Liu Mingjuan, Reimschuessel Renate, Hassel Bret A
Molecular and Cellular Biology Program, University of Maryland-Baltimore, 108 N. Greene Street, Baltimore, MD 21201, USA.
Gene. 2002 Oct 2;298(2):129-39. doi: 10.1016/s0378-1119(02)00932-0.
In mammals, the response to nephrotoxicant-induced renal injury is limited to repair of the proximal tubule by surviving epithelial cells. In contrast, bony fish are capable of both repair, and de novo production of nephrons in response to renal damage. Importantly, toxicant-induced nephron neogenesis in goldfish (Carassius auratus) parallels nephron development in the mammalian embryo, providing a vertebrate model for kidney development. We utilized this model system to identify genes induced by the renal toxicant, gentamicin, that may function in nephron neogenesis. A novel ubiquitin-like (UBL) gene, 40.1, was identified by differential display analysis of control and gentamicin-treated goldfish kidney. 40.1 was induced dramatically 3-7 days following a sublethal dose of gentamicin, and returned to basal level by 14 days post-treatment. The induction of 40.1 coincided with early renal injury in the proximal tubules of gentamicin-injected fish; however, expression was not restricted to the kidney, suggesting that 40.1 induction may be a more general response to cell injury. Sequence analysis revealed that 40.1 contains tandem UBL domains, and shares homology with ISG15, a 15 kD interferon-(IFN) stimulated UBL found in mammals. Analysis of the genome database for the pufferfish, Fugu rubrides, identified a goldfish ISG15 (gfISG15) homologue with an IFN-stimulated response element in the promoter region, providing further evidence that gfISG15 is the true teleost ISG15 orthologue. Zebrafish and catfish ISG15 genes were subsequently identified by sequence analysis. Consistent with its predicted function as a UBL, gfISG15 formed conjugates with cellular proteins in vitro and in transient transfections. Similar to the induction of mammalian ISG15 by microbial challenge, gfISG15 was induced in the spleen of mycobacteria-infected fish. These studies identified the first teleost ISG15 orthologue. The induction of gfISG15 as an early genetic event in response to a renal toxicant, and its conserved, stress-associated, expression in higher vertebrates suggests that ISG15 is an important component of the host response to diverse stress stimuli.
在哺乳动物中,对肾毒性物质诱导的肾损伤的反应仅限于存活的上皮细胞对近端小管的修复。相比之下,硬骨鱼不仅能够修复,还能在肾损伤时重新生成肾单位。重要的是,金鱼(Carassius auratus)中由毒物诱导的肾单位新生与哺乳动物胚胎中的肾单位发育相似,为肾脏发育提供了一个脊椎动物模型。我们利用这个模型系统来鉴定由肾毒性物质庆大霉素诱导的、可能在肾单位新生中起作用的基因。通过对对照和庆大霉素处理的金鱼肾脏进行差异显示分析,鉴定出一个新的类泛素(UBL)基因40.1。在亚致死剂量的庆大霉素处理后3 - 7天,40.1显著诱导表达,并在处理后14天恢复到基础水平。40.1的诱导与注射庆大霉素的鱼近端小管的早期肾损伤同时发生;然而,其表达并不局限于肾脏,这表明40.1的诱导可能是对细胞损伤更普遍的反应。序列分析显示40.1含有串联的UBL结构域,并且与ISG15同源,ISG15是在哺乳动物中发现的一种受15 kD干扰素(IFN)刺激的UBL。对河豚Fugu rubrides的基因组数据库分析发现,金鱼ISG15(gfISG15)同源物的启动子区域有一个干扰素刺激反应元件,这进一步证明gfISG15是真正的硬骨鱼ISG15直系同源物。随后通过序列分析鉴定出斑马鱼和鲶鱼的ISG15基因。与其作为UBL的预测功能一致,gfISG15在体外和瞬时转染中与细胞蛋白形成缀合物。与微生物刺激诱导哺乳动物ISG15相似,gfISG15在感染分枝杆菌的鱼的脾脏中被诱导。这些研究鉴定出了首个硬骨鱼ISG15直系同源物。gfISG15作为对肾毒性物质反应的早期遗传事件的诱导,以及其在高等脊椎动物中保守的、与应激相关的表达,表明ISG15是宿主对多种应激刺激反应的重要组成部分。