3.3 meiosis Flashcards

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1
Q

define meiosis

A

the reduction division of a diploid cell to produce 4 haploid daughter cells

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2
Q

identify the main differences between meiosis 1 and meiosis 2

A

meiosis 1:

-involves the separation of homologous chromosomes (bivalent/ tetrads)
-is a reduction division (diploid to haploid)
-promotes genetic variation (crossing over random assortment)

meiosis 2:
-involves the separation of sister chromatids
-is a mitotic division (haploid to haploid)
-does not promote genetic variation

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3
Q

differentiate between homologous chromosomes and sister chromatids

A

Homologous chromosomes are the maternal and paternal copies of a given chromosomes

homologous chromosomes have the same structure and the same genes at the same loci positions

sister chromatids are the duplicated copies of the chromosome’s DNA (copied during S phase of interphase)

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4
Q

compare the processes of meiosis and mitosis

A

meiosis:
type of cell produced: sex cells (gametes)
number of cells produced: 4
number of divisions: 2
ploidy of daughter cells: haploid
genetics of daughter cells: shows genetic variation

mitosis:
body somatic cells
2
1
diploid
are genetically identical

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5
Q

outline how crossing over and independent assortment give rise to infinite genetic variety

A

crossing over:

-crossing involves the exchange of genetic material between non sister chromatids of a bivalent

-bivalents are connected at points called chiasma during the process of synapsis (during prophase 1)

-it is at these chiasma that recombination occurs

independent assortment:

bivalents will line up at the cell’s equator in a random orienatation
during metaphase 1

meaning there is equal probability of a gamete containing the maternal OR paternal copy for any chromosome pair

Because human cells have 23 chromosome pairs, there are 2^23 possible chromosomes combinations
(equates to over 8 million different gamete combinations)

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6
Q

explain how random gamete fusion promotes variation within a species

A

when two haploid gametes fuse, they form a diploid zygote which can grow into a new organism

because gamete fusion is random, each successive offspring will be composed of a distinct combination of maternal and paternal chromosomes

this means every member of a species is unique (promoting biodiversity)

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7
Q

explain how non disjunction can give rise to aneuploidy

A

non disjunction describes the failure of chromosomes to separate during cell division

if non disjunction occurs in anaphase 1, all 4 gametes will be affected

if non disjunction occurs in anaphase 2, only 2 of the gametes are affected

if a gamete with one extra chromosome fuses with a normal gamete, the offspring will have trisomy

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8
Q

list the genetic condition that causes Down syndrome

A

is caused by trisomy 21
increased maternal age increases the risk of non disjunction

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9
Q

describe the method by which cells are obtained for karyotyping

A

cells are isolated and treated with drugs to promote cell division (makes chromosomes visible to microscope)

cells are arrested during mitosis and then chromosomes are isolated and visualized

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10
Q

compare the benefits and risks associated with amniocentesis and chorionic villi sampling

A

amniocentesis:

cells are extracted from the amniotic fluid

occurs later in pregnancy (~15 weeks) but has a slightly lower risk of miscarriage (~0,5%)

chorionic villi sampling:

cells are extracted from the placenta (chorionic villus)

occurs earlier in the pregnancy (~11 weeks) but has a slightly higher risk of miscarriage (~1%)

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