Braithwaite A W, Diver W P, Le Jeune S, Driver F, Naora H
Chromosoma. 1986;93(6):537-44. doi: 10.1007/BF00386796.
Previous studies suggesting homology between human cellular DNA and the DNAs from adenovirus types 2 and 5 are extended in the present paper. A clone (ChAdh), isolated from a human genomic DNA library using an adenovirus probe, hybridized to discrete regions of adenovirus 2 DNA, including part of the transforming genes E1a and E1b, as well as to repeated sequences within human DNA. The E1a and E1b genes both hybridize to the same 300 base pair Sau3AI fragment within ChAdh although there is no obvious homology between E1a and E1b. The Ad 2 E1a gene was also used as a probe to screen other cellular DNAs to determine whether repeated sequences detectable with Ad2 DNA probes were conserved over long evolutionary periods. Hybridization was detected to the genomes of man, rat, mouse and fruit fly, but not to those of yeast and bacteria. In addition to a "smear" hybridization, discrete fragments were detected in both rodent and fruit fly DNAs. The experiments reported suggest the existence of two different types of cellular sequences detected by Ad 2 DNA: (1) repeated sequences conserved in a variety of eukaryote genomes and (2) a possible unique sequence detected with an E1a probe different from that responsible for hybridization to repeated sequences. This unique sequence was detected as an EcoRI fragment in mouse DNA and had a molecular size of about 8.8 kb.
先前的研究表明人类细胞DNA与2型和5型腺病毒的DNA之间存在同源性,本文对此进行了扩展。使用腺病毒探针从人类基因组DNA文库中分离出一个克隆(ChAdh),它与腺病毒2 DNA的离散区域杂交,包括部分转化基因E1a和E1b,以及人类DNA中的重复序列。尽管E1a和E1b之间没有明显的同源性,但E1a和E1b基因都与ChAdh内相同的300个碱基对的Sau3AI片段杂交。腺病毒2 E1a基因也被用作探针来筛选其他细胞DNA,以确定用腺病毒2 DNA探针可检测到的重复序列在长期进化过程中是否保守。在人类、大鼠、小鼠和果蝇的基因组中检测到杂交信号,但在酵母和细菌的基因组中未检测到。除了“拖尾”杂交外,在啮齿动物和果蝇的DNA中都检测到了离散的片段。报道的实验表明,腺病毒2 DNA检测到两种不同类型的细胞序列:(1)在多种真核生物基因组中保守的重复序列;(2)用E1a探针检测到的一种可能独特的序列,它与负责与重复序列杂交的序列不同。这种独特的序列在小鼠DNA中被检测为一个EcoRI片段,分子大小约为8.8 kb。