Meiosis Flashcards

1
Q

What is another word for haploid cell?

A

Gamete

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2
Q

What kind of gamete is associated with birth defect and infertility in humans?

A

Aneuploid Gamets

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3
Q

What are the meiotic contributors to genetic diversity in populations?

A

Recombination and redistribution of homologous chromosomes

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4
Q

Are the daughter cells haploid or diploid after meiosis 1?

A

Haploid (2)

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5
Q

What happens in Meiosis 2?

A

Sister chromatids segregate, leading to the formation of four non-identical haploid gametes.

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6
Q

What is the difference between a homologue and sister chromatids?

A

Homologues - Starting diploid cell involving two different chromosomes

Sister Chromatids - an identical pair of chromosomes made by replication

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7
Q

Why is the fact that meiosis is reductive necessary?

A

It halves the number of chromosome sets that originally are doubled by fertilization

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8
Q

Are the diploid cells that remain after Meiosis 1 homologous or sister chromatids?

A

Homologous

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9
Q

What is the order of segregation in terms of the type of chromatids?

A

Homologous chromosomes segregate first, and sister chromatids segregate after

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10
Q

How do some protists and fungi fit into the cell cycle?

A

They live as haploid cells, and only undergo mitosis in the upper part of the cycle, skipping the diploid generation

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11
Q

How do humans fit into the cell cycle?

A

They live as diploid cell, and only undergo mitosis in the lower part of the cell cycle, skipping the haploid generation

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12
Q

How do plants fit into the cell cycle?

A

They have two distinct multicellular generations (alternation of generations), they undergo mitosis in both sides of the cell cycle

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13
Q

How are haploid ESCs (embryonic stem cells) different than diploid ones?

A

Haploids have smaller volume, they only have one expressed X chromosome, and can differentiate

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14
Q

In yeast, what phase triggers mitosis and which regulators trigger it?

A

In the G1 phase IME (inducer of mitosis) 1 and 2 promote entry into the mitotic S phase

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15
Q

What are the roles of IME 1 and 2?

A

IME 2 encodes a CDK-like protein in G1 phase which regulates IME 1 transcription, which transcribes the meiotic program

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16
Q

What is the difference in CDK levels in mitosis and meiosis?

A

There is a second peak of levels (of IME2 and therefore CDK) in meiosis

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17
Q

Why do meiotic CDK levels drop between Meiosis 1 and 2?

A

It prevents further DNA replication

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18
Q

What is the difference in the amount of time it takes for male vs female mice to undergo the first meiotic prophase?

A

10 days for males, roughly 4 days for females ( but the oocytes arrest for months)

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19
Q

What triggers the transition from a mitotic to meiotic cell cycle?

A

Endogenous programmed events

20
Q

What substance is the key inducer of meiosis?

A

Retinoic Acid (RA)

21
Q

What two key targets does RA hit after diffusing into the germ cell?

A

It transcribes the target genes (Stra8 is critical) and transcribes meiosin, a gene essential for mitosis - meiosis transition

22
Q

What do epigenetic modifiers in chromatin coordinate with to activate downstream targets?

A

Stra8 and meiosin

23
Q

How was meiotic gene regulation studied 1980-2000?

A

Genetic screening was done on mutants with meiotic defects

24
Q

How was meiotic gene regulation studied 2000-2020?

A

Transcriptome profiling is the use of RNA to understand gene expression and links to physical differences

25
Q

Briefly explain the modern genomic assays findings?

A

They detail regulatory mechanisms that govern gene expression

26
Q

Name and briefly explain the 5 steps of meiotic prophase

A

Leptotene - Condensation of chromosomes
Zygotene - pairing of homologues into tetrads
Pachytene - Thickening of chromosomes and crossing over
Diplotene - Separation of chromosomes
Diakinesis - Chromosomes condense, nuclear envelope breaks down

27
Q

What is the general mechanism for Homologous recombination (HR)?

A

It is the DNA response to genetically programmed double strand breaks

28
Q

What model do we follow for meiotic recombination?

A

The Early Crossover Decision (ECD) model

29
Q

What are the two options for the ECD model?

A

It can go the NCO (non crossover) or CO (crossover) pathway

30
Q

What direction of resection does the DNA follow in crossing over?

A

the 5 to 3 direction

31
Q

What are the differences in the NCO and CO pathways?

A

It depends where the Holliday Junctions are cut

32
Q

How can we get a good estimate of chromosome length?

A

The frequency of recombination is a fair estimate of gene length, they are proportional to each other

33
Q

Define recombination

A

The process that results in gametes with different alleles than the parental generation

34
Q

What is the frequency of recombination?

A

The number of crossover events in the section of the genome per meiosis (0-1)

35
Q

What is a recombination hotspot?

A

Regions with a higher frequency of recombination than elsewhere

36
Q

What are 4 features of human hotspots?

A
  1. They have rates hundreds of times higher than surrounding
  2. They are found near telomeres and in certain gene rich areas
  3. More than 30,000 have been identified in the human genome
  4. It is where cancer and other diseases are located due to genetic instability
37
Q

What enzyme removes coheisins from sister chromatids during the onset of anaphase?

A

protease separase

38
Q

What complex activates separase?

A

APC (anaphase promoting complex)

39
Q

Why do centromeric rings of coheisins persist through meiosis 1?

A

So sister chromatids can co-segregate

40
Q

What allows for the separation of sister chromatids in anaphase 2?

A

Separase dissociates the coheisins around sister chromatids

41
Q

What are the study results in terms of cells affected by poor meiosis?

A

1 in 4 sperm cells and 1 in 12 eggs have mutations

42
Q

What are the complications an aneuploidy?

A

Infertility, miscarriages, and birth defects

43
Q

What is the leading cause of mental developmental issues?

A

Aneuploidy

44
Q

What are the three ways meiosis can affect human health adversely?

A
  1. Re-expression of remnant miotic proteins can have oncogenic consequences
  2. Aneuploid cancer cells are very prevalent
  3. Genetic recombination can change pathogen properties, factoring into treatment and vaccination equations