Cai Q, Storey K B
Institute of Biochemistry, Carleton University, Ottawa, Ontario, Canada.
Am J Physiol. 1997 May;272(5 Pt 2):R1480-92. doi: 10.1152/ajpregu.1997.272.5.R1480.
Differential screening of a cDNA library produced from liver of the freeze-tolerant wood frog, Rana sylvatica, was used to search for freezing-induced genes. Five freezing-responsive cDNA clones representing different genes were isolated when approximately 80,000 plaques of a cDNA library, prepared from liver of frozen frogs (24 h at -2.5 degrees C), were screened with 32P-labeled total cDNA probes from control (5 degrees C) versus freezing-exposed frogs. Two clones, pBfFR45 and pBfFR04, are reported here in detail and were found to be homologous with the genes for the alpha- and gamma-subunits of fibrinogen, respectively. The clone pBfFR45 carried a 2,305-hp cDNA sequence that was of bipartite structure, containing two open reading frames (ORFs). The first ORF potentially encoded a 332-residue polypeptide, covering a partial sequence of the NH2-terminal region of the alpha-chain. The second ORF encoded a 247-amino acid sequence, covering the whole COOH-terminal region of the alpha-chain; this was highly homologous to the FASORF (fibrinogen-alpha second ORF) of chicken alpha-fibrinogen and the extended alpha-chain of the human protein. Under control (5 degrees C) conditions, moderate levels of fibrinogen alpha- and gamma-transcripts were exclusively found in liver. When frogs were given survivable freezing exposures, levels of these transcripts in liver were highly induced. Transcription of these genes was also elevated in gut and lung during freezing, but mRNA levels in these tissues were lower than in liver. A time course assay confirmed that the transcript levels of both alpha- and gamma-subunit genes were dramatically elevated within the early hours of freezing and reached a maximum threefold increase over control levels after 8 h of freezing exposure. Two other physiological stresses, whole body dehydration and anoxia exposure, mimic individual elements of freezing stress in wood frogs. Northern blot hybridization analysis showed that the expression of both the alpha- and gamma-genes was also upregulated in response to dehydration in vivo (20% of total body water lost), but both were completely inhibited by anoxia exposure.
利用对耐冻林蛙(Rana sylvatica)肝脏构建的cDNA文库进行差异筛选,来寻找冷冻诱导基因。当用来自对照(5℃)与冷冻处理青蛙的32P标记的总cDNA探针,对从冷冻青蛙(在-2.5℃下24小时)肝脏制备的约80,000个cDNA文库噬菌斑进行筛选时,分离出了代表不同基因的5个冷冻反应性cDNA克隆。本文详细报道了两个克隆pBfFR45和pBfFR04,发现它们分别与纤维蛋白原α亚基和γ亚基的基因同源。克隆pBfFR45携带一个2305个碱基对的cDNA序列,其结构为二分体,包含两个开放阅读框(ORF)。第一个ORF可能编码一个332个残基的多肽,覆盖α链NH2末端区域的部分序列。第二个ORF编码一个247个氨基酸的序列,覆盖α链的整个COOH末端区域;这与鸡α纤维蛋白原的FASORF(纤维蛋白原α第二个ORF)和人蛋白质的延伸α链高度同源。在对照(5℃)条件下,仅在肝脏中发现中等水平的纤维蛋白原α和γ转录本。当青蛙接受可存活的冷冻处理时,肝脏中这些转录本的水平被高度诱导。在冷冻过程中,这些基因在肠道和肺中的转录也升高,但这些组织中的mRNA水平低于肝脏。时间进程分析证实,α和γ亚基基因的转录本水平在冷冻的早期数小时内急剧升高,在冷冻暴露8小时后比对照水平达到最大三倍的增加。另外两种生理应激,全身脱水和缺氧暴露,模拟了林蛙冷冻应激的个别因素。Northern印迹杂交分析表明,α和γ基因的表达在体内脱水(全身水分损失20%)时也上调,但两者都被缺氧暴露完全抑制。