Cell cycle & Mitiosis Flashcards

1
Q

Why is cell division is important ?

A
  • important in growth and repair of tissues in multicellular organism
  • reproduction of all organisms
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2
Q

What four events must occur for cell division ?

A
  • a reproductive(intra/extracellular) signal initiates cell division
  • replication of DNA
  • Segregation :Distribution of DNA into 2 new cells
  • Cytokinesis: separation of cellular material into 2 new cells
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3
Q

How does binary fission occur ?

A
  • Replication occurs as the DNA is threaded through ‘ Replication complex’ of proteins
    -Rapidly dividing prokaryotes the entire time is DNA replication between cell divisions
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4
Q

Binary fission how 2?

A

When replication is complete the daughter DNA molecules are segregated at opposite ends
The ORI regions move towards opposite ends of cells aided by special protein

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5
Q

3 binary fission ?

A

Cytokinesis begins by a pinching in of a plasma membrane ; protein fibres (mostly Ftsz) form ring
New Cell wall materials are synthesised resulting in a separation of 2 cells being formed

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6
Q

Cell cycle in eukaryotes consist of ?

A

MITOSIS
CYTOKINESIS
INTERPHASE

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7
Q

Interphase ?

A

nucleus is visible & cell functions,including DNA replication,occur
Begins after cytokinesis ends when mitosis starts

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8
Q

Interphase subspaces ?

A

G1: (Gap 1) between cytokineses and S phase ;chromosomes are single , unreplicated structures
- Duration varies from minutes to years
Some cells enter resting phase (G0)

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9
Q

Interphases 2 nd sub stage ?

A

G1 TO S transition the commitment is made to DNA replication and subsequent cell division .
Called Restriction (R )point

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10
Q

Describe S phase & G2 Phase ?

A

S phase -(synthesis ) DNA replicates forming 2 sister chromatids stay together
G2 :(gap 2 ) cell prepares for mitosis
By synthesising structures to move the chromatids

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11
Q

How do transitions occur from 1 stage to the next ?

A

Specific signals trigger this-add more

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12
Q

What do these signals act through ?

A

through proteins called cyclin-dependant kinases (Cdk’s)
Kinase catalyse transfer of a phosphate group from ATP to a protein (Phosphorylation)
A Cdk must be activated by binding to a cyclin protein
Allosteric regulation altering the shape of Cdk thus exposing its active site to allow it to transfer a phosphate

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13
Q

Is there 1 cyclin-CD-R complex ?

A

no there ar many. At diff stages
1.) G2 PHASE
2.) MITOSIS
3.)G1
4.) S PHASE

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14
Q

What does the Cyclin Cdk do at the G1-S transition ?

A

Progress between the restriction point depends on Retinoblastoma protein (RB)
RB usually inhibits cell cycle BUT when phosphorylated by cyclin Cdk in a lot of places ,RB becomes inactive (changing 3D structure) and thus allows cell cycle

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15
Q

What are cell cycle checkpoints ?

A

G1- DNA damage
S - incomplete replication or DNA damage
G2 - DNA damage
M - chromosomes unattached to spindle

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16
Q

Mitosis

A

Newly replicated chromosomes-SISTER CHROMATIDS
-separates into 2 new nuclei
Sepeerating many large liner chromosomes would be diffifvutl

17
Q

How is DNA packed ?

A

Eukaryotic DNA molecule are “packed” and organised by histone proteins even uncondensed DNA is wound around histones to form nucleosomes.
When the chromosomes condense these Hilton’s begin to pack together

18
Q

The phases of mitosis ?
PROPHASE

A

The chromatin condenses and distinct chromatids become visible under a microscope

19
Q

PROMETAPHASE?

A

Nucleus envelope breaks down and chromosomes attach to the ‘spindle ‘ of microtubles

20
Q

ANAPHASE

A

The chromatids seperate and move to opposite poles by the spindle

21
Q

TELOPHASE

A

Nuclear envelope reforms,spindle disappears,chromosomes become less compact

22
Q

Interphase

A
  • Orientation is determined but the centrosome an organelle near the nucleus
23
Q

Prophase in depth

A

Each centrosome can consist of 2 centrioles- hollow tubes formed by microtubules at right angles

The centrosome doubles during S phase ;during prophase they move to oppposite ends of the nuclear envelope

24
Q

PROMETAPHASE

A

Late in prophase ,the spindle attachment points called kinetochores develop on each chromatid

Microtubules form between the poles and the chromosomes to make up the spindle fibres
Nuclear envelope breaks down and chromosome attach to a spindle of microtubule

25
Q

METAPHASE

A

2 types of microtubules in the spindle
Chromosomes line up in the middle of/ equatorial plate

  • polar microtubules form spindle framework; run from one pole to the other
  • Kinetochore microtubules attach to kinetochores on the sister chromatids and to microtubules in opposite halves of the spindle
26
Q

ANAPHASE

A

After separation ,the chromatids are called daughter chromosomes

  • chromatids share a centromere
  • chromosomes have their own centromere
    During the separation of SC -controlled by M phase Cyclin-Cdk; it activates ANAPAHSE -PROMOTING COMPLEX(APC)

Cohesion that hold the chromatids together is hydrolysed by seperase.
Chromatids separate and move to opposite poles of spindle

27
Q

Anaphase 2

A

Kinetochores have motor proteins; energy from ATP moves chromosomes along the microtubules

Kinetochores microtubules also shorten ,drawing chromosomes towards pole

28
Q

Telophase

A

Nuclear envelope reforms spindle fibres disappear chromosomes become less compact

29
Q

Cytokineses

A

Division of the cytoplasm follows mitosis
In animal cells the plasma membrane pinches in between the nuclei
\

30
Q

Cytokinesis in plant cells

A

The membrane bound vesicles appear along the plane of cell division .
These fuse to form a new plasma membrane

Contents of vesicles form a cell plate -the beginnings of new cell wall.