Beschreibung
Produktdetails
Format
Kopierschutz
Nein
Family Sharing
Ja
Text-to-Speech
Nein
Erscheinungsdatum
24.11.2017
Verlag
Cuvillier Verlag eBooksSeitenzahl
152 (Printausgabe)
Dateigröße
3373 KB
Sprache
Englisch
EAN
9783736985896
A large coiled-coil protein, Tpr (Translocated promoter region) is located at the nuclear side of the nuclear pore complex (NPC), and plays an important role in the architecture of the nuclear basket (NB). Although its contribution to the NB structure has been characterized, little is known about the function of Tpr. In this work, we investigated whether and how Tpr contributes to the surveillance of mRNA export, especially, to the quality control (QC) of certain un-spliced mRNAs.
To answer these questions, we established a series of different reporter cell lines, allowing us to monitor the occurrence of un-spliced and spliced reporter transcripts. In the analysis of most of these reporter cell lines, the depletion of Tpr did not cause any obvious leakage of un-spliced reporter mRNAs. However, when the coding sequence of the HIV (Human immunodeficiency virus) Gag protein was used as a readout, the cytoplasmic levels of the un-spliced HIV-gag mRNAs were highly enhanced in the absence of Tpr. Such phenotype was only observed when a viral RNA export enhancer element, the CTE (the constitutive transport element), that recruits the general mRNA export receptor, NXF1/TAP, was part of the HIV-gag reporter gene. Intriguingly, a slight reduction in the cellular Tpr levels already caused the breakdown of a retention mechanism that normally keeps these HIV-gag transcripts in the nucleus. Results obtained with this and other transcripts showed that Tpr can indeed play a role in keeping certain transcripts within the nucleus in an export-pathway-dependent manner. However, they also reveal that this Tpr-dependent retention mechanism does not monitor intron-containing transcripts in general. In fact, at least in the case of the HIV-gag transcript, such retention did not depend on the presence of splice sites, the branch point sequence (BPS), or the poly-pyrimidine track (PPT). How such retention of certain transcripts along a distinct export pathway might be mechanistically explainable is being discussed.
To answer these questions, we established a series of different reporter cell lines, allowing us to monitor the occurrence of un-spliced and spliced reporter transcripts. In the analysis of most of these reporter cell lines, the depletion of Tpr did not cause any obvious leakage of un-spliced reporter mRNAs. However, when the coding sequence of the HIV (Human immunodeficiency virus) Gag protein was used as a readout, the cytoplasmic levels of the un-spliced HIV-gag mRNAs were highly enhanced in the absence of Tpr. Such phenotype was only observed when a viral RNA export enhancer element, the CTE (the constitutive transport element), that recruits the general mRNA export receptor, NXF1/TAP, was part of the HIV-gag reporter gene. Intriguingly, a slight reduction in the cellular Tpr levels already caused the breakdown of a retention mechanism that normally keeps these HIV-gag transcripts in the nucleus. Results obtained with this and other transcripts showed that Tpr can indeed play a role in keeping certain transcripts within the nucleus in an export-pathway-dependent manner. However, they also reveal that this Tpr-dependent retention mechanism does not monitor intron-containing transcripts in general. In fact, at least in the case of the HIV-gag transcript, such retention did not depend on the presence of splice sites, the branch point sequence (BPS), or the poly-pyrimidine track (PPT). How such retention of certain transcripts along a distinct export pathway might be mechanistically explainable is being discussed.
Kundinnen und Kunden meinen
Verfassen Sie die erste Bewertung zu diesem Artikel
Helfen Sie anderen Kund*innen durch Ihre Meinung
Kurze Frage zu unserer Seite
Vielen Dank für dein Feedback
Wir nutzen dein Feedback, um unsere Produktseiten zu verbessern. Bitte habe Verständnis, dass wir dir keine Rückmeldung geben können. Falls du Kontakt mit uns aufnehmen möchtest, kannst du dich aber gerne an unseren Kund*innenservice wenden.
zum Kundenservice