Larade K, Nimigan A, Storey K B
Institute of Biochemistry and Department of Biology, Carleton University, Ottawa, Ontario, Canada K1S 5B6.
J Exp Zool. 2001 Dec 1;290(7):759-68. doi: 10.1002/jez.1126.
Differential screening of a hepatopancreas cDNA library derived from the marine snail Littorina littorea yielded a 421-bp clone coding for ribosomal protein L26 that was up-regulated during anoxia exposure. The deduced amino acid sequence, containing 144 residues with a predicted molecular weight of 17 kDa, showed 80% amino acid sequence identity to the mammalian ribosomal protein L26. Analysis of hepatopancreas and foot muscle samples from a time course of anoxia exposure showed a maximal transcript increase of 4- and 3-fold after 96 hr and 48 hr, respectively, relative to normoxic animals, with a subsequent decrease in transcript levels during normoxic recovery. Nuclear run-off assays confirmed the observed transcriptional up-regulation of L26 during anoxia. Organ culture experiments were performed to determine a possible pathway of up-regulation of L26, with data indicating a putative role for cGMP in signal transduction. The transcriptional up-regulation of L26 during anoxia may stabilize the existing mRNA pool, via a possible cGMP-mediated signaling cascade, until oxygen reappears and protein synthesis resumes.
对来自海洋蜗牛滨螺的肝胰腺cDNA文库进行差异筛选,得到了一个编码核糖体蛋白L26的421 bp克隆,该克隆在缺氧暴露期间上调。推导的氨基酸序列含有144个残基,预测分子量为17 kDa,与哺乳动物核糖体蛋白L26的氨基酸序列同一性为80%。对缺氧暴露时间过程中的肝胰腺和足部肌肉样本分析表明,相对于常氧动物,在96小时和48小时后,转录本分别最大增加4倍和3倍,随后在常氧恢复期间转录本水平下降。核转录分析证实了缺氧期间L26转录上调。进行了器官培养实验以确定L26上调可能的途径,数据表明cGMP在信号转导中可能起作用。缺氧期间L26的转录上调可能通过可能的cGMP介导的信号级联稳定现有的mRNA库,直到氧气重新出现且蛋白质合成恢复。