Cell cycle presentation by Salman Ul Islam.

REGULATION OF CELL CYCLE

SALMAN UL ISLAM, (MS),CELLULAR BIOCHEMISTRY LAB.

SALMAN UL ISLAM, (MS),CELLULAR BIOCHEMISTRY LAB.

2013298039

CONTENTS

Introduction Overview of the cell cycle Cell-cycle control system Summary

INTRODUCTION

“Where a cell arises, there must be a previous cell, just as animals can only arise from animals and plants from plants.

A cell reproduces by carrying out an orderly sequence of events in which it duplicates its contents and then divides in two.

This cycle of duplication and division, known as the cell cycle, is the essential mechanism by which all living things reproduce.

Cell Cycle Regulation

How is cell division and growth regulated?

Growth factors-- stimulate cell growth

Mitogens-- trigger cell division

Survival signals-- disable apoptotic mechanisms

OVERVIEW OF THE CELL CYCLE

The eucaryotic cell cycle is traditionally divided into four phases:

M phase: constituted by mitosis (nucleus division) and cytokinesis (cell splits in two). The period between one M phase and the next is called interphase. The interphase encompasses the remaining three phases of the cell cycle.

S phase ( S=synthesis): the cell replicates its nuclear DNA. S phase is flanked by two phases in which the cell continues to grow.

G 1 phase (G= gap): it is the interval between the completion of M phase and the beginning of S phase (DNA synthesis).

G2 phase: interval between the end of S phase and the beginning of M phase.

Essential Cell Biology (© Garland Science 2010)

CHECKPOINTS IN CELL-CYCLE REGULATION

Two important checkpoints occur in G1 and G2.

The G1 checkpoint allows the cell to confirm that the environment is favorable for cell proliferation and its DNA is intact before committing to S phase.

G2 checkpoint ensures that cells do not enter mitosis until damaged DNA is repaired and DNA replication is complete.

CELL-CYCLE CONTROL SYSTEM DEPENDS ON CYCLICALLY ACTIVATED PROTEIN KINASES

Key proteins are activated and then inactivated that regulate DNA replication, mitosis, and cytokinesis. Phosphorylation followed by dephosphorylation is one of the most common ways to switch the activity of proteins on and then off.

Protein kinases are activated at appropriate times in the cycle, after which they quickly become deactivated again.

Switching these kinases on and off is done by cyclins, so kinases are therefore known as cyclin-dependent protein kinases or Cdks.

CDKS ACTIVITY IS ALSO REGULATED BY PHOSPHORYLATION AND DEPHOSPHORYLATION

For M-Cdk to be maximally active, it has to phosphorylated at one or more sites by a specific protein kinase, and dephophorylated at other sites by specific protein phosphatase.

The removal of the inhibitory phosphate groups by the phosphatase is the final step that activates the M-Cdk at the end of interphase.

Then M-Cdk complex can activate more of the same complexes. This positive feedback produces the sudden, explosive increase in M-Cdk activity that drives the cell abruptly into M phase.

CDKS ARE REGULATED BY ACCUMULATION AND DESTRUCTION OF CYCLINS

Cyclin concentration plays an important part in timing the events of cell cycle.

M cyclin= cyclin that helps drive cells into M phase.

M-cyclin synthesis starts immediately after cell division and continues steadily throughout interphase. The cyclin concentrates, so that its concentration rises gradually and helps time the onset of mitosis; its rapid elimination then helps initiate the exit from mitosis.

CDKS ARE REGULATED BY ACCUMULATION AND

DESTRUCTION OF CYCLINS (CONT…)

As mitosis nears completion, multiple molecules of the protein ubiquitin are covalently attached to the M-cyclin by anaphase promoting complex (APC).

This ubiquitination marks the cyclin for degradation in proteosomes, large proteolytic machines found in all eucaryotic cells. Destruction of the cyclin inactivates the Cdk.

DIFFERENT CYCLIN-CDK COMPLEXES


Distinct Cdks associate withdifferent cyclins to trigger thedifferent events of the cellcycle.

S-PHASE CYCLIN-CDK COMPLEXES INITIATE DNA REPLICATION ONCE

PER CELL CYCLE

Initiates DNA replication and helps block Rereplication.

DNA replication begins at origins of replication. Origin recognition complex (ORC) remains bound

to the origin of replication; serves as a sort of landing for other regulatory proteins.

Cdc6 binds to ORC in G1, promotes additional proteins binding to form pre-replicative complex, making the replication origin ready to “fire”. S-Cdk then pulls the “trigger” initiating DNA replication.

S-Cdk helps phophorylate Cdc6, causing it and the other proteins in the pre-replicative complex to dissociate from the ORC after an origin has fired.

CELL CYCLE ARREST

The cell-cycle control system can arrest the cycle at specific checkpoints. The molecular mechanisms of these are poorly understood.

In some cases, however, Cdk inhibitor proteins come into play.

For example DNA damage causes increased concentration and activity of p53 (gene regulatory protein) which activates the transcription of a gene encoding a Cdk inhibitor protein called p21.

The p21 protein binds to G1/S-Cdk, preventing them from driving the cell into S phase.

CELLS CAN DISMANTLE THEIR CONTROL SYSTEM AND WITHDRAW FROM THE CELL

CYCLE

This is a different matter from pausing in the middle of a cycle.

In human body, e.g, nerve cells and skeletal muscle cells persist for a lifetime without dividing, they enter G0.

G0 is modified G1 state in which the cell-cycle control system is largely dismantled, in that many of the Cdks and cyclins disappear.

The G1 checkpoint is therefore sometimes called Start, passing it represents a commitment to complete a full dividion cycle.

•Cell type Cell cycle time•Early frog embryo cells ~30 minutes•Yeast cells 1.5–3 hours•Intestinal epithelial cells ~12 hours•cultured fibroblasts ~20 hours•Human liver cells ~1 year

Eucaryotic Cell-Cycle

Times

SUMMARY

The control system depends on a set of proteins kinases, each composed of Cyclin and Cdk.

The control system also depends on protein complexes such as APC.

The Cdks are cyclically activated by both cyclin binding and the phosphorylation of some amino acids and the dephosphorylation of others; when activated, Cdks phophorylate key proteins in the cell.

The cell cycle control system can halt the cycle at specific check points to ensure that the next step in the cycle does not begin before the previous one has finished, and intracellular and extracellular conditions are favorable.

Cell cycle presentation by Salman Ul Islam.

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Transcript of Cell cycle presentation by Salman Ul Islam.