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When a cell has grown to its maximum size it divides , 
and it take place a series of changes in a newly formed 
cell which involve in growth and division to form 2 
daughter cells , it is called Cell cycle. 
It consist of two stages, 
A non dividing growing Interphase Or I Phase 
A Short Dividing Mitotic/ M Phase
 The period between two mitotic divisions is called 
Interphase . 
It is further divisible into 3 stages: 
1. • G1 phase 
2. • S phase 
3. • G2 phase
G1 phase : 
 It is the post mitotic phase and takes place at the end of cell division 
the newly formed cells accumulate the energy and prepares 
themselves for the synthesis of DNA . During this , active synthesis 
of RNA and protein takes place . 
S phase : 
 It is the synthesis phase during this phase duplication of DNA and 
centriole takes places. The duplication of DNA results in the 
duplication of chromosomes . 
G2 phase : 
 It is the pre- mitotic gap phase (invisible phase) the synthesis of 
RNA and protein continues in this phase. The formation of macro 
molecules for spindle formation takes place and the cell prepare it 
self to go into the mitotic phase .
MITOTIC PHASE 
M Phase follows the interphase. This last for a shot period compare to 
interphase .During this phase two important processes occur simultaneously 
they are 
karyokinesis (division of nucleus) : 
It results in the separation of chromosomes into two equal groups . 
Cytokinesis (division of cytoplasm) : 
It results in division of cytoplasmic components into approximately two halves. 
After M phase a cell may either enter interphase to repeat the cell cycle or G0 
phase to arrest the cell cycle. The cells in G0 phase may grow in size and get 
differentiated .
A checkpoint in the 
cell cycle is a critical 
control point where 
stop and go signals 
regulate the cycle. 
3 major checkpoints 
are found in the G1, 
G2, and M phases.
Regulation of the Cell Cycle: 
Cell Cycle Checkpoints
G2 Checkpoint Control by MPF 
 Active MPF = Mitotic Cdk + mitotic cyclin 
 Cdk is cyclin-dependant kinase 
 MPF controls G2  M by phosphorylating and activating 
proteins involving in: 
Chromosome condensation 
Nuclear envelope breakdown 
Spindle assembly 
It’s own self-destruction
G2 checkpoint
G1 checkpoint 
• Controlled by G1 Cdks-cyclin 
• G1 cyclin levels also 
vary with the cell cycle 
• Many additional levels of 
phosphorylation, 
dephosphorylation 
regulate.
• The Cell Cycle Is Regulated by Protein Kinases. 
• The mechanism regulating the progression of cells 
through their division cycle is highly conserved in 
evolution, and plants have retained the basic 
components of this mechanism. 
• The key enzymes that control the transitions 
between the different states of the cell cycle, and the 
entry of nondividing cells into the cell cycle, are the 
cyclin-dependent protein kinases, or CDKs
 Cell division is a vital process that requires orderly 
progression . 
 Endogenous hormones such as auxin,cytokinins, 
abscisic acid, gibberellins and brassinosteroids as 
well as environmental factors all regulate progression 
through the cell cycle. 
 cell cycle events take place with clock-like precision . 
Recent studies have demonstrated that cell cycles in 
plants and animals are regulated by similar mechanisms. 
 A group of highly conserved serine/threonine kinases 
called cyclin-dependent kinases(CDKs) has been 
found to play a key role in guiding the cell cycle process.
Four classes of cyclins : 
1. G1-cyclins — help to promote passage through “ Start” or the 
restriction point in late G1 
2. G1/S-cyclins — bind Cdks at the end of G1 and commit the 
cell to DNA replication 
3. S-cyclins – binds Cdks during S phase and are required for 
the initiation of DNA replication 
4. M-cyclins — promote the events of mitosis
• Protein kinases are enzymes that phosphorylate proteins 
using ATP. 
• The regulated activity of CDKs is essential for the transitions 
from G1 to S and from G2 to M, and for the entry of 
nondividing cells into the cell cycle. 
• The transition from G1 to S requires a set of cyclins ( G1 
cyclins) different from those required in the transition from 
G2 to mitosis, where mitotic cyclins activate the CDKs . 
• CDKs possess two tyrosine phosphorylation sites: One 
causes activation of the enzyme; the other causes 
inactivation. 
• Specific kinases carry out both the stimulatory and the 
inhibitory phosphorylation
• Similarly, protein phosphatases can remove 
phosphate from CDKs, either stimulating or inhibiting 
their activity, depending on the position of the 
phosphate. 
• The addition or removal of phosphate groups from 
CDKs is highly regulated and an important mechanism 
for the control of cell cycle progression . 
• Cyclin inhibitors play an important role in regulating the 
cell cycle in animals, and probably in plants as well, 
although little is known about plant cyclin inhibitors.
CDK activity can be regulated in various ways, but two of 
the most important mechanisms are 
(1) cyclin synthesis and destruction and 
(2) the phosphorylation and dephosphorylation of key 
amino acid residues within the CDK protein.
• CDKs are inactive unless they are associated with a cyclin. 
Most cyclins turn over rapidly. 
• They are synthesized and then actively degraded (using ATP) 
at specific points in the cell cycle. 
• Cyclins are degraded in the cytosol by a large proteolytic 
complex called the proteasome. 
• Before being degraded by the proteasome, the cyclins are 
marked for destruction by the attachment of a small protein 
called ubiquitin, a process that requires ATP.
 G2-M transition is also a major control point. Both A-type and B-type 
CDKs are thought to be involved in this process. 
 A-type CDKs are expressed constitutively, while the plant-specific B-type 
CDKs increase expression during the G2-M transition point. 
 CDKA and CDKB subunits interact with their respective cyclin 
partners (CycA/B). 
 Both the expression of CDKA/B and CycA/B genes and the activity of 
CDKA/B kinases are affected by plant hormones. 
 Auxin, GA and cytokinin increase expression of these genes, and 
cytokinin can also induce removal of an inhibitory phosphate group 
(T14/Y15) on CDKA/B subunits. 
 In an additional level of control, phosphorylation at a separate site on 
CDKA/B subunits can induce activity of these subunits
Cell Cycle Checkpoint And Plant 
Growth Regulator 
 Cyclin A/B by Gibberellins. 
 D – type Cyclin by Cytokinin 
 Cdk inhibitor by Abscisic acid 

Auxin also increases the expression of CDKA;1 and mitotic 
cyclins, although application of exogenous auxin alone is 
not sufficient to induce cell division. 
Auxin and cytokinins are both necessary for 
progression through the G1-S and G2-M transitions as 
demonstrated in a variety of cultured plant cells. 
Cytokinin 
can also increase the expression and kinase activity of 
CDKA;1 by a mechanism involving removal of an inhibitory 
phosphate group on the kinase. 
In addition, CycD3;1 expression is also up-regulated by 
cytokinins. CycD3;1 appears to be a critical regulator of 
G1-S progression,
Cytokinin; 
Cytokinins Regulate Specific Components of the Cell Cycle 
Cytokinins regulate cell division by affecting the controls that 
govern the passage of the cell through the cell division cycle. 
Zeatin levels were found to peak in synchronized culture tobacco 
cells at the end of S phase, mitosis, and G1 phase.
Gibberellic acid (GA) generally promotes cell 
division, and during water submergence in 
deepwater rice GA has been shown to induce the 
expression of CycA1;1 and CDKB1;1 at the G1-S 
transition. This induction is followed by an 
increase in expression of mitotic B-type cyclins 
. 
Not all hormones promote progression through the 
cell cycle, however. The stress hormone abscisic 
acid (ABA) inhibits cell division under unfavorable 
environmental conditions. This may occur through 
up-regulation of expression of the cyclin kinase 
inhibitor ICK1 and down-regulation of expression 
and activity levels of CDKA;1.
Summary: Cell Cycle Control 
 A “clock” is running within the cell - of synthesis 
and degradation of cyclins - which activate cyclin-dependant 
kinases (Cdk’s), which activate other 
proteins to cause checkpoint transitions. 
 The “clock” is adjusted (cyclins and Cdk’s are 
regulated) by other proteins, based on: 
 External signals (growth factors) 
 Internal signals (correct completion of previous step)
REFERENCES 
 PLANT PHYSIOLOGY TAIZ AND ZEIGER 
 Miller CO, Skoog F, von Saltza MH, Strong F: Kinetin, 
a cell division factor from deoxyribonucleic acid. 
 Recent Developments in Plant Cell Cycle Research Professor Ahmad 
Shamsul Islam
Cell cycle regulation  ppt

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Cell cycle regulation ppt

  • 1.
  • 2.
  • 3. When a cell has grown to its maximum size it divides , and it take place a series of changes in a newly formed cell which involve in growth and division to form 2 daughter cells , it is called Cell cycle. It consist of two stages, A non dividing growing Interphase Or I Phase A Short Dividing Mitotic/ M Phase
  • 4.
  • 5.  The period between two mitotic divisions is called Interphase . It is further divisible into 3 stages: 1. • G1 phase 2. • S phase 3. • G2 phase
  • 6.
  • 7. G1 phase :  It is the post mitotic phase and takes place at the end of cell division the newly formed cells accumulate the energy and prepares themselves for the synthesis of DNA . During this , active synthesis of RNA and protein takes place . S phase :  It is the synthesis phase during this phase duplication of DNA and centriole takes places. The duplication of DNA results in the duplication of chromosomes . G2 phase :  It is the pre- mitotic gap phase (invisible phase) the synthesis of RNA and protein continues in this phase. The formation of macro molecules for spindle formation takes place and the cell prepare it self to go into the mitotic phase .
  • 8. MITOTIC PHASE M Phase follows the interphase. This last for a shot period compare to interphase .During this phase two important processes occur simultaneously they are karyokinesis (division of nucleus) : It results in the separation of chromosomes into two equal groups . Cytokinesis (division of cytoplasm) : It results in division of cytoplasmic components into approximately two halves. After M phase a cell may either enter interphase to repeat the cell cycle or G0 phase to arrest the cell cycle. The cells in G0 phase may grow in size and get differentiated .
  • 9. A checkpoint in the cell cycle is a critical control point where stop and go signals regulate the cycle. 3 major checkpoints are found in the G1, G2, and M phases.
  • 10. Regulation of the Cell Cycle: Cell Cycle Checkpoints
  • 11. G2 Checkpoint Control by MPF  Active MPF = Mitotic Cdk + mitotic cyclin  Cdk is cyclin-dependant kinase  MPF controls G2  M by phosphorylating and activating proteins involving in: Chromosome condensation Nuclear envelope breakdown Spindle assembly It’s own self-destruction
  • 13. G1 checkpoint • Controlled by G1 Cdks-cyclin • G1 cyclin levels also vary with the cell cycle • Many additional levels of phosphorylation, dephosphorylation regulate.
  • 14. • The Cell Cycle Is Regulated by Protein Kinases. • The mechanism regulating the progression of cells through their division cycle is highly conserved in evolution, and plants have retained the basic components of this mechanism. • The key enzymes that control the transitions between the different states of the cell cycle, and the entry of nondividing cells into the cell cycle, are the cyclin-dependent protein kinases, or CDKs
  • 15.  Cell division is a vital process that requires orderly progression .  Endogenous hormones such as auxin,cytokinins, abscisic acid, gibberellins and brassinosteroids as well as environmental factors all regulate progression through the cell cycle.  cell cycle events take place with clock-like precision . Recent studies have demonstrated that cell cycles in plants and animals are regulated by similar mechanisms.  A group of highly conserved serine/threonine kinases called cyclin-dependent kinases(CDKs) has been found to play a key role in guiding the cell cycle process.
  • 16. Four classes of cyclins : 1. G1-cyclins — help to promote passage through “ Start” or the restriction point in late G1 2. G1/S-cyclins — bind Cdks at the end of G1 and commit the cell to DNA replication 3. S-cyclins – binds Cdks during S phase and are required for the initiation of DNA replication 4. M-cyclins — promote the events of mitosis
  • 17. • Protein kinases are enzymes that phosphorylate proteins using ATP. • The regulated activity of CDKs is essential for the transitions from G1 to S and from G2 to M, and for the entry of nondividing cells into the cell cycle. • The transition from G1 to S requires a set of cyclins ( G1 cyclins) different from those required in the transition from G2 to mitosis, where mitotic cyclins activate the CDKs . • CDKs possess two tyrosine phosphorylation sites: One causes activation of the enzyme; the other causes inactivation. • Specific kinases carry out both the stimulatory and the inhibitory phosphorylation
  • 18. • Similarly, protein phosphatases can remove phosphate from CDKs, either stimulating or inhibiting their activity, depending on the position of the phosphate. • The addition or removal of phosphate groups from CDKs is highly regulated and an important mechanism for the control of cell cycle progression . • Cyclin inhibitors play an important role in regulating the cell cycle in animals, and probably in plants as well, although little is known about plant cyclin inhibitors.
  • 19. CDK activity can be regulated in various ways, but two of the most important mechanisms are (1) cyclin synthesis and destruction and (2) the phosphorylation and dephosphorylation of key amino acid residues within the CDK protein.
  • 20. • CDKs are inactive unless they are associated with a cyclin. Most cyclins turn over rapidly. • They are synthesized and then actively degraded (using ATP) at specific points in the cell cycle. • Cyclins are degraded in the cytosol by a large proteolytic complex called the proteasome. • Before being degraded by the proteasome, the cyclins are marked for destruction by the attachment of a small protein called ubiquitin, a process that requires ATP.
  • 21.  G2-M transition is also a major control point. Both A-type and B-type CDKs are thought to be involved in this process.  A-type CDKs are expressed constitutively, while the plant-specific B-type CDKs increase expression during the G2-M transition point.  CDKA and CDKB subunits interact with their respective cyclin partners (CycA/B).  Both the expression of CDKA/B and CycA/B genes and the activity of CDKA/B kinases are affected by plant hormones.  Auxin, GA and cytokinin increase expression of these genes, and cytokinin can also induce removal of an inhibitory phosphate group (T14/Y15) on CDKA/B subunits.  In an additional level of control, phosphorylation at a separate site on CDKA/B subunits can induce activity of these subunits
  • 22. Cell Cycle Checkpoint And Plant Growth Regulator  Cyclin A/B by Gibberellins.  D – type Cyclin by Cytokinin  Cdk inhibitor by Abscisic acid 
  • 23. Auxin also increases the expression of CDKA;1 and mitotic cyclins, although application of exogenous auxin alone is not sufficient to induce cell division. Auxin and cytokinins are both necessary for progression through the G1-S and G2-M transitions as demonstrated in a variety of cultured plant cells. Cytokinin can also increase the expression and kinase activity of CDKA;1 by a mechanism involving removal of an inhibitory phosphate group on the kinase. In addition, CycD3;1 expression is also up-regulated by cytokinins. CycD3;1 appears to be a critical regulator of G1-S progression,
  • 24. Cytokinin; Cytokinins Regulate Specific Components of the Cell Cycle Cytokinins regulate cell division by affecting the controls that govern the passage of the cell through the cell division cycle. Zeatin levels were found to peak in synchronized culture tobacco cells at the end of S phase, mitosis, and G1 phase.
  • 25. Gibberellic acid (GA) generally promotes cell division, and during water submergence in deepwater rice GA has been shown to induce the expression of CycA1;1 and CDKB1;1 at the G1-S transition. This induction is followed by an increase in expression of mitotic B-type cyclins . Not all hormones promote progression through the cell cycle, however. The stress hormone abscisic acid (ABA) inhibits cell division under unfavorable environmental conditions. This may occur through up-regulation of expression of the cyclin kinase inhibitor ICK1 and down-regulation of expression and activity levels of CDKA;1.
  • 26. Summary: Cell Cycle Control  A “clock” is running within the cell - of synthesis and degradation of cyclins - which activate cyclin-dependant kinases (Cdk’s), which activate other proteins to cause checkpoint transitions.  The “clock” is adjusted (cyclins and Cdk’s are regulated) by other proteins, based on:  External signals (growth factors)  Internal signals (correct completion of previous step)
  • 27. REFERENCES  PLANT PHYSIOLOGY TAIZ AND ZEIGER  Miller CO, Skoog F, von Saltza MH, Strong F: Kinetin, a cell division factor from deoxyribonucleic acid.  Recent Developments in Plant Cell Cycle Research Professor Ahmad Shamsul Islam