Biol 1057 - Mitosis & Meosis Flashcards

1
Q

Outline where genetic information is stored

A

DNA

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2
Q

Briefly define genome

A
  • An organisms complete set of genes in a cell which usually doesn’t change
  • Human genome is 3,2 billion bases
  • Smallest genomes are found in simple unicellular species
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3
Q

Outline how many chromosomes we have and how we cope with it

A
  • 1 chromosome = 4cm
  • 46 chromosomes – this is approximately 1.84m of
    DNA in every cell of your body
  • DNA exists in a highly condensed state within the cell nucleus
    1000-fold more tightly packed than “naked” DNA
  • Achieved with the help of proteins, the majority called histones
  • DNA & Histones
    are collectively called
    “chromatin”
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4
Q

Define a chromosome

A
  • A chromatin segment carrying the genetic information
  • Chromosomes carry genes
  • Humans have 23 chromosomes pairs
  • Homologous chromosomes carry same genes
    but are not identical as nobody has two identical parents.
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5
Q

Define diploid

A
  • Organisms/cells have with two full sets of chromosomes, one from the mother and one from the father
    (2N), called homologous chromosomes
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6
Q

Outline the growth phase

A

Chromosomes and DNA packaging
- DNA complexed with histones to form nucleosomes which consists of 8 histone proteins around which DNA wraps
- Nucleosomes form beads on DNA string and nucleosomes fold to produce 30nm fiber which then forms loops
which are compressed and folded to produce wide fiber
- Tight coiling of 250nm fiber produces chromatid of a chromosome

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7
Q

Briefly outline how a chromosome works

A
  • Each chromosome contains two identical parts called “sister-chromatids”
  • Chromatids stay connected initially at the centromere
  • Every chromosome gives rise to two identical chromosomes.
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8
Q

Outline interphase stage as a stage of mitosis

A
  • Longest stage in cell cycle
  • cell carry on their usual functions (G1)
  • DNA & organelles duplicate in preparation for mitosis (S)
  • after DNA replication and before mitosis (G2)
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9
Q

Outline prophase

A
  • Chromosomes condense & become visible
  • Centrioles separate to move to opposite poles of the cell to form mitotic spindle fibres
  • Nuclear envelope & nucleolus break down
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10
Q

Outline prometaphase

A
  1. Centrosomes on opposite poles of the cell
  2. Each chromatid is attached to a spindle fiber
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11
Q

Outline metaphase

A
  • Sister chromatids line up along the equator of the cell
  • Spindle fibres released from poles attach to chromatids by centromere
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12
Q

Outline anaphase

A

STAGE REQUIRES ATP provided by respiration

- Centromere divides separating sister chromatids and become daughter chromosomes
- Spindle fibres contract and chromosomes (no longer chromatids) pulled to opposite poles

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12
Q

Outline telophase

A
  • Chromosomes at each pole decondense
  • Cytoplasm splits(CYTOKYNESIS) and nuclear envelopes form around each group of chromosomes
  • 2 daughter cells created which are genetically identical
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13
Q

Briefly describe meiosis

A

Meiosis produces male and female gametes
- Produces haploid gametes (N)
- In males, meiosis is a part of
spermatogenesis, which occurs in the
testes and produces sperm.
- In females, meiosis is a part of oogenesis,which occurs in the ovaries & produces
eggs/oocytes.
- Upon fertilization the zygote (2N) undergoes mitosis and develops to a fetus (unborn child)
- After birth mitosis continues throughout life
for growth and repair.

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14
Q

Outline 1 way of how genetic variation occurs

A

Prophase I - Synapsis
Homologous chromosomes
(containing two sister-chromatids
each) pair, line up side-by-side
gene-by-gene.

Homologous Recombination
- Non-sister chromatids exchange genetic material.
- Crossover is in average is slightly more than two per
homologous pair in humans.
Sister chromatids may no longer be identical and
instead may have different combinations of alleles.

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15
Q

Outline a 2nd way of how genetic variation occurs

A

Homologous pairs are oriented randomly
- - The number of possible arrangements is related to the chromosome number (x)
and for two homologous chromosomes is 2x
- In humans, with 23 pairs of homologs (M & F), each gamete contains one of
8,388,608 (2to the power of 23) possible chromosome combinations, all equally likely.
- 3 chromosome pairs, 23= 8 chromosome arrangement combinations, 4 shown here

16
Q

Outline the steps of meiosis 1

A
  • DNA replicates once but nucleus divides twice
    Prophase l
  • Tetrads form, and crossing-over occurs as chromosomes condense;
    the nuclear envelope fragments.
  • Metaphase I
    Tetrads align at the spindle equator. Elther homologue can face either pole.
  • Anaphase I
    Homologues separate, and dyads move to poles.
    Telophase I
  • Daughter nuclei are haplold, having received one duplicated chromosome from each homologous pair.
17
Q

Outline the steps of meiosis 2

A

Prophase l
Chromosomes condense, and the nuclear envelope fragments.
Metaphase ll
The dyads align at spindle equator
Anaphase ll
Sister chromatids separate, becoming daughter chromosomes that move to the poles, centromeres split
n =2
Telophase Il
Four haploid daughter cells are genetically different from each other and from the parent cell.

18
Q

Compare mitosis to meiosis

A

Mitosis happens in somatic
cells that build our bodies
Meiosis happens in germ cells
* specialized cells of different
origin to the somatic cells
* destined to undergo meiosis
and transfer genetic
information to off-springs.
* present in the testis or
ovaries.

19
Q

Outline haploid nuclei in males packed into sperm

A
  • Spermatogenesis initiates in germ cells called spermatogonia.
  • The entire process takes place in testis
  • The process from spermatogonium to sperm takes about 74 days.
20
Q

Outline haploid nuclei in femals packed into oocytes

A
  • Formation of the ovum (egg cell) is produced at the end of oogenesis in the
    ovaries of the females
  • Egg cells are massive in comparison to the sperm, as they need to support the
    growth of the new organism (e.g. proteins, organelles)
  • Only 1 out of 4 haploid cells will become an oocyte, which gets all the
    cytoplasmic content. The other 3 haploid cells will eventually become tiny
    polar bodies.
  • meiosis in females starts in about 5 months fetus, the process is paused at
    prophase I
  • only after puberty a selected number of cells can continue meiosis as part of
    the menstruation cycle
  • the large periods between initiation and completion of meiosis may lead to
    nondisjunction as females age.
21
Q

Outline how meiosis can go wrong

A
  • nondisjunction occurs when chromosomes fail to separate at either
    anaphase I or anaphase II
  • spindle fibers do not form properly or attach correctly to a
    chromosome
  • Result is sperm or egg cell more or less copies of a particular
    chromosome (aneuploidy)
22
Q

Outline polypoidy and aneuploidy

A
  • Females have two X
    chromosomes (XX)
  • males have one X and one Y
    chromosome (XY)
  • Polyploidy: when a cell has one
    or more complete sets of extra
    chromosomes
  • Aneuploidy: when a cell has
    one or just few extra or missing
    chromosomes e.g. trisomy,
    monosomy.
23
Q

Outline an autosomal trisomy

A

² Persons usually have three copies of chromosome 21
² The chances of a woman having such child increase rapidly with
age, starting at about age 40.
² facial features, a unique pattern of hand creases, short stature, fissured
tongue, a round head.
² Intelligence varies greatly: some children have profound mental impairment,
whereas others learn well.
² Many affected children die before their first birthdays, often because of
congenital heart defects.
² Above-average risk for leukemia and Alzheimer disease.