Key result
Infection of Ehrlich ascites cells with minute virus of mice leads to a general shift in the length of nascent mRNA and a functional reduction in TFIIS-like transcriptional elongation activity.
Why the study?
Does infection with minute virus of mice modify cellular transcription elongation in Ehrlich ascites cells?
Does infection with minute virus of mice modify cellular transcription elongation in Ehrlich ascites cells?
Answers are grounded in this paper and cite their sources.
MVM infection reduces TFIIS-like transcriptional elongation activity in host cells, altering cellular mRNA synthesis.
Our previous observations indicated that upon infection with minute virus of mice (MVM), Ehrlich ascites cells lose a transcription elongation activity which is essential for the readthrough of the MVM attenuator. This was monitored by the ability of extracts from uninfected but not from infected cells to support readthrough of the P4 attenuator when added to partially purified transcription elongation complexes. We have investigated the nature of this change in transcription elongation following MVM infection. In this communication, we show that infection of Ehrlich ascites cells with MVM leads to a general shift in the length of nascent mRNA synthesized in isolated nuclei and separated by sucrose gradients. Furthermore, infection leads to attenuation of transcription of the cellular gene c-fos but not c-myc. We show biochemical evidence to support a model by which, following MVM infection, there is a functional reduction in the activity of a TFIIS-like general transcriptional elongation activity.
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Krauskopf et al. (1994) studied Minute virus of mice (MVM) infection. Minute virus of mice (MVM) infection vs. Uninfected cells was evaluated on Transcription elongation activity and length of nascent mRNA. Infection of Ehrlich ascites cells with minute virus of mice leads to a general shift in the length of nascent mRNA and a functional reduction in TFIIS-like transcriptional elongation activity.
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