R9 mitosis and meiosis Flashcards

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1
Q

What is ploidy ?

A

The number of chromosomes in a cell

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2
Q

In terms of n, what is the karyotype ?

A

2n

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3
Q

What is the centromere and telomere in respects to cell division ?

A

Centromeres – heterochromatin, binds to the kinetochore during mitosis

Telomeres – heterochromatin, repetitive DNA, protects from degradation

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4
Q

What are sister kinetochores ?

A

Each sister chromatid have their own, they bind to the spindle fibre during mitosis

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5
Q

What is cohesin and its role in mitosis ?

A

Cohesin protein complexes hold together sister chromatid. These are then progressively removed during mitosis freeing the arms of the chromosome. The centromeric cohesin are degraded during mitosis to separate the sister chromatid.

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6
Q

How do bacteria reproduce?

A

Binary fission, asexual reproduction

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7
Q

How do mitochondria and chloroplast replicate ?

A

during mitosis they use binary fission, then are partitioned and distributed in the daughter cells, this is a form of inheritance (5th mode)

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8
Q

What is separated in meiosis 1 and 2?

A
  • Meiosis I – homologous chromosomes separated first
  • Meiosis II – sister chromatid separated.
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9
Q

What does programmed DSB achieve at the beginning of meiosis ?

A

This causes homologous chromosomes to pair up in a synaptonemal complex, this is assembled and disassembled in prophase 1, this ultimately forms a bivalent.

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10
Q

What is crossing over and a chiasma ?

A

Crossover – reciprocal exchange of chromosomal segments due to the DSB repair.
Chiasma – site of the crossover

Segregation of homologous chromosomes require at least 1 crossover. Chiasmata holds together until the SC has disassembled.

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11
Q

Why is crossing over important ?

A

causes new combinations of alleles. These are beneficial or not based on the environment.

  • Prevents accumulation of deleterious mutations
  • Recombination of X and Y is impossible, except for in the pseudo-autosomal regions located at the very ends of the arms.
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12
Q

How can we prove trans-generational inheritance of epigenetic marks in animals and plants ?

A

F2 in plants (dont set aside their germline)

F3 in animals

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13
Q

What is Spermatogenesis and oogenesis ?

A

are types of gametogenesis and they are the products of meiosis.

  • Spermatogenesis occurs constantly whereas oogenesis occurs once a month, sperm germline can mitotically divide throughout a lifetime
  • Haploid gametes will produce diploid individuals via fertilisation
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14
Q

What is DNM ?

A

Present for the first time in a family.

De novo mutation (DNM) occurring during gamete production can be inherited by offspring.

  • Older dads contribute more mutations due to the number of cell divisions in the germline
  • Maternal age influences risk of chromosomal miss-segregation.
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15
Q

What is parasexuality ?

A

acquisition of DNA (that can recombine with chromosomes or be retained as plasmids)

  • Transduction – transfer via viruses infecting bacteria
  • Conjugation – transfer via physical contact
  • Transformation – uptake from surrounding environment
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16
Q

What is gene dosage ?

A

copy number of the genes that influences the number of corresponding RNA and proteins. In us its 2.

  • Deviations (unbalanced chromosome segregation) can result in pathological conditions but also act as a driver for evolution
17
Q

What is the problem with too much or too little protein ?

A

Too little will no promote a reaction, too much will cause accumulation especially if they are involved in complexes

18
Q

What will be the expression level on the X chromosome in XX vs XY

A

They will have the same level of expression

19
Q

How is the same level of expression achieved in XY and XX

A
  • One of the two X chromosomes (XX) is completely inactivated
  • DNA methylation and repressive histone methylation = extreme packing, no expression of one of the X chromosomes. This is completely random and down to chance
20
Q

What are some methods to maintain a good gene dosage ?

A

dampening expression from both the “over-represented” chromosomes (repressive histone methylation) or ramping up expression of the “under-expressed chromosome (histone acetylation)
- Autosomes don’t have compensation mechanisms leading to higher risk of health issues.

21
Q

What happens to gene dosage in cancer cells ?

A

extensive changes in dosage due to the mutation rate being very high

22
Q

Can plants tolerate aneuploidy ?

A

Yes, seed pods can be trisomic, dosage compensation is present in some autosome

23
Q

Why does not recombination occur in mt-DNA ?

A

‘one-sided’ nature of inheritance

  • Sets of alleles are inherited in blocks (haplotypes), new haplotypes arise only via mutation which produce new alleles.
  • We cannot track back to the first male and female as they may not have been alive at the same time, won’t go back to the first human
  • They were the best at spreading their genes.