大鼠肝脏再生增强因子cDNA的克隆及其序列分析
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Cloning and sequence analysis of the rat augmentor of liver regeneration cDNA
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    目的:克隆大鼠肝脏再生增强因子(ALR)cDNA,并对其序列进行分析。方法:建立大鼠2/3肝切除模型,从再生肝组织中提取总RNA,利用RT-PCR技术扩增出大鼠ALRcDNA,亚克隆于pGEM-T载体,并将DNA序列及其推测的氨基酸序列与Genebank作同源性比较。结果和结论:克隆到大鼠ALRcDNA,经核苷酸序列测定证实序列完全正确,其核苷酸序列没有任何突变,它与酵母ERV1cDNA有较高的同源性,核苷酸序列同源性达54.99%,氨基酸序列同源性达47.01%,并发现氨基酸序列中含有锌指蛋白结合区域。

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    Objective: To clone the rat augmentor of liver regeneration (AL R) cDNA and analyse its structure. Methods: The rat ALR cDNA was o btained by using RT-PCR method with total RNA extracted from the regenerating hepatic tissue,then was subcloned into the pGEM-T vector.The sequence of rat A LR cDNA was proved to be correct by sequencing.The rat ALR cDNA and its deduced amino acids sequence were both compared with Genebank database to analyse homol ogy. Results and Conclusion: There isn′t any mutation in cloned r at ALR cDNA.The rat ALR cDNA has higher homology with yeast ERV1 cDNA ,and their homology of DNA and protein is 54.99%and 47.01%respectively. We also find tha t a portion of the rat ALR protein has identity with the binding motif in zinc f inger proteins.

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