Possible novel roles of poly(rC)-binding protein 1 in SH-SY5Y neurocytes: an analysis using a dynamic Bayesian network
Objective Poly(rC)-binding protein 1 (PCBP1) belongs to the heterogeneous nuclear ribonucleoprotein family and participates in transcriptional and translational regulation. Previous work has identified transcripts targeted by both knockdown and overexpression of PCBP1 in SH-SY5Y neuroblastoma cells...
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Published in | Neuroscience bulletin Vol. 28; no. 3; pp. 282 - 290 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences
01.06.2012
|
Subjects | |
Online Access | Get full text |
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Summary: | Objective
Poly(rC)-binding protein 1 (PCBP1) belongs to the heterogeneous nuclear ribonucleoprotein family and participates in transcriptional and translational regulation. Previous work has identified transcripts targeted by both knockdown and overexpression of
PCBP1
in SH-SY5Y neuroblastoma cells using a microarray or ProteomeLab™ protein fractionation 2-dimensions (PF-2D) and quadrupole time-of-flight mass spectrometer. The present study aimed to further determine whether these altered transcripts from major pathways (such as Wnt signaling, TGF-β signaling, cell cycling, and apoptosis) and two other genes,
H2AFX
and
H2BFS
(screened by PF-2D), have spatial relationships.
Methods
The genes were studied by qRT-PCR, and dynamic Bayesian network analysis was used to rebuild the coordination network of these transcripts.
Results
PCBP1 controlled the expression or activity of the seven transcripts. Moreover, PCBP1 indirectly regulated
MAP2K2
,
FOS
,
FST
,
TP53
and
WNT7B
through
H2AFX
or regulated these genes through
SAT
. In contrast,
TP53
and
WNT7B
are regulated by other genes.
Conclusion
The seven transcripts and PCBP1 are closely associated in a spatial interaction network. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1673-7067 1995-8218 |
DOI: | 10.1007/s12264-012-1242-6 |