首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >Molecular cloning and sequencing of cDNAs encoding homologues of human Ku70 and Ku80 autoantigen from Xenopus and their expression in various Xenopus tissues.
【24h】

Molecular cloning and sequencing of cDNAs encoding homologues of human Ku70 and Ku80 autoantigen from Xenopus and their expression in various Xenopus tissues.

机译:爪蟾人Ku70和Ku80自身抗原同源基因的cDNA的分子克隆和测序及其在多种爪蟾组织中的表达。

获取原文
获取原文并翻译 | 示例
           

摘要

We isolated cDNA clones encoding Ku70 and Ku80 homologues of Xenopus laevis from a cDNA library prepared from Xenopus oocytes. The nucleotide sequences of these Ku70 and Ku80 homologues have coding sequences of 1833 bp and a 611 aa protein, and 2178 bp and a 726 aa protein, respectively. The amino acid sequences deduced from the open reading frame of the Ku70 and Ku80 cDNA clones were highly homologous to those from Ku genes previously isolated, such as human (ca. 65% and ca. 62% identity, respectively) and mouse (ca. 65% and ca. 60%), and show a certain degree of homology to Drosophila (ca. 27% with Ku70), Caenorhabditis elegans (ca. 20% with Ku80) and Saccharomyces cerevisiae (ca. 23% and ca. 19%). Our detailed comparison of the predicted amino acid sequences among these species revealed the highly conserved octa-peptide LPFXXDIR common to both Xenopus Ku70 and Ku80 homologues in the region showing the high homology throughout the species tested. A Northern analysis using specific cDNA probes showed that Ku poly(A)+ mRNAs are expressed at high levels in Xenopus adult oocyte and testis.
机译:我们从非洲爪蟾卵母细胞制备的cDNA文库中分离出编码非洲爪蟾Ku70和Ku80同源物的cDNA克隆。这些Ku70和Ku80同源物的核苷酸序列分别具有1833 bp和611 aa蛋白,2178 bp和726 aa蛋白的编码序列。从Ku70和Ku80 cDNA克隆的开放阅读框推导出的氨基酸序列与先前分离出的Ku基因的氨基酸序列高度同源,例如人类(分别约为65%和62%的同一性)和小鼠(大约50%的同一性)。分别为65%和60%),并且与果蝇(大约70%的Ku70),秀丽隐杆线虫(大约20%的Ku80)和酿酒酵母(大约23%和大约19%)具有一定程度的同源性。 )。我们对这些物种之间预测的氨基酸序列的详细比较揭示了非洲爪蟾Ku70和Ku80同源物共有的高度保守的八肽LPFXXDIR,在整个测试物种中显示出高度的同源性。使用特定cDNA探针的Northern分析表明,Ku poly(A)+ mRNA在非洲爪蟾成年卵母细胞和睾丸中高水平表达。

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