细胞核膜相连,从而无法在细胞核周围形成顶体锚定支架——顶体板。缺乏TMF还扰乱了微管的定位,微管通常位于高尔基体附近,对于维持高尔基体的空间取向和动态以及对于类染色质体的形成很重要,而在TMF基因敲除的精子细胞中类染色质体形成受损。计算机模拟评估结合分子和电子显微镜分析揭示了TMF中存在一个微管相互作用结构域(MIT),并证实了TMF与生精细胞中的微管相关。此外,TMF中的MIT结构域以及微管的完整性是TMF与高尔基体稳定结合所必需的。总体而言,我们首次在此表明一种与高尔基体和微管相关的蛋白质对于在细胞发育过程中维持正确的高尔基体取向至关重要。