عنوان
پدید آورنده
موضوع
رده
کتابخانه
محل استقرار
TL11t5w9pt
انگلیسی
Characterization of the archaebacterial ortholog of the processing body subunit Winnebago/Growl
[Thesis]
Motamedi, Amir
UC San Diego
2010
UC San Diego
2010
Because the transcriptional machinery is inactive throughout late stages of oogenesis and early stages of embryogenesis, the initial development of the embryo is driven by post-transcriptional regulation of maternally deposited mRNA. In Drosophila, this post-transcriptional regulation occurs at specialized sites called P- bodies. While P bodies contain proteins required for mRNA degradation, translational control, and microRNA processing, the complete composition of the P body is unknown. Recent work on the biochemistry of the P body has identified a novel protein of unknown function called Winnebago. Winnebago contains an atypical conserved ATPase motif homologous with the cyclo-ligase human methenyltetrahydrofolate synthetase (MTHFS) and a conserved RNA recognition motif suggesting that Winnebago may be a novel RNA modifying enzyme. Consistent with this, the substrate binding site of the Winnebago and its archaebacterial homologs are not conserved with the human MTHFS, indicating that Winnebago has a unique class of substrate. In this study, Swinn, the Winnebago homolog from Sulfolobus, was purified and it was demonstrated that it is an ATPase. We also found that Swinn does not use the normal substrates of MTHFS, arguing that it acts on a novel class of cyclo-ligase substrates. This work lays the groundwork for future studies to identify the substrate of the Winnebago family of ATPases and their role in RNA regulation
Motamedi, Amir
UC San Diego
مطالعه متن کتاب p
[Thesis]
276903
a
Y
