Biology Reference
In-Depth Information
IV. CONSERVATION OF CONTROLS
A major reason for using yeasts to study fundamental biological problems is to
exploit the acquired knowledge to understand more complex organisms, espe-
cially humans. In many cases, molecular processes are so complicated in higher
eukaryotes that it is impossible to unravel and understand them, without prior
knowledge from more simple systems. In contrast, in yeasts, the relatively
simplicity of processes permits their characterization, with this information
permitting subsequent analysis and understanding in higher eukaryotes. It has
also been very useful to study the same process in both budding and fission yeasts,
as it has been observed that mechanisms conserved between these two distantly
related organisms, are often conserved in other eukaryotes (C ˆ te
et al.
, 2009;
Forsburg, 1999; Forsburg and Nurse, 1991; Ukil
, 2008).
Among the various genes transcribed at particular cell cycle times, a
number of genes have been shown to be periodically expressed in both budding
and fission yeasts (Table 2.2). Computational analyses have identified up to 20%
of cycling genes encode orthologs that are periodically expressed in both species,
with 5-7% in other eukaryotic organisms (B ¨ hler, 2005a; Lu
et al.
et al.
, 2007).
Table 2.2. Cell Cycle Regulated Genes in Both Budding and Fission Yeasts
Cell cycle
phase
Human
ortholog
Budding yeast
Fission yeast
Function
cdc22 þ
G1-S
RNR1
Ribonucleotide reductase
Yes
cdc18 þ
CDC6
Regulator of DNA replication
Yes
mik1 þ
SWE1
Protein kinase regulating
mitotic entry
Yes
cig2 þ
CLB1-CLB6
B-type cyclins
Yes
pol1 þ
POL1
DNA polymerase
Yes
cdc20 þ
POL2
DNA polymerase e
Yes
S phase
Histone genes
Histone genes
Histones H2A, H2B, H3,
and H4
Yes
plo1 þ
G2-M-G1
phases
CDC5
Polo kinase
Yes
ark1 þ
IPL1
AuroraB kinase
Yes
fin1 þ
KIN3
NimA kinase
Yes
slp1 þ
CDC20
APC regulator
Yes
ace2 þ
ACE2
Cell cycle transcription factor
Yes
mid2 þ
BUD4
Cytokinesis
Yes
spo12 þ
SPO12
Cell cycle regulator
Not known
Representative genes from each cluster are shown, which have significant roles in cell cycle
controls and whose orthologs are also periodically expressed in mammalian cells.
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