This is an assignment for an undergraduate course at Davidson
College
The text below discusses the clustering of sec18 with other genes under
certain environmental conditions. sec18 is a protein
that mediates vesicular fusion between vacuolar fragments during mitosis
and between ER and golgi vesicles during the
transport of proteins. For a full report of the expression of
sec18 in response to various environmental and cellular conditions,
go to this website and run a search with sec18
<http://genome-www4.Stanford.EDU/cgi-bin/SGD/expression/expressionConnection.pl>.
The clustering should appear similar
to this for the clustering of sec18 with other genes in response to
alpha factor.
I) Response to alpha factor
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 golgi to approach the plasma membrane.
II) Response to DNA damaging agent
sec18 does not respond drastically to DNA damaging
agents. Although there are other proteins that seem to change their
expression dramatically, one would not expect the expression of sec18
to change unless most of the proteins being induced
were going to be secreted or unless thos proteins were transmembrane
proteins. If the protein expression changed in favor of
cytosolic proteins, then sec18 would not have to be upregulated because
protein traffic between the ER and the gologi would
either stay the same or decrease.
III) Expression of sec18 during the cell cycle.
The expression of sec18 during the cell cycle in the microarray
data at
<http://genome-www4.Stanford.EDU/cgi-bin/SGD/expression/expressionConnection.pl>
does not correlate with the literature
on sec18.. 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
however. The only explanation for this would be that the quantity
of sec18 stays relativelyconstant 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 vacuolesfused together
in S phase for example, then one daughter cell would not get the appropriate
share of this organelle after division.
IV) Expression of sec18 during sporulation
The data here indicate that sec18 expression
is not changed that much during yeast sporulation. However, a slight
induction
idoes occur and 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.
V) Expression of sec18 in response to changing environmental conditions
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). Trehalose mediates
the proper refolding of proteins in the ER. When a return to
proper folding occurs for proteins in the ER, sec18 is downregulated
so that ER vesicles cannot fuse with the golgi. If sec18
did mediate fusion between the ER and the golgi while proteins were
misfolded, proteins would be transported to cellular
locations only to be non-functional. Protein structure indeed
equals function! 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. Such
a scenario could explain the inductions of sec18 in response to
changing environmental conditions.
VI) Expression of sec18 in response to histone depletion
sec18 is downregulated in response to
histone depletion. This makes intuitive sense since histones maintain
the integrity
ofDNA. 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 get transported to
other parts of the cell.
VII) Other expression patterns of sec18
The expression pattern of sec18 does not change
drastically during a diauxic shift from an aerobic to an anaerobic
environment. sec18 neither changes its expression significantly
in tup deletions or Yal overexpression.
References Cited
1) Saccharomyces Genome Database [online
database]. Available from:
<http://genome-www4.Stanford.EDU/cgi-bin/SGD/expression/expressionConnection.pl>
Accessed 2001 Oct17
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
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