Role of a 19S Proteasome Subunit- PSMD10 in Neurogenesis of Human Neuronal Progenitor Cells.
Clicks: 218
ID: 30566
2019
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Star Article
79.6
/100
208 views
170 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
PSMD10, a proteasome assembly chaperone, is a widely known oncoprotein which aspects many hall mark properties of cancer. However, except proteasome assembly chaperon function its role in normal cell function remains unknown. To address this issue, we induced PSMD10 overexpression in HEK293 cells and the resultant large-scale changes in gene expression profile were analyzed. We constituted networks from microarray data of these differentially expressed genes and carried out extensive topological analyses. The overrecurring yet consistent theme that appeared throughout analysis using varied network metrics is that all genes and interactions identified as important would be involved in neurogenesis and neuronal development. Intrigued we tested the possibility that PSMD10 may be strongly associated with cell fate decisions that commit neural stem cells to differentiate into neurons. Overexpression of PSMD10 in human neuronal progenitor cells facilitated neuronal differentiation via -catenin Ngn1 pathway. Here for the first time we provide preliminary and yet compelling experimental evidence for the involvement of a potential oncoprotein - PSMD10, in neuronal differentiation.
Abstract Quality Issue:
This abstract appears to be incomplete or contains metadata (165 words).
Try re-searching for a better abstract.
| Reference Key |
sahu2019roleinternational
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Sahu, Indrajit;Nanaware, Padma;Mane, Minal;Mulla, Saim Wasi;Roy, Soumen;Venkatraman, Prasanna; |
| Journal | international journal of stem cells |
| Year | 2019 |
| DOI |
10.15283/ijsc19007
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.