首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Molecular cloning of cDNA encoding a ubiquitin-activating enzyme (E1) from goldfish(Carassius auratus) and expression analysis of the cloned gene
【24h】

Molecular cloning of cDNA encoding a ubiquitin-activating enzyme (E1) from goldfish(Carassius auratus) and expression analysis of the cloned gene

机译:金鱼(Carassius auratus)编码泛素激活酶(E1)的cDNA的分子克隆和克隆基因的表达分析

获取原文
获取原文并翻译 | 示例
       

摘要

Destruction of cyclin B is required to the mitotic and meiotic cycles. a cyclin-specific ubiquitinating system, including ubiquitin-activating enzyme (E1), is thought to be responsible for cyclin B destruction. Here we present the cloning, sequencing and expression analysis of goldfish, Carassius auratus, E1 from goldfish ovary. The cloned cDNA is 4069 bp long and encodes 1059 amino acids. The deduced amino acid sequence is highly homologous to E1 from other species. Recombinant goldfish E1 could transfer ubiquitin to cyclin-selective ubiquitin-conjugating enzyme. Tissue distribution revealed a single 4.0-kb message ubiquitous among tissues.
机译:破坏细胞周期蛋白B是有丝分裂和减数分裂周期所必需的。一个细胞周期蛋白特异性的泛素化系统,包括泛素激活酶(E1),被认为是导致细胞周期蛋白B破坏的原因。在这里,我们介绍了金鱼卵巢中金鱼,assi鱼,E1的克隆,测序和表达分析。克隆的cDNA长4069 bp,编码1059个氨基酸。推导的氨基酸序列与其他物种的E1高度同源。重组金鱼E1可以将泛素转移到细胞周期蛋白选择性泛素结合酶上。组织分布揭示了在组织之间普遍存在的单个4.0kb信息。

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