3.3 Meiosis Flashcards

1
Q

Meiosis is a ___________ of the nucleus to form _____________.

A

reduction division, haploid gametes

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2
Q

Meiosis I overview

A
  • Diploid nucleus (2n) 🡪 haploid nucleus (n)
  • Homologous chromosomes separate
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3
Q

Meiosis II overview

A
  • Haploid nucleus (n) 🡪 haploid nucleus (n)
  • Sister chromatids separate
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4
Q

Product of meiosis

A

4 haploid (n) daughter cells

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5
Q

Meiosis occurs in

A

GONADS (testes or ovaries)
SPERMATOGENESIS - creates sperm cells
OOGENESIS - creates egg cells

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6
Q

To compensate for the chromosome doubling during fertilisation gametes undergo …

A

meiosis, which halves the chromosomes present in gametes compared to the parent

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7
Q

Sexual reproduction involves ….

A

fertilisation, the fusion of gametes (sex cells), one from each parent.

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8
Q

Interphase

A

In the S-phase of the interphase before meiosis begins, DNA replication takes place.

Chromosomes are replicated and these copies are attached to each other at the centromere.

The attached chromosome and its copy are known as sister chromatids.

Following S-phase, further growth and preparation take place for meiosis.

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9
Q

Prophase I

A

DNA supercoils and chromosomes condense

Nuclear membrane dissolves

Centrioles migrate to the poles of the cell

The homologous chromosomes associate with each other to form bivalents (synapsis)

Chiasma = point of contact between the two non-homologous sister chromatids

Crossing-over between non-sister chromatids can take place. This results in recombination of alleles and is a source of genetic variation in gametes.

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10
Q

Metaphase I

A

The bivalents line up at the equator.

Random orientation occurs - each bivalent aligns independently and hence the daughter nuclei get a different mix of chromosomes.

This is a significant source of genetic variation

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11
Q

Anaphase I

A
  • Spindle fibres contract.
  • Homologous pairs pulled apart (separate)
  • This is the reduction division – the bivalent is split and half the chromosomes move towards each pole.
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12
Q

Telophase I

A

The nuclei are now haploid (N) not diploid (2N): they each contain one pair of sister chromatids for each of the species’ chromosomes.

The cytoplasm begins to divide by cytokinesis.

New nuclei form

Chromosomes decondense

n.b. If crossing-over and recombination has occurred then the sister chromatids will not be exact copies.

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13
Q

Prophase II

A

Nuclear membranes dissolves

Chromosomes, consisting of two sister chromatids, condense

No crossing-over occurs

Centrioles move to opposite poles

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14
Q

Metaphase II

A

Spindle fibres form and attach at the centromeres.

Pairs of sister chromatids align at the equator.

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15
Q

Anaphase II

A

The sister chromatids are separated. The chromatids (now called chromosomes are pulled to opposite poles.

Spindle fibres contract and the centromeres are split.

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16
Q

Telophase II

A

Nuclear membrane reforms

Chromosomes decondense

Cytokinesis begins, dividing the cells.

The end result of meiosis is four haploid gamete cells.

Fertilisation of these haploid gametes will produce a diploid zygote.

17
Q

Crossing-over between non-sister chromatids results in…

A

recombination of alleles

18
Q

Random orientation of the homologous chromosomes means…

A

there are 2n possible orientations in metaphase I. That is 223 in humans – or 8,388,068 different combinations in gametes!

19
Q

Because both crossing-over and random orientation occur during meiosis the result is…

A

effectively infinite genetic variation in the haploid gamete.

20
Q

mitosis vs meisis

A
  • mitosis
    One division
    Diploid cells produced
    No crossing-over in prophase
    No chiasmata formation
    Homologous pairs do not associate and line up at the equator in metaphase
    Sister chromatids separate in anaphase
  • meiosis
    Two divisions
    Haploid gametes produced
    Crossing-over in prophase I
    Chiasmata form
    Homologous pairs associate as bivalents and lined up at the equator in metaphase I
    Homologous pairs separate in anaphase I
    Sister chromatids separate in anaphase II
21
Q

For a new organism to arise sexually meiosis must occur in…

A

both parents followed by fusion of the gametes (fertilisation)

22
Q

Meiosis in a single individual produces near infinite variation, but genetic variation is further increased by:

A

Meiosis occurs in two individuals

Alleles from two organisms combine in novel ways

23
Q

benefits of genetic variation

A

Increased genetic variation produces a more resilient population that is more likely to withstand environmental change such as a disease. Genetic variation is essential for successful change by evolution.

24
Q

non-disjunction

A

homologous chromosomes fail to separate at anaphase
- Disjunction is the term used to describe the separation of chromosomes

25
Q

The result of non-disjunction is…

A

gametes that either have one chromosome too many or one too few.

26
Q

Trisomy

A

organisms with one extra chromosome (three of one chromosome instead of pair)

27
Q

Monosomy

A

organisms with one less chromosome (one chromosome instead of a pair)

28
Q

Trisomy 21

A

commonly known as Down Syndrome. The individual possesses three of chromosome 21 and 47 chromosomes in total.

29
Q

Nuchal translucency scan

A

non-invasive test, carried out between 11 and 13 weeks, an ultrasound scan looks at the nuchal fluid behind the neck of the fetus.

A large amount of nuchal fluid is strongly correlated with Down Syndrome, and the mother may be advised to have an amniocentesis or chorionic villus sample.

These tests are more invasive, but result in a karyotype of fetal cells so the parents can be sure.

30
Q

Amniocentesis

A

“amniotic fluid” & “puncture”
A sample (20 mL) of amniotic fluid is taken using a syringe.

The needle is guided by using an ultrasound.

Amniotic fluid contains cells from the fetus, and these cells are used for karyotyping.

Can be carried out in the 16th week of the pregnancy with around a 1% chance of a miscarriage

31
Q

Chorionic Villus Sampling

A

The chorion is a membrane which is a part of the placenta.

It contains many cells with villi, and some of these are taken and then cultured.

The needle is guided by using an ultrasound.

When sufficient cells have grown, a karyotype is carried out.

Can be carried out in the 11th week of the pregnancy with around a 2% chance of a miscarriage