Biomedical Engineering Reference
In-Depth Information
Regulatory signals?
(e.g. growth factors, oncogenes)
?
Modified rRNA
ITAFs
H/ACA snoRNPs
NOP10
PUA
domain
Cell growth/proliferation
NHP2
Dyskerin
5'
Ψ
3'
Translation
control of
gene expression
ACA
Ψ
catalytc
domain
Tumor suppression
(OIS/apoptosis)
snoRNA
rRNA
hGAR1
Differentiation/Development
rRNA pseudouridylation
?
Other cis -acting
mRNA elements?
Other RNA substrates?
(e.g. mRNAs)
Frameshift signals
IRES elements
IRES element
3'
X XXY YYZ
5'
ORF
3'
5'
Slippery site
Spacer
Pseudoknot
Fig. 13.5 rRNA pseudouridylation fine-tunes control of gene expression at the translational level. Schematic diagram representing the possible mechanisms
by which pseudouridylation of rRNA may impinge on the translational control of gene expression. rRNA pseudouridylation is carried out by the H/ACA
snoRNP complex; however, the regulatory signals modulating this process remain poorly understood. The incorporation of Y residues ( red ) at specific sites on
rRNA affects the association of the ribosome with highly structured RNA elements including IRES sequences, programmed ribosomal frameshifting signals,
and may also affect the recruitment of additional cis -acting mRNA regulatory elements yet to be identified. Y residues on rRNA may affect the recruitment of
ITAFs and additional factors that enhance translation of specific mRNAs. Recent studies also suggest that other RNA substrates such as mRNA may also be
targeted for pseudouridylation by the H/ACA snoRNPs
 
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