Expression of sec18 changes in reponse to changing cellular environments. Below are listed microarrays that clustered sec18 expression with various cellular environments. Explanations for such expression follow the microarrays.
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi
transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
CDC9 |
|
|
nucleotide-excision
repair* |
|
DNA ligase
(ATP) |
|
replication
fork | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
MAG1 |
|
|
not yet
annotated |
|
DNA-3-methyladenine
glycosidase II |
|
not yet
annotated | ||
|
VPS28 |
|
|
not yet
annotated |
|
not yet
annotated |
|
not yet
annotated | ||
|
NOT5 |
|
|
transcription |
|
not yet
annotated |
|
not yet
annotated | ||
|
MSC2 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
NUP85 |
|
|
mRNA-nucleus
export* |
|
structural
protein |
|
nuclear pore | ||
|
RPL34A |
|
|
protein
biosynthesis |
|
structural protein of
ribosome |
|
cytosolic large ribosomal
(60S) subunit | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
RIC1 |
|
|
transcription regulation,
from Pol II promoter* |
|
molecular_function
unknown |
|
nucleus | ||
|
COX12 |
|
|
not yet
annotated |
|
cytochrome-c
oxidase |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
MEF2 |
|
|
protein synthesis
elongation |
|
translation elongation
factor |
|
mitochondrion | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
SEO1 |
|
|
not yet
annotated |
|
not yet
annotated |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
not yet
annotated |
|
not yet
annotated | ||
|
SFT1 |
|
|
intra Golgi
transport |
|
v-SNARE |
|
Golgi
membrane | ||
|
RPS10B |
|
|
protein
biosynthesis |
|
structural protein of
ribosome |
|
cytosolic small ribosomal
(40S) subunit |
|
|
As can be seen here the expression of sec 18 goes up very little in the presence of increasing alpha factor. One would expect that since sec18 is involved in fusion between vesicles of the ER and golgi it would follow that sec18 expression would go up in response to increasing alpha factor. It is known that the receptor for alpha factor is upregulated in response to increasing alpha factor. The alpha-receptor is a tranmembrane protein that must go through the ER and golgo to approach the plasma membrane. Figures were obtained from: <http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi
transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
LUC7 |
|
|
mRNA splice site
selection |
|
small nuclear
ribonucleoprotein |
|
cellular_component
unknown | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
ZTA1 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
APG1 |
|
|
autophagy |
|
protein serine/threonine
kinase |
|
cytosol | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
|
|
|
|
| ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
YPR1 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
MPC54 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
PRC1 |
|
|
not yet
annotated |
|
carboxypeptidase
C |
|
not yet
annotated | ||
|
|
|
|
|
|
|
|
| ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
PTM1 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
IML2 |
|
|
not yet
annotated |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated |
Expression in
response to alpha-factor for SEC18/YBR080C |
|
|
Although the table here would indicate that sec18 expression increases over time in response to alpha factor, as is expected, the microarray data are ambiguous. Induction is not evident because the color change is not dramatic. The figres here were obtained from :<http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
SOL1 |
|
|
not yet annotated |
|
molecular_function unknown |
|
not yet annotated | ||
|
PRD1 |
|
|
not yet annotated |
|
saccharolysin |
|
not yet annotated | ||
|
PTK2 |
|
|
polyamine transport |
|
not yet annotated |
|
not yet annotated | ||
|
RGD1 |
|
|
biological_process unknown |
|
not yet annotated |
|
not yet annotated | ||
|
CDC55 |
|
|
protein biosynthesis* |
|
protein phosphatase type 2A |
|
protein phosphatase type 2A |
The response of sec18 to DNA damaging agents here is not dramatic. Although it would be expected that protein and RNA expression would change in response to a DNA damaging agents, this does not necessarily mean that protein expression would require more traffic between the ER and the golgi. If protein expression changed in favor of cytosolic proteins, there would be no need for a change in sec18 expression. The figres here were obtained from < http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Name |
Score |
Peak
|
|
0.471 |
|
| |
Reference Genes |
| ||
10.9 |
G1 |
| |
10.68 |
S |
| |
3.08 |
G2 |
| |
6.726 |
M |
| |
11.8 |
M/G1 |
| |
|
|
|
|
Plot
of SEC18 (YBR080C) |
|
The data here do not correlate nicely with the literature on sec18 in my opinion. Sec18 is responsible for vacuolar fusion in the yeast daughter cell. One would therefore expect sec18 expression to increase significantly in at lease one phase of cell division so as to mediate vacuolar fusion in the budding yeast daughter. Sec18 is not increased significantly here however. The only explanation for this would be that the quantity of sec18 stays relatively constant at an amount that can sufficiently mediate vacuolar fusion when the time is necessary. Another question that remains is why sec18 would be downregulated during the cell cycle. One possible reason for this would be that there comes a time when vesicular fusion could adversely affect the cell. If all vacuoles fused together at any one time, then one daughter cell would not get the appropriate share of this organelle. The figures here were obtained from this website: < http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi
transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
PRP39 |
|
|
mRNA splicing |
|
not yet
annotated |
|
not yet
annotated | ||
|
SMI1 |
|
|
not yet
annotated |
|
not yet
annotated |
|
not yet
annotated | ||
|
RPN1 |
|
|
ubiquitin-dependent
protein degradation |
|
multicatalytic
endopeptidase |
|
19S proteasome regulatory
particle | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
FMS1 |
|
|
not yet
annotated |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
TAF90 |
|
|
transcription initiation,
from Pol II promoter* |
|
general RNA polymerase II
transcription factor |
|
TFIID
complex* | ||
|
|
|
|
|
|
|
|
| ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
POB3 |
|
|
chromatin
modeling* |
|
molecular_function
unknown |
|
nucleus | ||
|
YRA1 |
|
|
mRNA
processing |
|
not yet
annotated |
|
not yet
annotated | ||
|
IES3 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
SCD6 |
|
|
not yet
annotated |
|
not yet
annotated |
|
not yet
annotated | ||
|
UBC4 |
|
|
stress
response* |
|
ubiquitin conjugating
enzyme |
|
cellular_component
unknown | ||
|
APL6 |
|
|
not yet
annotated |
|
not yet
annotated |
|
not yet
annotated | ||
|
NGL2 |
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
cellular_component
unknown | ||
|
GLO3 |
|
|
ER to Golgi
transport* |
|
ARF GTPase
activator |
|
ER-Golgi intermediate
compartment | ||
|
PAU6 |
|
|
biological_process
unknown |
|
not yet
annotated |
|
not yet
annotated | ||
|
RSG1 |
|
|
biological_process
unknown |
|
not yet
annotated |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
UBP12 |
|
|
deubiquitylation |
|
ubiquitin-specific
protease |
|
cellular_component
unknown |
|
|
|
The data here indicate that sec18 expression does not appreciably change during the diauxic shift. This figure was obtained from <http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi
transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
HOF1 |
|
|
cytokinesis |
|
cytoskeletal protein
binding protein |
|
cytokinetic ring (sensu
Saccharomyces) | ||
|
HMI1 |
|
|
biological_process
unknown |
|
not yet
annotated |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
|
|
|
biological_process
unknown |
|
molecular_function
unknown |
|
not yet
annotated | ||
|
SPT21 |
|
|
transcription |
|
not yet
annotated |
|
not yet
annotated | ||
|
RMA1 |
|
|
not yet
annotated |
|
folylpolyglutamate
synthase |
|
not yet
annotated |
Expression
during sporulation for SEC18/YBR080C |
|
|
The data here indicate that sec18 expression is not changed that much during yeast sporulation. However, a slight induction in the first two hors would seem to be appropriate in that vesicular aggregation and fusion would have to occur to make sure the haploid daughters received their complement of vacuoles and other organelles. The figure here was obtained from <http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi
transport* |
|
adenosinetriphosphatase |
|
cytoplasm* |
The data
here do not represent the full figure from < http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>. A more complete picture of this
information would show that sec18 is variably induced and repressed in response
to different environmental conditions.
One reason why sec18 would be repressed in response to a changing
environmental condition is that proteins in the ER change shape in response to
varying conditions. In response to
heat, for example, proteins can be unfolded and must reside in the ER so they
can refold in their proper confomration (Simola et al., 2000). When this occurs, sec18 is downregulated
so that ER vesicles cannot fuse with the golgi. Conversely, sec18 may be upregulated to
send proteins to the plasma membrane in cases where transmembrane proteins are
denatured as a result of the environmental conditions. The proteins transported to the plasma
membrane with the help of sec18 may replace their misfolded counterparts or aid
the recovery of those proteins that are misfolded.
Orf |
|
Gene |
|
|
|
Process |
|
Function |
|
Component |
|
SEC18 |
|
|
ER to Golgi transport* |
|
adenosinetriphosphatase |
|
cytoplasm* | ||
|
TAT1 |
|
|
transport |
|
amino acid permease |
|
not yet annotated | ||
|
HOM2 |
|
|
not yet annotated |
|
aspartate-semialdehyde dehydrogenase |
|
not yet annotated | ||
|
BNS1 |
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
|
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
VMA21 |
|
|
vacuolar acidification |
|
not yet annotated |
|
not yet annotated | ||
|
YOX1 |
|
|
biological_process unknown |
|
not yet annotated |
|
not yet annotated | ||
|
HTB2 |
|
|
not yet annotated |
|
not yet annotated |
|
nucleosome | ||
|
|
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
PET9 |
|
|
ATP/ADP exchange |
|
ATP/ADP antiporter |
|
mitochondrial inner membrane | ||
|
TIM13 |
|
|
mitochondrial translocation |
|
protein transporter |
|
mitochondrial intermembrane space | ||
|
NUC1 |
|
|
DNA recombination |
|
endodeoxyribonuclease* |
|
mitochondrial inner membrane | ||
|
YCP4 |
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
BAT1 |
|
|
not yet annotated |
|
branched-chain amino acid
aminotransferase |
|
not yet annotated | ||
|
|
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
SUR2 |
|
|
sphingolipid metabolism |
|
sphingosine hydroxylase |
|
endoplasmic reticulum | ||
|
YRA1 |
|
|
mRNA processing |
|
not yet annotated |
|
not yet annotated | ||
|
PDR16 |
|
|
not yet annotated |
|
molecular_function unknown |
|
not yet annotated | ||
|
BAP2 |
|
|
transport |
|
not yet annotated |
|
not yet annotated | ||
|
|
|
|
biological_process unknown |
|
molecular_function unknown |
|
not yet annotated | ||
|
NAB3 |
|
|
mRNA splicing |
|
not yet annotated |
|
not yet annotated |
Expression of sec18 in response to histone depletions
Expression in
response to histone depletion for SEC18/YBR080C |
|
|
The data here indicate that sec18 is eventually downregulated in response to histone depletion. This makes intuitive sense since histones maintain the integrity of DNA. When the structure of DNA risks being disrupted by the loss of histones, protein synthesis should shut down since translated products may contain amino acid irregularities. So as to stop protein traffic, sec18 would naturally be downregulated so that altered proteins made by mistake do not localize to other parts of the cell. The figures here were obtained from < http://genome-www4.stanford.edu/cgi-bin/SGD/expression/expressionConnection.pl>
References Cited
1)
Saccharomyces Genome Database [online database].
Available from: http://genome-www.stanford.edu/Saccharomyces/
Accessed 2001 Oct 17
2) Simola et al. (2000). Trehalose is required for heat-denatured proteins in the yeast ER but not for membrane traffic functions after severe heat stress. Molecular Microbiology; 37 (1); 42-53
Click here to email me at seburke@davidson.edu
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