Infante Carlos, Asensio Esther, Cañavate José Pedro, Manchado Manuel
IFAPA Centro El Toruño, Junta de Andalucía, Camino Tiro de pichón s/n, 11500 El Puerto de Santa María, Cádiz, Spain.
BMC Mol Biol. 2008 Jan 30;9:19. doi: 10.1186/1471-2199-9-19.
Eukaryotic elongation factor 1 alpha (eEF1A) is one of the four subunits composing eukaryotic translation elongation factor 1. It catalyzes the binding of aminoacyl-tRNA to the A-site of the ribosome in a GTP-dependent manner during protein synthesis, although it also seems to play a role in other non-translational processes. Currently, little information is still available about its expression profile and regulation during flatfish metamorphosis. With regard to this, Senegalese sole (Solea senegalensis) is a commercially important flatfish in which eEF1A gene remains to be characterized.
The development of large-scale genomics of Senegalese sole has facilitated the identification of five different eEF1A genes, referred to as SseEF1A1, SseEF1A2, SseEF1A3, SseEF1A4, and Sse42Sp50. Main characteristics and sequence identities with other fish and mammalian eEF1As are described. Phylogenetic and tissue expression analyses allowed for the identification of SseEF1A1 and SseEF1A2 as the Senegalese sole counterparts of mammalian eEF1A1 and eEF1A2, respectively, and of Sse42Sp50 as the ortholog of Xenopus laevis and teleost 42Sp50 gene. The other two elongation factors, SseEF1A3 and SseEF1A4, represent novel genes that are mainly expressed in gills and skin. The expression profile of the five genes was also studied during larval development, revealing different behaviours. To study the possible regulation of SseEF1A gene expressions by thyroid hormones (THs), larvae were exposed to the goitrogen thiourea (TU). TU-treated larvae exhibited lower SseEF1A4 mRNA levels than untreated controls at both 11 and 15 days after treatment, whereas transcripts of the other four genes remained relatively unchanged. Moreover, addition of exogenous T4 hormone to TU-treated larvae increased significantly the steady-state levels of SseEF1A4 with respect to untreated controls, demonstrating that its expression is up-regulated by THs.
We have identified five different eEF1A genes in the Senegalese sole, referred to as SseEF1A1, SseEF1A2, SseEF1A3, SseEF1A4, and Sse42Sp50. The five genes exhibit different expression patterns in tissues and during larval development. TU and T4 treatments demonstrate that SseEF1A4 is up-regulated by THs, suggesting a role in the translational regulation of the factors involved in the dramatic changes that occurs during Senegalese sole metamorphosis.
真核生物延伸因子1α(eEF1A)是构成真核生物翻译延伸因子1的四个亚基之一。在蛋白质合成过程中,它以GTP依赖的方式催化氨酰tRNA与核糖体A位点的结合,尽管它似乎也在其他非翻译过程中发挥作用。目前,关于其在比目鱼变态过程中的表达谱和调控的信息仍然很少。关于这一点,塞内加尔鳎(Solea senegalensis)是一种具有重要商业价值的比目鱼,其eEF1A基因仍有待鉴定。
塞内加尔鳎大规模基因组学的发展促进了五个不同的eEF1A基因的鉴定,分别称为SseEF1A1、SseEF1A2、SseEF1A3、SseEF1A4和Sse42Sp50。描述了它们与其他鱼类和哺乳动物eEF1A的主要特征和序列同一性。系统发育和组织表达分析分别鉴定出SseEF1A1和SseEF1A2是哺乳动物eEF1A1和eEF1A2在塞内加尔鳎中的对应物,以及Sse42Sp50是非洲爪蟾和硬骨鱼42Sp50基因的直系同源物。另外两个延伸因子SseEF1A3和SseEF1A4代表主要在鳃和皮肤中表达的新基因。还研究了这五个基因在幼体发育过程中的表达谱,揭示了不同的表达模式。为了研究甲状腺激素(THs)对SseEF1A基因表达的可能调控,将幼体暴露于致甲状腺肿物质硫脲(TU)。在处理后的第11天和第15天,TU处理的幼体的SseEF1A4 mRNA水平均低于未处理的对照,而其他四个基因的转录本相对保持不变。此外,向TU处理的幼体中添加外源性T4激素相对于未处理的对照显著增加了SseEF1A4的稳态水平,表明其表达受THs上调。
我们在塞内加尔鳎中鉴定出五个不同的eEF1A基因,分别称为SseEF1A1、SseEF1A2、SseEF1A3、SseEF1A4和Sse42Sp50。这五个基因在组织和幼体发育过程中表现出不同的表达模式。TU和T4处理表明SseEF1A4受THs上调,这表明其在塞内加尔鳎变态过程中发生的剧烈变化所涉及的因子的翻译调控中发挥作用。