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小鼠核心结合因子1成熟肽编码区的cDNA克隆和序列测定
引用本文:余擎,肖明振,吴补领,田宇,郭红延. 小鼠核心结合因子1成熟肽编码区的cDNA克隆和序列测定[J]. 牙体牙髓牙周病学杂志, 2002, 12(3): 121-123
作者姓名:余擎  肖明振  吴补领  田宇  郭红延
作者单位:第四军医大学口腔医学院,陕西,西安,710032
基金项目:全军“十五”计划基金重点课题 ( 0 12 0 89),全军骨干青年教师资助项目
摘    要:
目的:研究核心结合因子1(cbfal)在小鼠牙胚组织中的表达,扩增cbfal成熟肽编码区的特异性片段,构建重组质粒,为进一步的蛋白表达、抗体制备、基因转染等研究奠定基础。方法:提取新生小鼠的颅骨、牙胚、肝脏组织总RNA,反转录为cDNA后进行PCR反应,构建pGEM-cbfal重组质粒并测序。结果:从小鼠颅骨和牙胚组织中均获得了约1791bp的目的片段,牙胚来源的PCR产物的测序结果证实成功地克隆到了cbfal成熟肽编码区,酶切结果显示重组质粒构建成功。结论:新生小鼠的牙胚组织中有cbfal基因的表达。

关 键 词:cDNA克隆 序列测定 小鼠 核心结合因子 聚合酶链式反应 蛋白表达 抗体制备
文章编号:1005-2593(2002)03-0121-03
修稿时间:2001-10-22

Cloning and sequencing of the coding region of mouse cbfa1 gene
YU Qing,XIAO Ming-zhen,WU Bu-ling,et al. Cloning and sequencing of the coding region of mouse cbfa1 gene[J]. Chinese Journal of Conservative Dentistry, 2002, 12(3): 121-123
Authors:YU Qing  XIAO Ming-zhen  WU Bu-ling  et al
Abstract:
AIM: To observe the expression of cbfa1 in mouse tooth germs, to clone and sequence the cDNA of cbfa1 from mouse tooth germs. METHODS: Total RNA was isolated from newborn mouse tooth germs tissue and reverse-transcribed into cDNA. The desired DNA product was obtained by PCR with two cbfa1 specific primers. The segment was inserted into pGEM-5zf vector and the positive clone was sequenced by Takara Corporation. RESULTS: cDNA of cbfa1 was obtained from mouse tooth germs tissue. The sequence was consistent with that displayed on Pubmed. No mutation was found. CONCLUSION: This study provides the evidence of expression of cbfa1 in mouse tooth germs tissue.
Keywords:mouse  cbfa1  PCR
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