鸡NF-κB配体受体激活因子(chRANKL)的克隆、表达及生物活性研究

Wang Yan, Hou Jia-fa
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引用次数: 1

摘要

利用逆转录聚合酶链反应(RT-PCR)和重叠延伸基因剪接(SOE-PCR)扩增鸡NF -κB配体受体激活因子(RANKL)的DNA序列,并将其克隆到带his标签的表达质粒pET32a(+)中,在大肠杆菌中高表达。将纯化后的蛋白加入到鸡破骨细胞原代培养中,观察其生物活性。结果表明,PCR产物大小为1 200 bp,与预期一致,诱导蛋白的相对分子量为64 kD。Western blot结果表明,诱导蛋白能与抗his抗体发生反应。还发现诱导蛋白能刺激成熟鸡破骨细胞吸收骨。
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Cloning, expression and bioactivity of chicken receptor activator of NF-κB ligand ( chRANKL )
Using reverse transcription polymerase chain reaction (RT-PCR) and gene splicing by overlap extension (SOE-PCR), the DNA sequence encoding the chicken's receptor activator of NF -κB ligand (RANKL) was amplified, and then cloned into the expressing plasmid pET32a(+) with His-tag, and was highly expressed in Echerichia coli. Then the purified protein was added in primary cultures of chicken osteopclasts to observe its bioactivity. The results showed that the size of PCR product was 1 200 bp which was consistent with the expected one, and the relative molecular weight of induced protein was 64 kD. Western blot indicated that the induced protein could react with anti-His antibody. It was also found that the induced protein could stimulate mature chicken osteoclasts to resorb bone.
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