Cai Q, Greenway S C, Storey K B
Institute of Biochemistry and Department of Biology, Carleton University, Ottawa, Ont., Canada.
Biochim Biophys Acta. 1997 Jul 17;1353(1):69-78. doi: 10.1016/s0167-4781(97)00057-2.
The gene Aat coding for ADP/ATP translocase (AAT) was cloned from liver of the freeze-tolerant wood frog, Rana sylvatica, via differential screening of a cDNA library from liver of frozen frogs and using probes from control versus frozen frogs. Sequence analysis showed that clone pBfFR07 bearing the AAT cDNA contained a 1318-bp insert with one full-length open reading frame. The deduced amino acid sequence included 317 residues, with 81-86% identities to mammalian AAT. A 1750-nt transcript from the Aat gene was detected using pBfFR07 probe and a putative frog AAT of over 30 kDa was visualized by immunoblotting using a polyclonal antibody raised against chicken AAT. Analysis of liver samples from a time course of freezing showed a maximal 4.5-fold increase in mRNA after 8 h with AAT protein peaking in 24-h frozen frogs. Freezing also induced Aat expression in bladder and lung. In liver, mRNA expression also responded positively to anoxia stress but not to experimental dehydration of the animals. These results suggest that AAT induction during freezing may be stimulated by the ischemia that develops when plasma freezes; changes in AAT may contribute to stabilizing energetics in mitochondrial versus cytosolic pools over freeze/thaw cycles.
通过对冻存青蛙肝脏cDNA文库进行差异筛选,并使用来自对照青蛙和冻存青蛙的探针,从耐冻林蛙(Rana sylvatica)的肝脏中克隆出编码ADP/ATP转位酶(AAT)的基因Aat。序列分析表明,携带AAT cDNA的克隆pBfFR07包含一个1318 bp的插入片段,带有一个全长开放阅读框。推导的氨基酸序列包含317个残基,与哺乳动物AAT的同一性为81-86%。使用pBfFR07探针检测到来自Aat基因的1750 nt转录本,并用针对鸡AAT产生的多克隆抗体通过免疫印迹法观察到推定的分子量超过30 kDa的青蛙AAT。对冷冻过程中不同时间点的肝脏样本分析表明,8小时后mRNA最大增加4.5倍,AAT蛋白在冻存24小时的青蛙中达到峰值。冷冻还诱导膀胱和肺中Aat的表达。在肝脏中,mRNA表达对缺氧应激也有积极反应,但对动物的实验性脱水无反应。这些结果表明,冷冻过程中AAT的诱导可能受到血浆冻结时发生的局部缺血的刺激;AAT的变化可能有助于在冻融循环中稳定线粒体与细胞质池中的能量。