Topic1:8 - meiosis Flashcards

1
Q

What are somatic cells?

A

body cells that are diploid and contain a full set of chromosomes

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2
Q

The number of chromosomes in a diploid cell is referred to as:

A

the diploid number.

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3
Q

describe how all chromosomes in a somatic cell occur in homologous pairs

A

All chromosomes are in homologous pairs with one copy from a paternal source and one from a maternal source.

The chromosomes of a homologous pair contain the same number and type of genes in the same location. (they code for the same trait e.g eye colour)

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4
Q

Somatic cells are formed by:

A

New somatic cells are formed by mitosis and cytokinesis and are genetically identical.

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5
Q

What are gametes?

A

sperm or egg cells which form from diploid germ-line cells by meiosis.

They:

  • are involved in reproduction.
  • are haploid cells, so they contain half the normal number of chromosomes (haploid number).

-contain only one copy from each homologous pair.

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6
Q

stages of meiosis

A

there are 2 main stages:

-meiosis 1
-meiosis 2

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7
Q

briefly summarise meiosis 1

A

-first division separates homologous pairs and produces haploid cells.

-begins after DNA replication.

-consists of Prophase1, Metaphase 1, Anaphase 1, Telophase 1
followed by cytokinesis.

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8
Q

briefly summarise meiosis 2

A

-second division separates the sister chromatids in the haploid product of meiosis 1 and results in four genetically different haploid gametes.

-begins immediately after Meiosis 1.

-consists of Prophase 2, Metaphase 2, Anaphase 2, Telophase 2
followed by cytokinesis.

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9
Q

meiosis 1 - explain what occurs in prophase 1:

A

early in prophase 1:
-replicated DNA condenses and becomes visible and the nuclear membrane breaks down.

Late in prophase 1:
-homologous chromosomes pair up
-they are placed so closely to each other that genetic material can cross over between non-sister chromatids that are part of the same homologous pair/tetrad.
-Enzymes cut and re-join the DNA of each non-sister chromatid.
-Crossing over results in the exchange of maternal and paternal gene variants and so the four chromatids are each genetically unique.

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10
Q

meiosis 1 - explain what occurs in metaphase 1:

A

-Homologous chromosomes pair up and position either side of the metaphase plate.
-Both chromosomes in a pair are attached to the same spindle fibre.
-The placement of the paternal and maternal chromosomes to each side is random and called independent assortment.
-Independent assortment is the second mechanism that can introduce genetic variation in the gametes.

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11
Q

meiosis 1 - explain what occurs in anaphase 1:

A

Spindle fibres shorten and pull apart the homologous chromosomes (each still consisting of 2 sister chromatids) to opposite poles.

<-X X->

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12
Q

meiosis 1 - explain what occurs in telophase 1:

A

new nuclear membranes form around each set of chromosomes to form 2 haploid nucleii.

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13
Q

meiosis 1 - explain what occurs in cytokinesis 1:

A

separates the cytoplasm and forms two haploid cells.
Each cell contains one set of chromosomes/one copy of each pair.

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14
Q

meiosis 2 - explain what occurs in prophase 2:

A

-Chromosomes condense and become visible.
-The nuclear membrane breaks down.
-A new spindle forms.

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15
Q

meiosis 2 - explain what occurs in metaphase 2:

A

-Each chromosomes randomly aligns on the equator so can lead to genetic variation (independent assortment).
-One chromosome attaches to each spindle fibre.

<-X-> /

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16
Q

meiosis 2 - explain what occurs in anaphase 2:

A

spindle fibres shorten and separate the non-identical sister chromatids to opposite poles of the cell.

17
Q

meiosis 2 - explain what occurs in telophase 2:

A

nuclear membranes form around each set of chromosomes.
Chromosomes decondense and are no longer visible.

18
Q

meiosis 2 - explain what occurs in cytokinesis 2:

A

the cytoplasm divides as new membranes form and 4 new haploid cells (gametes) are the final result of meiosis.

19
Q

list 4 sources of genetic variation in sexual reproduction?

A
  1. mutations
  2. crossing over
  3. independent assortment
  4. fertilisation
20
Q

briefly describe how mutations cause genetic variation in sexual reproduction

A

Mutations (spontaneous and induced) change the base sequence in DNA, making the

21
Q

briefly describe how crossing over cause genetic variation in sexual reproduction

A

Crossing over during late prophase 1 of meiosis changes the DNA base sequence in the homologous chromosomes so that each sister chromatid is genetically unique.

22
Q

briefly describe how crossing over cause independent assortment in sexual reproduction

A

Independent assortment during metaphase 1 of meiosis randomly affects how many maternal or paternal genes will end up in each gamete’s set of genetic material.

23
Q

briefly describe how crossing over cause fertilisation in sexual reproduction

A

It is a random event, as to which ovum is released, and which sperm will reach the ovum first, the resulting combinations of chromosomes provides a source of genetic variation.

24
Q

What does fertilisation result in?

A

Fusion of nuclei of haploid male and female gametes results in a new diploid cell called a zygote.

25
what is fertilisation?
Fertilisation restores the diploid number as the human zygote contains 46 chromosomes in 23 homologous pairs. (Other species have different diploid numbers) As it is a random event, as to which ovum is released, and which sperm will reach the ovum first, the resulting combinations of chromosomes provides a source of genetic variation.
26
What is genetic variation in asexual reproduction
In asexual reproduction a single parent organism divides, by either binary fission or mitosis, and produces offspring that are genetically identical to the parent organism.
27
what is budding?
Some asexually reproducing organisms reproduce by a process called budding where the adult produces a miniature offspring that separates from the parent and then grows bigger.
28
what is the source of genetic variation in asexual reproduction?
Mutation is the only source of genetic variation.