Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.4.25.1 (
proteasome
)
28,817
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Nob1p is a nuclear protein that forms a complex with the 19S regulatory particle of the 26S
proteasome
and with uncharacterized nuclear protein Pno1p. Overexpression of NOB1 overrode the defects in maturation of the 20S
proteasome
of ump1Delta cells, and temperature-sensitive nob1 and pno1 mutants exhibited defects in the processing of the beta subunits and in the assembly of the 20S and the 26S proteasomes. A defect in either NOB1 or
PNO1
caused accumulation of newly formed Pre6p in the cytoplasm, whereas Pre6p of the ump1Delta strain accumulated in the nucleus irrespective of the temperature. Here we present a model proposing that (1) Nob1p serves as a chaperone to join the 20S
proteasome
with the 19S regulatory particle in the nucleus and facilitates the maturation of the 20S
proteasome
and degradation of Ump1p, and (2) Nob1p is then internalized into the 26S
proteasome
and degraded to complete 26S
proteasome
biogenesis.
...
PMID:Nob1p is required for biogenesis of the 26S proteasome and degraded upon its maturation in Saccharomyces cerevisiae. 1250 37
PNO1
(partner of Nob1) was known as a RNA-binding protein in humans, and its ortholog
PNO1
was reported to participate ribosome and
proteasome
biogenesis in yeasts. Yet there have been few studies about its functions in mammalian cells, and so far its role in human cells has never been reported, especially in urinary bladder cancer (UBC).We interrogated the cellular functions and clinical significance of
PNO1
in, and its molecular mechanism through microarrays and bioinformatics analysis. Our findings support that
PNO1
participates in promoting proliferation and colonogenesis, while reducing apoptosis of UBC cells, and is also predicted to be associated with the migration and metastasis of UBC
PNO1
knockdown (KD) attenuated the tumorigenesis ability of UBC in mouse.
PNO1
KD led to the altered expression of 1543 genes that are involved in a number of signalling pathways, biological functions and regulation networks. CD44, PTGS2, cyclin D1, CDK1, IL-8, FRA1, as well as mTOR, p70 S6 kinase, p38 and Caspase-3 proteins were all down-regulated in
PNO1
KD cells, suggesting the involvement of
PNO1
in inflammatory responses, cell cycle regulation, chemotaxis, cell growth and proliferation, apoptosis, cell migration and invasiveness. This study will enhance our understanding of the molecular mechanism of UBC and may eventually provide novel targets for individualized cancer therapy.
...
PMID:Importance of PNO1 for growth and survival of urinary bladder carcinoma: Role in core-regulatory circuitry. 3180 Jan 62