Department of Biological Sciences, Lehigh University, Bethlehem, PA, USA.
Nucleus. 2013 May-Jun;4(3):241-58. doi: 10.4161/nucl.25261. Epub 2013 Jun 6.
Duplicated ribosomal protein (Rp) gene families often encode highly similar or identical proteins with redundant or unique roles. Eukaryotic-specific paralogues RpL22e and RpL22e-like-PA are structurally divergent within the N terminus and differentially expressed, suggesting tissue-specific functions. We previously identified RpL22e-like-PA as a testis Rp. Strikingly, RpL22e is detected in immunoblots at its expected molecular mass (m) of 33 kD and at increasing m of ~43-55 kD, suggesting RpL22e post-translational modification (PTM). Numerous PTMs, including N-terminal SUMOylation, are predicted computationally. Based on S2 cell co-immunoprecipitations, bacterial-based SUMOylation assays and in vivo germline-specific RNAi depletion of SUMO, we conclude that RpL22e is a SUMO substrate. Testis-specific PTMs are evident, including a phosphorylated version of SUMOylated RpL22e identified by in vitro phosphatase experiments. In ribosomal profiles from S2 cells, only unconjugated RpL22e co-sediments with active ribosomes, supporting an extra-translational role for SUMOylated RpL22e. Ectopic expression of an RpL22e N-terminal deletion (lacking SUMO motifs) shows that truncated RpL22e co-sediments with polysomes, implying that RpL22e SUMOylation is dispensable for ribosome biogenesis and function. In mitotic germ cells, both paralogues localize within the cytoplasm and nucleolus. However, within meiotic cells, phase contrast microscopy and co-immunohistochemical analysis with nucleolar markers nucleostemin1 and fibrillarin reveals diffuse nucleoplasmic, but not nucleolar RpL22e localization that transitions to a punctate pattern as meiotic cells mature, suggesting an RpL22e role outside of translation. Germline-specific knockdown of SUMO shows that RpL22e nucleoplasmic distribution is sensitive to SUMO levels, as immunostaining becomes more dispersed. Overall, these data suggest distinct male germline roles for RpL22e and RpL22e-like-PA.
核糖体蛋白 (Rp) 基因家族的重复通常编码具有冗余或独特作用的高度相似或相同的蛋白质。真核生物特异性的 paralogues RpL22e 和 RpL22e-like-PA 在 N 端结构上有差异,表达不同,提示具有组织特异性功能。我们之前发现 RpL22e-like-PA 是一种睾丸 Rp。引人注目的是,RpL22e 在免疫印迹中以其预期的分子量 (m) 33 kD 检测到,并以 ~43-55 kD 的递增 m 检测到,提示 RpL22e 翻译后修饰 (PTM)。计算预测存在许多 PTM,包括 N 端 SUMOylation。基于 S2 细胞的共免疫沉淀、基于细菌的 SUMOylation 测定和体内生殖细胞特异性 SUMO 的 RNAi 耗竭,我们得出结论,RpL22e 是 SUMO 的底物。在睾丸中存在特异性的 PTM,包括通过体外磷酸酶实验鉴定的 SUMOylated RpL22e 的磷酸化版本。在 S2 细胞的核糖体图谱中,只有未缀合的 RpL22e 与活性核糖体共沉降,支持 SUMOylated RpL22e 的翻译后作用。RpL22e N 端缺失 (缺乏 SUMO 基序) 的异位表达表明截断的 RpL22e 与多核糖体共沉降,这意味着 RpL22e SUMOylation对于核糖体的生物发生和功能不是必需的。在有丝分裂生殖细胞中,两个 paralogues 都定位于细胞质和核仁内。然而,在减数分裂细胞中,相差显微镜观察和与核仁标记物 nucleostemin1 和 fibrillarin 的共免疫组织化学分析显示,弥漫性核质,但不是核仁 RpL22e 定位在减数分裂细胞成熟时转变为点状模式,提示 RpL22e 在翻译之外具有作用。生殖细胞特异性 SUMO 敲低表明 RpL22e 核质分布对 SUMO 水平敏感,免疫染色变得更加分散。总的来说,这些数据表明 RpL22e 和 RpL22e-like-PA 在雄性生殖细胞中具有不同的作用。