التفاصيل البيبلوغرافية
| العنوان: |
Dbp5/DDX19 between Translational Readthrough and Nonsense Mediated Decay |
| المؤلفون: |
Christian Beißel, Sebastian Grosse, Heike Krebber |
| المصدر: |
International Journal of Molecular Sciences; Volume 21; Issue 3; Pages: 1085 |
| بيانات النشر: |
Multidisciplinary Digital Publishing Institute |
| سنة النشر: |
2020 |
| المجموعة: |
MDPI Open Access Publishing |
| مصطلحات موضوعية: |
translation, translation termination, mRNA quality control, NMD, Dbp5, Rat8, DDX19, mRNA degradation |
| جغرافية الموضوع: |
agris |
| الوصف: |
The DEAD-box protein Dbp5 (human DDX19) remodels RNA-protein complexes. Dbp5 functions in ribonucleoprotein export and translation termination. Termination occurs, when the ribosome has reached a stop codon through the Dbp5 mediated delivery of the eukaryotic termination factor eRF1. eRF1 contacts eRF3 upon dissociation of Dbp5, resulting in polypeptide chain release and subsequent ribosomal subunit splitting. Mutations in DBP5 lead to stop codon readthrough, because the eRF1 and eRF3 interaction is not controlled and occurs prematurely. This identifies Dbp5/DDX19 as a possible potent drug target for nonsense suppression therapy. Neurodegenerative diseases and cancer are caused in many cases by the loss of a gene product, because its mRNA contained a premature termination codon (PTC) and is thus eliminated through the nonsense mediated decay (NMD) pathway, which is described in the second half of this review. We discuss translation termination and NMD in the light of Dbp5/DDX19 and subsequently speculate on reducing Dbp5/DDX19 activity to allow readthrough of the PTC and production of a full-length protein to detract the RNA from NMD as a possible treatment for diseases. |
| نوع الوثيقة: |
text |
| وصف الملف: |
application/pdf |
| اللغة: |
English |
| Relation: |
Molecular Biology; https://dx.doi.org/10.3390/ijms21031085 |
| DOI: |
10.3390/ijms21031085 |
| الاتاحة: |
https://doi.org/10.3390/ijms21031085 |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| رقم الانضمام: |
edsbas.9C319DA9 |
| قاعدة البيانات: |
BASE |