D2.1 Cytoplasm and Nuclear division

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54 Terms

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Cytokinesis in animal cells

The final stage of cell division when the membrane folds inwards and a ring of actin and myosin contracts and pinches membrane together

  • This is the division of the cytoplasm

  • Forms a cleavage furrow - occurs when an animal cell membrane folds inwards

  • Actin and myosin for a contractile ring → the membrane pinches off to form 2 cells

  • Organelles are distributed between both ends of the cell so organelles in both cells are formed

  • Mitochondria (and chloroplasts in plant cells) must move to each side as the new cell cannot synthesise these

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Cytokinesis in plant cells

  • Vesicles fuse together to form a plasma membrane and cell wall

  • Golgi vesicles containing carbohydrates collect along the centre of the cell to form a cell plate

  • Plant cells cannot form a cleavage furrow due to the presence of a cell wall

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Oogenesis - unequal division of cytoplasm

  • This is the formation of eggs in ovaries

  • Primary oocytes divide to form secondary oocytes + a smaller polar body

  • This occurs before fertilisation

  • Secondary oocytes divides again to form an ovum and a second polar body

  • The final large ovum absorbs the cytoplasm + contents of polar bodies to form one large egg

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Budding

  • A method of sexual reproduction in some species

  • Swelling forms out the side (a bud)

  • The bud continues to grow and splits off

  • Nucleus copies by mitosis - one nucleus moves into the bud

  • Scar is left behind on the parent cell

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Mitosis + meiosis similarities

  • Both nuclear division

  • Nucleus must divide before cytokinesis or the cell will be anucleate

  • DNA replication is therefore a prerequisite for both

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Products + uses of mitosis

  • 2 genetically identical cells

  • Forms diploid cells

  • 1 division

  • Used for growth + to replace cells and for asexual reproduction

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Products + uses of meiosis

  • 4 genetically different cells

  • Forms haploid cells

  • 2 divisions

  • Used to make gametes

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Condensation of chromosomes

  • DNA is coiled around histone proteins

  • 8 histones + DNA = a nucleosome

  • Histone = positively charged so attracts negatively charged DNA

  • Supercoiling occurs - DNA further twists around nucleosomes to form tight coiled structure

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Movement via microtubules

  • Microtubules are a part of the cytoskeleton

  • They can lengthen and shorten via polymerisation and depolymerisation

  • Microtubule motors = also needed to move chromosomes to cell centre

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Mitosis: Prophase

  • Nuclear envelope + nucleolus breaks down

  • Genetic material now in cytoplasm

  • Chromosomes condense - supercoiling of DNA

  • Centrioles form at opposite poles

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Mitosis: Metaphase

  • Chromosomes are bound to spindle fibres at the centriole

  • Chromosomes line up at the equator of the cell

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Mitosis: Anaphase

Chromatids are pulled by the spindle fibre to opposite poles

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Mitosis: Telophase

  • Chromatids decondense

  • 2 nuclear membranes reform - 2 nuclei

  • spindle fibre breaks down

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Mitotic index

  • Used to calculate how regularly cells divide

  • Can determine whether cells are cancerous

  • Mitotic index = cells in mitosis/total number of cells

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Why mitosis is important

It is nuclear division, important for human life and needed for:

  • Growth/production of extra body cells

  • Development of an embryo

  • Wound healing/tissue repair/cell replacement

  • Clonal selection/division of lymphocytes for antibody production during immune response

  • First stage of gametogenesis (forming sperm and egg)

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Meiosis: Prophase 1

  • Nuclear membrane breaks down

  • Chromosomes condense

  • Chromosomes form ‘homologous pairs’ called bivalents

  • Crossing over may occur

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Meiosis: Metaphase 1

  • Homologous pairs line up at equator

  • Spindle fibres connect

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Meiosis: Anaphase 1

  • Spindle fibres contract + shorten

  • Homologous chromosomes are pulled to opposite poles

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Meiosis: Telophase 1

  • Chromosomes decondense

  • Nuclear membrane reforms

  • 2 haploid cells are formed

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Meiosis: Prophase 2

  • Nucleolus and nuclear membrane breaks down

  • Chromosomes condense

  • Spindle fibres form perpendicular to prophase 1 and attach to a single chromosome

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Meiosis: Metaphase 2

Chromosomes line up at the equator of thecell

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Meiosis: Anaphase 2

  • Chromatids are moved to opposite poles

  • Occurs due to spindle fibred condensing and shortening

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Meiosis: Telophase 2

  • Chromosomes decondense

  • Nuclear membrane reforms

  • 4, genetically different haploid cells are produced

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Haploid definition

A cell containing a single set of chromosomes

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Crossing over (recombination)

  • A cause of variation during meiosis

  • Occurs during prophase 1

  • When homologous chromosomes are paired up, non-sister chromatids come into contact with each other

  • Contact point is called the chiasma

  • An enzyme cuts and swaps the chromosomes

  • This creates a new combination of alleles and forms recombinant chromatids

  • Recombinant chromatids = chromatid that has information crossed over, a combination of both chromatids DNA

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Independent assortment (random orientation of bivalents)

  • Causes variation during meiosis

  • The arrangement of chromosome combinations during metaphase 1 lead to different chromosome combinations

  • This means different combinations of chromosomes are pulled to opposite ends of the cell

  • Can also occur for chromatids during metaphase 2, although only relevant if crossing over has occurred

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Random fusion of gametes

  • Causes variation

  • Which sperm fertilised the egg is random, creating variation

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Non-disjunction

  • Occurs when there is a mistake in meiosis

  • Happens if chromosomes in anaphase 1 or chromatids in anaphase 2 fail to separate

  • This can cause gametes to have an incorrect number of chromosomes

  • Down syndrome occurs when there is an extra chromosome - 2 copies of chromosome 21

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Factors affecting non-disjunctions

  • Chances of non-disjunction increases as parental age increases

  • Particularly strong correlation between maternal age and occurrence of non-disjunction

  • Risk of chromosomal abnormalities in offspring increase significantly after the age of 30

  • There is a higher risk of of chromosomal errors in offspring as a result of non-disjunction in meiosis 1

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Cell proliferation and meristems

  • Cell proliferation is the increase in the number of cells, caused by cell growth and cell division

  • Meristem cells - retain the ability to divide by mitosis to form new cells/tissues

  • Apical meristem cells - cause lengthening and upwards growth, occur at tips of shoots and roots

  • Lateral meristem cells - located at the cambium, causes the stem to grow wider

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Cell proliferation in embryos

  • Number of cells in the embryo doubles with each division

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Cell proliferation - replacement in wound healing

  • Dermal cells divide - make more cells

  • new cells migrate upwards towards the skin surface

  • Dead cells on the surface are replaced and fall off

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Cell replacement - wound healing

  • Clotting occurs - fibrin matrix + platelets form a clot

  • During proliferation, stem cells are activated in the dermal layer. These regenerate new cells to repair the wound

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The phases of interphase

Consists of gap phases (G1 and G2) and a synthesis phase (S) in between

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Interphase: G1

  • Cellular contents (excluding chromosomes) are duplicated

  • Protein synthesis occurs

  • Cell doubles in size

  • Cytoplasm volume is increased

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Interphase: S

All 46 chromosomes are duplicated

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Interphase: G2

  • The cell proofreads the duplicated chromosomes, making necessary repairs

  • Microtubules are synthesized

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What the G1 checkpoint checks for

  • Cell size

  • DNA damage

  • Growth factors

  • Nutrients

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What the G2 checkpoint checks for

  • Cell size

  • DNA replication

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What the spindle assembly checkpoint checks for

Chromosome attachment to the spindle

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The importance of checkpoints during the cell cycle

  • Important to ensure the cell only divides when it has grown to the right size, DNA is error free and chromosomes in the correct positions

  • To ensure this, checkpoints in the cell cycle act as control mechanisms

  • The cell cannot proceed to next cell cycle stage unless they have completed the previous one

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The roll of cyclins

  • Cyclins are chemicals that control the cell cycle

  • There are 4: D, E, A and B

  • Their levels rise and fall throughout the cell cycle - determines what stage the cell cycle is in

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Each cyclin and their roll

D - Triggers the cell to move from G0 to G1 and from G1 to S phase

E - Prepares the cell for DNA replication in S phase

A - activates DNA replication inside the nucleus in S phase

B - Promotes the assembly of the mitotic spindle and other tasks in the cytoplasm to prepare for mitosis

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Cyclins and kinase enzymes

  • Each cyclin activates a different cyclin dependent kinase enzyme (CDK)

  • The CDK then activates a target protein, regulating the cell cycle

  • The cyclins are then destroyed

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Mitosis promoting factors

  • A complex between cyclin B and an associated CDK

  • This triggers condensation of DNA, spindle formation, nuclear membrane breakdown e.t.c

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Serendipity

  • A happy and unexpected discovery made by accident

  • Discovery of cyclins by Tim Hunt is an example of serendipity in science

  • He was awarded the physiology nobel prize in 2001 for this

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Cancer

  • Uncontrolled cell division that causes tumour formation

  • May occur if cells divide at a faster rate than are destroyed

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Cancerous vs normal cells

Cancer:

  • Large, variable shaped nuclei

  • small cytoplasmic volume

  • Variation in cell size and shape

  • Disorganised arrangement

  • Larger levels of dividing cells

Normal:

  • small, uniform nuclei

  • Large cytoplasmic volume

  • Conformity in cell size and tissue

  • Cells arranged in discrete tissues

  • Lower levels of dividing cells

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Primary and secondary cancer

  • A mutation causes rapid cell division

  • Results in a group of rapidly dividing cells called a primary tumour

  • Vascularisation occurs - blood vessels divert towards the tumour and surround it

  • One cancerous cell may detach, enter blood and go to a different organ

  • This causes the formation of a new, secondary tumour elsewhere in the body

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Benign vs malignant tumours

Benign tumours = non cancerous, cannot spread to other parts of the body

Malignant tumour = cancerous tumour that may spread to other sides via the blood stream and lymphatic system

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Metastasis

  • Can occur in primary tumours

  • Is the process when cells break away and secondary tumours form in other areas

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Cancer and oncogenes

  • Proto-oncogene and tumour repressor gene control cell division

  • Proto-oncogene stimulates cell division, tumour suppressor gene slows it down

  • If these occur at the same rate, normal cell division occurs

  • If a proto-oncogene mutates to form an oncogene - there will be uncontrolled cell division and cancer

  • If the tumour suppressor gene is inactivated, there will be uncontrolled cell division and cancer

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Mutagens

  • An agent, such as radiation or a chemical, that causes a mutation

  • The chance of one mutation causing cancer is small

  • As there are many cells in the body, the total chance of tumour formation is higher over a lifetime

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Cigarettes → cancer

  • There is a strong correlation between cigarettes and cancer

  • Cancer is a global problem