Allard A, Wadell G
Department of Virology, University of Umeå, Sweden.
Virology. 1992 May;188(1):319-30. doi: 10.1016/0042-6822(92)90761-d.
Enteric adenovirus type 41 (Ad41) is defective for growth in conventional established cell lines. Ad41 is dependent on the Ad5 early regions E1A/E1B since it cannot grow in HEK cells but only in 293 HEK cells transformed by Ad5 E1 region. However, Hep-2 cells have also been shown to support the growth of Ad41 to some extent. The nucleotide sequence of the E1B region of the Ad41 strain D389 has been determined. When compared to the corresponding region of the Ad41 prototype strain (Tak) the degree of homology in the DNA sequences was close to 100%. The mRNAs from the E1B region of the Ad41 strain D389 have been studied by Northern blot, primer extension, and polymerase chain reaction-cDNA analysis. E1B transcripts corresponding to Ad2 14 S, 22 S, and 9 S mRNAs were identified but no 13 S mRNA equivalent was detected, a pattern similar to that seen in the Ad40 and Ad12 transcription maps. However, the Ad41 E1B 14S mRNA equivalent has one additional small exon of 23 nucleotides, created by a donor and an acceptor splice site located at positions not seen in other E1B transcripts of human adenoviruses analyzed so far. The coding potential for E1B 19K, 55K, and 15K proteins and for pIX is retained in the Ad41 transcripts. In contrast to other adenoviruses, except for the closely related Ad40, the ORF of pIX starts in the intron of the 22 S mRNA.
肠道腺病毒41型(Ad41)在传统的已建立细胞系中生长存在缺陷。Ad41依赖于腺病毒5型(Ad5)的早期区域E1A/E1B,因为它不能在人胚肾(HEK)细胞中生长,而只能在由Ad5 E1区域转化的293 HEK细胞中生长。然而,已证明Hep-2细胞在一定程度上也支持Ad41的生长。已确定Ad41 D389株E1B区域的核苷酸序列。与Ad41原型株(Tak)的相应区域相比,DNA序列中的同源程度接近100%。通过Northern印迹、引物延伸和聚合酶链反应 - cDNA分析研究了Ad41 D389株E1B区域的信使核糖核酸(mRNA)。鉴定出了与Ad2 14 S、22 S和9 S mRNA相对应的E1B转录本,但未检测到相当于13 S mRNA的转录本,这一模式与在Ad40和Ad12转录图谱中看到的相似。然而,相当于Ad41 E1B 14S mRNA的转录本有一个额外的23个核苷酸的小外显子,它由一个供体和一个受体剪接位点产生,这两个位点位于迄今为止分析的人类腺病毒其他E1B转录本中未出现的位置。Ad41转录本中保留了E1B 19K、55K和15K蛋白以及pIX的编码潜能。与其他腺病毒不同,除了密切相关的Ad40外,pIX的开放阅读框(ORF)起始于22 S mRNA的内含子中。