Isolation, characterization and expression of the Xenopus laevis ribosomal protein S6 gene

被引:3
作者
Antoine, M [1 ]
Kiefer, P [1 ]
机构
[1] Ruhr Univ Bochum, Fak Med, Abt Virol, Inst Hyg & Med Mikrobiol, D-44780 Bochum, Germany
关键词
gene cloning; housekeeping gene; recombinant DNA; rpS6; promoter;
D O I
10.1016/S0378-1119(99)00100-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report the isolation and characterization of genomic DNA clones encoding Xenopus ribosomal protein (rp) S6. A human rpS6 cDNA was used to screen a genomic DNA library, and this led to the isolation of a genomic clone encompassing the complete rpS6 gene locus. DNA sequencing and primer extension analysis indicate that Xenopus rpS6 is structurally analogous to the mammalian rpS6 genes, and its transcription starts at two sites within the same polypyrimidine tract of 10 bases. A series of deletions of the 5' region of the Xenopus rpS6 gene were fused to the chloramphenicol acetyltransferasereporter gene and transfected into COS-1 cells. The results suggest that the regulatory regions of the Xenopus rpS6 gene are clearly distinct from those earlier reported for the human rpS6 gene, Northern blot analysis of stage-specific embryonic RNA demonstrated an uniform rpS6 transcription during embryogenesis. Southern blot and PCR analyses indicate that the Xenopus rpS6 gene is pseudotetraploid in the Xenopus genome. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
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