Control of adenovirus E1B mRNA synthesis by a shift in the activities of RNA splice sites

التفاصيل البيبلوغرافية
العنوان: Control of adenovirus E1B mRNA synthesis by a shift in the activities of RNA splice sites
المؤلفون: Marvin H. Caruthers, E F Fisher, A J Berk, Craig Montell
المصدر: Molecular and Cellular Biology. 4:966-972
بيانات النشر: Informa UK Limited, 1984.
سنة النشر: 1984
مصطلحات موضوعية: Messenger RNA, Splice site mutation, RNA splicing, P-bodies, Intron, splice, Cell Biology, Biology, Primary transcript, Precursor mRNA, Molecular Biology, Molecular biology
الوصف: The primary transcript from adenovirus 2 early region 1B (E1B) is processed by differential RNA splicing into two overlapping mRNAs, 13S and 22S. The 22S mRNA is the major E1B mRNA during the early phase of infection, whereas the 13S mRNA predominates during the late phase. In previous work, it has been shown that this shift in proportions of the E1B mRNAs is influenced by increased cytoplasmic stability of the 13S mRNA at late times in infection. Two observations presented here demonstrate that the increase in proportion of the 13S mRNA at late times is also regulated by a change in the specificity of RNA splicing. First, the relative concentrations of the 13S to 22S nuclear RNAs were not constant throughout infection but increased at late times. Secondly, studies with the mutant, adenovirus 2 pm2250 , provided evidence that there was an increased propensity to utilize a 5' splice in the region of the 13S 5' splice site at late times in infection. Adenovirus 2 pm2250 has a G----C transversion in the first base of E1B 13S mRNA intron preventing splicing of the 13S mRNA but not of the 22S mRNA. During the early phase of a pm2250 infection, the E1B primary transcripts were processed into the 22S mRNA only. However, during the late phase, when the 13S mRNA normally predominates, E1B primary transcripts were also processed by RNA splicing at two formerly unused or cryptic 5' splice sites. Both cryptic splice sites were located much closer to the disrupted 13S 5' splice site than to the 22S 5' splice site. Thus, the temporal increase in proportion of the 13S mRNA to the 22S mRNA is regulated by two processes, an increase in cytoplasmic stability of the 13S mRNA and an increased propensity to utilize the 13S 5' splice site during the late phase of infection. Adenovirus 2 pm2250 was not defective for productive infection of HeLa cells or for transformation of rat cells.
تدمد: 1098-5549
0270-7306
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3fcd4065831610c6632471913e0a3e77Test
https://doi.org/10.1128/mcb.4.5.966Test
حقوق: OPEN
رقم الانضمام: edsair.doi...........3fcd4065831610c6632471913e0a3e77
قاعدة البيانات: OpenAIRE