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tumor suppressor Gene
Action of pRB and p53
1
By
KAUSHAL KUMAR SAHU
Assistant Professor (Ad Hoc)
Department of Biotechnology
Govt. Digvijay Autonomous P. G. College
Raj-Nandgaon ( C. G. )
CONTENTS
• Introduction
• History
• Tumor suppressor gene- pRB
- RB gene
- Role of RB in regulation of cell cycle
- Tumor associated with RB gene mutation
• Tumor suppressor gene- p53
- What is p53 gene?
- Function of p53 gene
- How it regulates cell cycle
- What happen if p53 gene inactivated
- Cancer associated with p53 mutation
- Conclusion
- References
2
INTRODUCTION
Tumor suppressor proteins –
Tumor suppressor gene act as a cell
brakes; they encode proteins that restrain cell growth
and prevent cells from becoming malignant.
Oncogenes –
Encoded proteins that promote the loss of growth
control and the conversion of cell to a malignant
state.
3
Fig- (a) Mutated tumor suppressor gene (b) Oncogenes
4
HISTORY
• The existence of such genes originally came to light
from studies in the late 1960s.
• When normal and malignant rodent cells were fused
to one another. Some of the cell hybrids formed
from this type of fusion lost their malignant
characteristics, suggesting that a normal cell
possesses factors that can suppress the
uncontrolled growth of a cancer cell.
5
Tumor suppressor gene - pRB
• Tumor suppressor protein is a product of tumor
suppressor gene.
• It regulate cell growth by applying brake to cell
proliferation (Growth inhibition).
• Failure to growth inhibition cause carcinogenesis.
• And loss of function of this pRB gene is a key
events in carcinogenesis.
6
Loss Of Heterozygosity –
• Both normal alleles of normal function of
tumor suppressor gene tumor suppressor
gene.
• One allele active normal function of
(normal) and another tumor suppressor
abnormal (inactive) gene.
(Heterozygous state)
• Both are abnormal loss of function of tumor
(inactive) suppressor gene.
(loss of heterozygosity ) cause mutation
7
8
RB gene
• 1st discovered tumor suppressor gene.
• RB stand for Retinoblastoma.
• Retinoblastoma is a human childhood disease,
involving a tumor of retina.
• It occur both as a heritable trait and sporadically.
• It is often associated with deletion of band q14 of
chromosome 13.
• Retinoblastoma arises when both copies of RB gene
are inactivated.
9
Fig- (a) Sporadic case (b) Inherited case 10
Role of RB in regulation of cell
cycle
• The protein encoded by the RB gene, pRB, helps
regulate the passage of cells from the G1 stage of
the cell cycle into S phase.
• From G1 to S is a time of commitment for the cell;
once a cell enters S phase, it invariably proceeds
through the remainder of the cell cycle and into
mitosis.
• The transition from G1 to S is accompanied by the
activation of many different genes that encode
proteins ranging from DNA polymerases to cyclins
and histones.
11
• Among the transcription factors involved in
activating genes required for S phase activities are
members of the E2F family of transcription factors,
which are key targets of pRB.
• During G1, the unphosphorylated pRB is bound to
the E2F protein.
• The E2F–pRB complex binds to regulatory sites in
the promoter regions involved in cell cycle
progression, acting as a transcriptional repressor
that blocks gene expression.
• At the end of G1 Activation of the cyclin-dependent
kinase (Cdk) leads to the phosphorylation of pRB,
which can no longer bind the E2F protein.
12
• loss of the bound pRB converts the DNA-bound E2F
into a transcriptional activator, leading to expression
of the genes being regulated.
• The mRNA is translated into protein that are
required for the progression of cells from G1 into S
phase of the cell cycle.
NOTE-
• Some DNA tumor viruses (including adenoviruses,
human papilloma virus, and SV40) encode a protein
that binds to pRB, blocking its ability to bind to E2F.
13
Fig- Role of pRB in controlling transcription 14
Tumor associated with RB gene
mutation
• Retinoblastoma.
• Osteosarcoma.
• Breast cancer.
• Lung cancer.
15
Tumor suppressor gene - p53
• The most important tumor suppressor is p53 (named
for its molecular size) 53 kDa.
• It is located on band p13 of chromosome 17.
• Also called ‘’Guardian of the Genome’’.
• In 1990,p53 was recognized as the tumor-
suppressor gene.
• Its activity stop formation of tumor.
• Mutation in p53 is the cause of Li-Fraumeni
syndrome, which is rare form of inherited cancer.
• All normal cell have low level of p53.
16
Function of p53
• DNA repairing.
• Apoptosis.
• Regulation of cell cycle.
• Prevent neoplastic transformation either by
cell cycle arrest or by triggering apoptosis.
17
DNA damage
Trigger the expression of p53
Increase level of p53
Prevent cell from entering to S phase
It mean arrest of cell cycle at G1 phase
And p53 induce DNA repair gene
DNA repair DNA not repair
Degrade p53 permanent arrest apoptosis
Cell cycle continue
18
Fig- DNA of cell become damage
19
How it regulates cell cycle
• Activated p53 encodes a protein called p21 that
inhibits the cyclin-dependent kinase that normally
drives a cell through the G1 checkpoint.
• As the level of p53 rises in the damaged G1 cell,
expression of the p21 gene is activated, and
progression through the cell cycle is arrested.
• This gives the cell time to repair the genetic damage
before it initiates DNA replication.
20
• Cell cycle arrest is not the only way that p53
protects an organism from developing cancer.
• Alternatively, p53 can direct a genetically damaged
cell along a pathway that leads to death by
apoptosis.
• Including the activation of expression of the BAX
gene, whose encoded product (Bax) initiates
apoptosis.
21
Fig- p53 activity on damage DNA 22
What happen if p53 gene
inactivated
If both copies of the p53 gene are inactivated.
23
Cancer associated with p53
mutation
• Liver cancer.
• Lung cancer.
• Breast cancer.
• Ovarian cancer.
24
CONCLUSION
So, pRB and p53 tumor suppressor gene
are very important to inhibit the growth of
tumor or called malignant cancer.
25
REFERENCES
26

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tumor suppressor gene, prb, p53 gene

  • 1. tumor suppressor Gene Action of pRB and p53 1 By KAUSHAL KUMAR SAHU Assistant Professor (Ad Hoc) Department of Biotechnology Govt. Digvijay Autonomous P. G. College Raj-Nandgaon ( C. G. )
  • 2. CONTENTS • Introduction • History • Tumor suppressor gene- pRB - RB gene - Role of RB in regulation of cell cycle - Tumor associated with RB gene mutation • Tumor suppressor gene- p53 - What is p53 gene? - Function of p53 gene - How it regulates cell cycle - What happen if p53 gene inactivated - Cancer associated with p53 mutation - Conclusion - References 2
  • 3. INTRODUCTION Tumor suppressor proteins – Tumor suppressor gene act as a cell brakes; they encode proteins that restrain cell growth and prevent cells from becoming malignant. Oncogenes – Encoded proteins that promote the loss of growth control and the conversion of cell to a malignant state. 3
  • 4. Fig- (a) Mutated tumor suppressor gene (b) Oncogenes 4
  • 5. HISTORY • The existence of such genes originally came to light from studies in the late 1960s. • When normal and malignant rodent cells were fused to one another. Some of the cell hybrids formed from this type of fusion lost their malignant characteristics, suggesting that a normal cell possesses factors that can suppress the uncontrolled growth of a cancer cell. 5
  • 6. Tumor suppressor gene - pRB • Tumor suppressor protein is a product of tumor suppressor gene. • It regulate cell growth by applying brake to cell proliferation (Growth inhibition). • Failure to growth inhibition cause carcinogenesis. • And loss of function of this pRB gene is a key events in carcinogenesis. 6
  • 7. Loss Of Heterozygosity – • Both normal alleles of normal function of tumor suppressor gene tumor suppressor gene. • One allele active normal function of (normal) and another tumor suppressor abnormal (inactive) gene. (Heterozygous state) • Both are abnormal loss of function of tumor (inactive) suppressor gene. (loss of heterozygosity ) cause mutation 7
  • 8. 8
  • 9. RB gene • 1st discovered tumor suppressor gene. • RB stand for Retinoblastoma. • Retinoblastoma is a human childhood disease, involving a tumor of retina. • It occur both as a heritable trait and sporadically. • It is often associated with deletion of band q14 of chromosome 13. • Retinoblastoma arises when both copies of RB gene are inactivated. 9
  • 10. Fig- (a) Sporadic case (b) Inherited case 10
  • 11. Role of RB in regulation of cell cycle • The protein encoded by the RB gene, pRB, helps regulate the passage of cells from the G1 stage of the cell cycle into S phase. • From G1 to S is a time of commitment for the cell; once a cell enters S phase, it invariably proceeds through the remainder of the cell cycle and into mitosis. • The transition from G1 to S is accompanied by the activation of many different genes that encode proteins ranging from DNA polymerases to cyclins and histones. 11
  • 12. • Among the transcription factors involved in activating genes required for S phase activities are members of the E2F family of transcription factors, which are key targets of pRB. • During G1, the unphosphorylated pRB is bound to the E2F protein. • The E2F–pRB complex binds to regulatory sites in the promoter regions involved in cell cycle progression, acting as a transcriptional repressor that blocks gene expression. • At the end of G1 Activation of the cyclin-dependent kinase (Cdk) leads to the phosphorylation of pRB, which can no longer bind the E2F protein. 12
  • 13. • loss of the bound pRB converts the DNA-bound E2F into a transcriptional activator, leading to expression of the genes being regulated. • The mRNA is translated into protein that are required for the progression of cells from G1 into S phase of the cell cycle. NOTE- • Some DNA tumor viruses (including adenoviruses, human papilloma virus, and SV40) encode a protein that binds to pRB, blocking its ability to bind to E2F. 13
  • 14. Fig- Role of pRB in controlling transcription 14
  • 15. Tumor associated with RB gene mutation • Retinoblastoma. • Osteosarcoma. • Breast cancer. • Lung cancer. 15
  • 16. Tumor suppressor gene - p53 • The most important tumor suppressor is p53 (named for its molecular size) 53 kDa. • It is located on band p13 of chromosome 17. • Also called ‘’Guardian of the Genome’’. • In 1990,p53 was recognized as the tumor- suppressor gene. • Its activity stop formation of tumor. • Mutation in p53 is the cause of Li-Fraumeni syndrome, which is rare form of inherited cancer. • All normal cell have low level of p53. 16
  • 17. Function of p53 • DNA repairing. • Apoptosis. • Regulation of cell cycle. • Prevent neoplastic transformation either by cell cycle arrest or by triggering apoptosis. 17
  • 18. DNA damage Trigger the expression of p53 Increase level of p53 Prevent cell from entering to S phase It mean arrest of cell cycle at G1 phase And p53 induce DNA repair gene DNA repair DNA not repair Degrade p53 permanent arrest apoptosis Cell cycle continue 18
  • 19. Fig- DNA of cell become damage 19
  • 20. How it regulates cell cycle • Activated p53 encodes a protein called p21 that inhibits the cyclin-dependent kinase that normally drives a cell through the G1 checkpoint. • As the level of p53 rises in the damaged G1 cell, expression of the p21 gene is activated, and progression through the cell cycle is arrested. • This gives the cell time to repair the genetic damage before it initiates DNA replication. 20
  • 21. • Cell cycle arrest is not the only way that p53 protects an organism from developing cancer. • Alternatively, p53 can direct a genetically damaged cell along a pathway that leads to death by apoptosis. • Including the activation of expression of the BAX gene, whose encoded product (Bax) initiates apoptosis. 21
  • 22. Fig- p53 activity on damage DNA 22
  • 23. What happen if p53 gene inactivated If both copies of the p53 gene are inactivated. 23
  • 24. Cancer associated with p53 mutation • Liver cancer. • Lung cancer. • Breast cancer. • Ovarian cancer. 24
  • 25. CONCLUSION So, pRB and p53 tumor suppressor gene are very important to inhibit the growth of tumor or called malignant cancer. 25