首页> 外文期刊>African Journal of Biotechnology >cDNA, genomic sequence cloning and overexpression of ribosomal protein S16 gene (RPS16) from the Giant Panda
【24h】

cDNA, genomic sequence cloning and overexpression of ribosomal protein S16 gene (RPS16) from the Giant Panda

机译:来自巨型熊猫的核糖体蛋白S16基因(RPS16)的cDNA,基因组序列克隆和过度表达

获取原文
获取外文期刊封面目录资料

摘要

RPS16?of?eukaryote?is a component of the 40S small ribosomal subunit encoded byRPS16?gene and is also a homolog of prokaryotic?RPS9. The cDNA and genomic sequence of RPS16 was cloned successfully for the first time from the Giant Panda (Ailuropoda melanoleuca) using reverse transcription-polymerase chain reaction (RT-PCR) technology?and Touchdown-PCR, respectively, which were both sequenced and analyzed preliminarily. The cDNA of the?RPS16?gene was overexpressed in?Escherichia coli?BL21.?The length of cDNA fragment cloned is 448 bp containing an open reading frame of 441 bp encoding 146 amino acids and the length of the genomic sequence is 2510 bp, containing five exons and four introns.?Alignment analysis indicates that the nucleotide sequence share a high homology with those of?Bos taurus,?Homo sapiens,?Mus musculus,?Rattus norvegicus?and?Danio rerio?by?95.46,?92.97, 89.80, 89.80 and?82.54%, respectively.The deduced amino acid sequence is entirely identical compared with the first four animals and share a high homology with that of?D. rerio?by 96.58%. Topology prediction shows that there is one cAMP- and cGMP-dependent protein kinase phosphorylation site, three protein kinase C phosphorylation sites, one casein kinase II phosphorylation site, two N-myristoylation sites, one amidation site and one ribosomal protein S9 signature in the?RPS16?protein of the Giant Panda . TheRPS16?gene can be readily expressed in?E. coli?and it fused with the N-terminally GST-tagged protein which gave rise to the accumulation of an expected 20.095 kDa polypeptide, in good agreement with the predicted molecular weight. The expression product obtained could be used for purification and further study of its function.
机译:RPS16?真核生物?是40s小核糖体亚基的组分,伯普斯16α基因,也是原核感染的同源物。使用逆转录 - 聚合酶链反应(RT-PCR)技术(RT-PCR)技术,首次从巨熊猫(Ailuropoda Melanoleuca)中成功地克隆了RPS16的cDNA和基因组序列?分别进行测序和初步分析。 rps16的cDNA?基因在αscherichiacoliΔbl21中过表达。克隆的cDNA片段的长度是448bp,含有441bp的开放读数框架,编码146氨基酸的长度为2510bp,含有五个外显子和四个内部内外节.?Aligmment分析表明核苷酸序列与那些博士群岛的核苷酸序列与?莫达·斯帕森,?Mus Musculus,?rattus norvegicus?和?danio rerio?by?95.46,?92.97, 89.80,89.80和?82.54%分别。推导的氨基酸序列与前四只动物相比完全相同,并与Δd的高同源性。雷丽奥?达到96.58%。拓扑预测表明,存在一个营养和CGMP依赖性蛋白激酶磷酸化位点,三种蛋白激酶C磷酸化位点,一个酪蛋白激酶II磷酸化位点,两个N-Myr脲位点,一次酰胺位点和一个核糖体蛋白S9签名? rps16?巨大的熊猫蛋白质。 Therps16?基因可以容易地表达?e。 COLI?它与N-末端GST标记的蛋白质融合,其与预测的分子量良好地产生预期的20.095kDa多肽的积累。所得表达产物可用于纯化和进一步研究其功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号