首页> 外文会议>2011 International Conference on Remote Sensing, Environment and Transportation Engineering >Cloning and bioinformatic analysis of full-length cDNA sequence of PsPII in tree peony (Paeonia suffruticosa)
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Cloning and bioinformatic analysis of full-length cDNA sequence of PsPII in tree peony (Paeonia suffruticosa)

机译:牡丹(Peonia suffruticosa)PsPII全长cDNA序列的克隆及其生物信息学分析。

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In this study, using RACE-PCR method, the full-length cDNA of PsPII gene from cold-stress Lu Hehong buds was obtained and sequenced. The amplified fragment length of 5′RACE-PCR was 439bp and the full-length cDNA was 899bp, containing an open reading frame of 603bp, which encoded a 200 amino acid polypeptide. PII protein of tree peony was non-secretory and hydrophilic, and no had transmembrane domain. Its main secondary structure element was alpha helix. The prediction of subcellular localization showed that PsPII gene was located in the cytoplasm. Using the methods of bioinformatics, predictions of functional domains revealed that the expression of PII was linked to the level of nitrogen in the cell and PII protein was capable of sensing the level of C/N. By BLASTN, nitrogen regulatory protein PII modulated the activity of glutamine synthetase.
机译:本研究采用RACE-PCR方法,从寒冷胁迫下的陆鹤红芽中获得了PsPII基因的全长cDNA,并进行了测序。 5'RACE-PCR的扩增片段长度为439bp,全长cDNA为899bp,含有603bp的开放阅读框,编码200个氨基酸的多肽。牡丹的PII蛋白是非分泌性的,亲水性的,没有跨膜结构域。它的主要二级结构元素是α螺旋。亚细胞定位的预测表明PsPII基因位于细胞质中。使用生物信息学方法,对功能域的预测显示,PII的表达与细胞中的氮水平相关,而PII蛋白能够感知C / N的水平。通过BLASTN,氮调节蛋白PII调节了谷氨酰胺合成酶的活性。

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