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a)
b)
Average mRNA Levels
= Glycolys is; = Oxphos
V_S vs time Plots
= Glycolys is ; = Oxphos
50
1
45
0.9
40
0.8
35
0.7
30
0.6
25
0.5
20
0.4
15
0.3
10
0.2
5
0.1
0
0
0
200
400
600
800
1000
0
200
400
600
800
1000
Time (minute)
Time (minute)
Fig. 12.3. The time courses of the average changes in the transcript level ( TL ) and transcription rate
( TR ) of 12-15 glycolytic ( ) and 14 respiratory genes (
).
12.3.2. Calibration of TR Data
Transcription rates of yeast genes at t 0 were estimated by utilizing the genome-
wide mRNA decay half-lives reported by Wang et al. [32] The half-life data were
down-loaded from their web site ( http://www-genome.stanford.edu/turnover ).
The mathematical relation between transcription rate, dn s,i /dt ,where n s,i is the
number of the i th mRNA molecules synthesized per cell during the time interval
dt ,andthe mRNA i decay half-life, denoted by t 2 ,i , can be derived based on the
following assumptions.
(i)
At t 0 , budding yeast cells are at a steady state with respect to transcription
and transcript degradation. In other words, at t 0 , dn S,i /dt = dn D,i /dt ,
where n D,i is the number of the i th mRNA molecules per cell degraded
during the time interval dt .
The decay of the i th mRNA molecules obeys a first-order rate law given
by
(ii)
dn i /dt = dn D,i /dt = k D,i [ mRNA i ] ,
(12.1)
where k D,i is the first-order degradation rate constant and [ mRNA i ]is
the concentration of the i th mRNA in the cell. Integrating Eq. (12.1) with
respect to time leads to
[ mRNA i ]=[ mRNA i ] 0 e −k D,i t ,
(12.2)
where [ mRNA i ] 0 is the mRNA i abundance at t 0 . Substituting the val-
ues, [ mRNA i ]=[ mRNA i ] 0 / 2 at t = t 2 ,i , and solving the resulting
equation for k D,i yields
k D,i = ln2
t 2 ,i
= 0 . 693
t 2 ,i
.
(12.3)
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