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在鱼类跨亚科克隆胚胎中过表达的新基因K23的鉴定。

Identification of a novel gene K23 over-expressed in fish cross-subfamily cloned embryos.

作者信息

Pei De-Sheng, Sun Yong-Hua, Zhu Zuo-Yan

机构信息

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.

出版信息

Mol Biol Rep. 2009 Jul;36(6):1375-80. doi: 10.1007/s11033-008-9323-3. Epub 2008 Jul 25.

Abstract

A novel gene-K23, differentially expressed in cross-subfamily cloned embryos, was isolated by RACE-PCR technique. It had 2580 base pairs (bp) in length, with a 1,425 bp open reading frame (ORF) encoding a putative protein of 474 amino acids (aa). Bioinformatic analysis indicated that K23 had 22 phosphorylation sites, but it had no signal peptides. Developmental expression analysis in zebrafish showed that K23 transcripts were maternally expressed in ovum and the amount of K23 transcripts increased gradually from zygote to pharyngula period. Subcellular localization analysis revealed that K23 protein was homogeneously distributed both in nuclei and cytoplasm. Taken together, our findings indicate that K23 gene is a novel gene differentially expressed in fish cross-subfamily cloned embryos.

摘要

通过RACE-PCR技术分离出一个在跨亚科克隆胚胎中差异表达的新基因K23。它全长2580个碱基对(bp),有一个1425 bp的开放阅读框(ORF),编码一个由474个氨基酸(aa)组成的假定蛋白质。生物信息学分析表明K23有22个磷酸化位点,但没有信号肽。斑马鱼中的发育表达分析显示,K23转录本在卵子中母源表达,从合子到咽胚期K23转录本的量逐渐增加。亚细胞定位分析表明,K23蛋白在细胞核和细胞质中均匀分布。综上所述,我们的研究结果表明K23基因是一个在鱼类跨亚科克隆胚胎中差异表达的新基因。

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