Identification, physical map location and sequence of the denV gene from bacteriophage T4.

Identification, physical map location and sequence of the denV gene from bacteriophage T4.
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噬菌体 T4 中 denV 基因的鉴定、物理图谱位置和序列。

DOI:
10.1093/nar/12.21.8085
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发表时间:
1984
影响因子:
14.9
通讯作者:
J. K. Deriel
J. K. Deriel
中科院分区:
生物学2区
文献类型:
--
作者:
Kristoffer Valerie;E. Henderson;J. K. Deriel

文献摘要

被引文献

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来自噬菌体T4的denV基因,其编码核酸内切酶V,一种小的DNA修复酶,已经通过DNA测序和遗传学相结合的方法被克隆和鉴定,独立于克隆基因的表型效应。对适当的DenV+和DenV-缺失突变体进行物理作图,以精确定义包含denV基因的区域。对该区域进行测序以鉴定denV基因的正确大小的蛋白质编码序列(400-500 bp)。最后,通过对从四个遗传和表型良好表征的denV突变体克隆的相应片段进行测序来确认鉴定。denV基因位于T4基因组上的64 kb处,与ipII基因相邻,并编码138个氨基酸的碱性蛋白质,推断分子量为16,078。
The denV gene from bacteriophage T4, which codes for endonuclease V, a small DNA repair enzyme, has been cloned and identified by an approach combining DNA sequencing and genetics, independent of the phenotypic effect of the cloned gene. Appropriate DenV+ and DenV- deletion mutants were mapped physically to define precisely a region encompassing the denV gene. This region was sequenced in order to identify a protein-coding sequence of the correct size for the denV gene (400-500 bp). Finally, identification was confirmed by sequencing the corresponding fragments cloned from four genetically and phenotypically well-characterized denV mutants. The denV gene is located at 64 kb on the T4 genome, adjacent to the ipII gene, and codes for a basic protein of 138 amino acids with a deduced molecular weight of 16,078.