中华口腔医学研究杂志(电子版) ›› 2008, Vol. 02 ›› Issue (02) : 116 -121. doi: 10.3877/cma.j.issn.1674-1366.2008-02-003
基础研究
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Lan CHENG1, Rong SHU,1
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程岚, 束蓉. 猪牙胚釉原蛋白成熟肽基因原核表达克隆的构建[J/OL]. 中华口腔医学研究杂志(电子版), 2008, 02(02): 116-121.
Lan CHENG, Rong SHU. Construction of prokaryotic expression clone for pig amelogenin gene encoding mature peptide[J/OL]. Chinese Journal of Stomatological Research(Electronic Edition), 2008, 02(02): 116-121.
目的
克隆猪釉原蛋白(pAm)成熟肽编码区基因片段,并构建含有该基因的重组原核表达质粒,为制备基因工程化的重组pAm 奠定基础。
方法
从新生小猪牙胚组织中抽提总RNA,逆转录合成牙胚cDNA,通过PCR 扩增pAm 成熟肽编码序列(约540 bp),所得目的基因插入表达载体质粒PGEX4T1,转化大肠杆菌DH5α。 重组质粒PGEX4T1-pAm 经双酶切和核苷酸序列分析鉴定。
结果
重组质粒PGEX4T1-pAm 经双酶切和测序鉴定证实载体质粒PGEX4T1 中插入的基因片段与pAm 成熟肽基因序列完全相同。
结论
从发育期猪牙胚组织中克隆到釉原蛋白成熟肽编码序列可成功构建含有pAm 成熟肽基因的重组表达质粒。
Objective
To clone pig amelogenin gene encoding mature peptide, and construct prokaryotic expression clone which lay the foundation for expressing the recombinant pig amelogenin in Escherichia coli. in the future.
Methods
Total RNA was extracted from the dental germ of a nascent pig by Trizol. The cDNA fragment of pig Amelogenin gene was obtained with RT-PCR from total RNA. The segment was inserted into prokaryotic gene fusion vector PGEX4T1 and the interesting plasmid was transformed into Escherichia coli. host DH5α. The double-stranded DNA of positive clone was characterized by restriction endonuclease mapping and DNA sequence analysis.
Results
The sequence analysis of recombinant plasmid showed that the pig amelogenin encoding mature protein was inserted into vector PGEX4T1 accurately.
Conclusions
The recombinant prokaryotic expression plasmid PGEX4T1-pAm was successfully constructed by properly inserting pig amelogenin gene encoding mature peptide.