Kelly Shannan, Yamamoto Hideki, Robles Laura J
Department of Biology, California State University, Dominguez Hills, Carson, CA 90747, USA.
Mol Vis. 2008 Aug 4;14:1446-55.
We previously reported the differential expression and translation of mRNA and protein in dark- and light-adapted octopus retinas, which may result from cytoplasmic polyadenylation element (CPE)-dependent mRNA masking and unmasking. Here we investigate the presence of CPEs in alpha-tubulin and S-crystallin mRNA and report the identification of cytoplasmic polyadenylation element binding protein (CPEB) in light- and dark-adapted octopus retinas.
3'-RACE and sequencing were used to isolate and analyze the 3'-UTRs of alpha-tubulin and S-crystallin mRNA. Total retinal protein isolated from light- and dark-adapted octopus retinas was subjected to western blot analysis followed by CPEB antibody detection, PEP-171 inhibition of CPEB, and dephosphorylation of CPEB.
The following CPE-like sequence was detected in the 3'-UTR of isolated long S-crystallin mRNA variants: UUUAACA. No CPE or CPE-like sequences were detected in the 3'-UTRs of alpha-tubulin mRNA or of the short S-crystallin mRNA variants. Western blot analysis detected CPEB as two putative bands migrating between 60-80 kDa, while a third band migrated below 30 kDa in dark- and light-adapted retinas.
The detection of CPEB and the identification of the putative CPE-like sequences in the S-crystallin 3'-UTR suggest that CPEB may be involved in the activation of masked S-crystallin mRNA, but not in the regulation of alpha-tubulin mRNA, resulting in increased S-crystallin protein synthesis in dark-adapted octopus retinas.
我们之前报道了在暗适应和明适应的章鱼视网膜中mRNA和蛋白质的差异表达与翻译,这可能是由细胞质聚腺苷酸化元件(CPE)依赖的mRNA掩盖和去掩盖所致。在此,我们研究α-微管蛋白和S-晶体蛋白mRNA中CPE的存在情况,并报告在暗适应和明适应的章鱼视网膜中细胞质聚腺苷酸化元件结合蛋白(CPEB)的鉴定结果。
采用3'-RACE和测序技术分离并分析α-微管蛋白和S-晶体蛋白mRNA的3'-UTR。从暗适应和明适应的章鱼视网膜中分离出的总视网膜蛋白进行蛋白质免疫印迹分析,随后进行CPEB抗体检测、CPEB的PEP-171抑制以及CPEB的去磷酸化。
在分离出的长S-晶体蛋白mRNA变体的3'-UTR中检测到以下类似CPE的序列:UUUAACA。在α-微管蛋白mRNA或短S-晶体蛋白mRNA变体的3'-UTR中未检测到CPE或类似CPE的序列。蛋白质免疫印迹分析检测到CPEB为两条假定条带,迁移在60 - 80 kDa之间,而在暗适应和明适应的视网膜中第三条带迁移在30 kDa以下。
CPEB的检测以及在S-晶体蛋白3'-UTR中假定的类似CPE序列的鉴定表明,CPEB可能参与了被掩盖的S-晶体蛋白mRNA的激活,但不参与α-微管蛋白mRNA的调节,从而导致暗适应的章鱼视网膜中S-晶体蛋白的蛋白质合成增加。