Meiosis and Genetic Inheritance Flashcards

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1
Q

Meiosis

A

Form of cell division that creates gametes that are suitable to be paired sexually with another gamete to contribute genetic information to the next generation

Germ cells undergo two rounds of nuclear division to produce four haploid daughter cells called gametes- unique genetic makeup

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2
Q

Process of Meiosis

A

Two rounds of division called meiosis I and meiosis II

Each consists of successive stages of prophase, metaphase, anaphase, and telophase

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3
Q

Meiosis I

A

Separate homologous chromosomes to produce two haploid cells, each with one copy of the 23 chromosomes

Known as reduction division

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4
Q

Prophase I

A

Homologous chromosomes line up alongside each other, matching genes exactly
Have four chromatids in homologous pair, called tetrads

Crossing over may occur, genetic recombination

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5
Q

Crossing Over or Genetic Recombination

A

Chromosomes “zip” along each other where nucleotides are exchanged forming the synaptonemal complex
- creates ‘X’ shape or chiasma under microscope

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6
Q

Gene Linkage

A

Where genes are physically located near one another, increasing probability that traits will be inherited together despite crossing over

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7
Q

Single Crossover

A

Chromosomes may exchange sections of genetic information just once

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8
Q

Double crossover

A

Chromosomes trade a segment once and then trade back a sub-section of segment
Each chromosome retains some of own original genetic material

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9
Q

Gene mapping

A

A technique which helps determine locations and relative distances of genes on chromosomes

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10
Q

Metaphase I

A

Two homologues remain attached and move to the metaphase plate
- Tetrads align along the plate with 23 tetrads in single file line in humans

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11
Q

Anaphase I

A

Homologous chromosomes each separate from their partner independently assorting to create two haploid cells

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12
Q

Telophase I

A

Nuclear membrane may reform, cytokinesis may occur
- these both occur in humans

New germ cells are haploid with 23 replicated chromosomes and are called secondary spermatocytes or secondary oocytes

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13
Q

Polar Body

A

Produced in female oocytes

One of the germ cells formed after telophase I becomes a polar body, has much less cytoplasm, and degenerates

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14
Q

Meiosis II

A

Proceeds through Prophase II, Metaphase II, Anaphase II, and Telophase II much like mitosis under light microscope

Final products are haploid gametes, each with 23 chromosomes
Four spermatocytes formed
One ovum is formed

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15
Q

Nondisjunction

A

During Anaphase I or II, if any chromosome does not split
Anaphase I: One cell has two extra chromatids and other is missing a chromosome
Anaphase II: Results in one cell having one extra chromatid and one cell lacking a chromatid

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16
Q

How does trisomy 21 happen?

A

Known as Down syndrome

Caused by nondisjunction of chromosome 21 in Anaphase I

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17
Q

Gametogenesis

A

Production of gametes

Different for males than for females

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18
Q

Gametogenesis in Males

A

Diploid progenitor cells called spermatogonia.
Spermatogonium undergoes mitosis to produce two diploid primary spermatocytes
Primary spermatocytes undergo meiosis I to become haploid secondary spermatocytes
Secondary spermatocytes undergo meiosis II to become spermatids
Spermatid loses cytoplasm and gains tail- sperm

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19
Q

Male gamete

A

Sperm

20
Q

Gametogenesis in Females

A

Diploid progenitor cell is oogonium
Oogonium undergoes mitosis to produce two primary oocytes before female is born
At puberty, primary oocytes undergo meiosis I, making haploid secondary oocyte
Secondary oocyte arrested at metaphase II until penetrated by sperm (fertilization), complete meiosis II to form ootid, mature into ovum

21
Q

Why does the female oocyte need to conserve cytoplasm by releasing polar bodies?

A

Once an ovum is fertilized, resulting zygote needs to undergo many rounds of division before it is able to implant on the uterine wall and establish a blood supply
Increased cytoplasm present in ovum provides nutrients necessary to sustain a zygote as it becomes a bastula and travels from fallopian tube to uterus

22
Q

Genetic Leakage

A

Flow of genetic information from one species to another

23
Q

Locus

A

Position on a chromosome

24
Q

Wild type

A

Normal or most common allele type for a certain trait within a population

25
Q

Genotype

A

Individual’s genetic makeup of a certain trait or allele

26
Q

Phenotype

A

Expression of the trait of an allele

Expressed through the action of enzymes and other structural proteins which are encoded by genes

27
Q

Complete dominance

A

Dominant allele masks expression of the recessive allele

Mendel’s pea plants, purple vs. white

28
Q

Homozygous

A

Individual with a genotype having two dominant or two recessive alleles that are the same

29
Q

Heterozygous

A

Individual with a genotype having one dominant and one recessive allele

AKA hybrid

30
Q

Law of Segregation

A

Mendel’s first law of Heredity

Alleles segregate independently of each other when forming gametes during meiosis

31
Q

Penetrance

A

Refers to the probability of a gene or allele being expressed if it is present

Penetrance of dominant allele is 100%

32
Q

Expressivity

A

Measure of how much the genotype is expressed as a phenotype
Degree of expression
Relevant when considering incomplete dominance (intermediate phenotypes)

33
Q

Incomplete dominance

A

When a heterozygous individual exhibits a phenotype that is intermediate between its homozygous counterparts

34
Q

Co-dominance

A

Heterozygous individual exhibits both phenotypes

E.g. Human blood type alleles are co-dominant because a heterozygous individual exhibits A and B antigens

35
Q

Punnett Square

A

Predicting genotypic ratios of offspring from parent genotypes

36
Q

Law of Independent Assortment

A

Mendel’s Second Law of Heredity

Genes located on separate chromosomes assort independently of each other

For example, genes that code for distinct traits when located on separate chromosomes do not affect each other during gamete formation

37
Q

Dihybrid Cross

A

Cross that can be demonstrated on a Punnett square for two distinct traits with a dominant and recessive allele for each in which we cross all possible heterozygous combinations with one another (WG, Wg, wG, wg) x (WG, Wg, wG, wg)
Phenotypic ratio: 9:3:3:1

38
Q

Sex Chromosome

A

Each partner in the 23rd pair of chromosomes (X or Y)

Y chromosome contains only a few genes

39
Q

Sex-linked trait

A

Genes located on the sex chromosomes (usually the X chromosome, because the Y chromosome has very few genes)

In males sex-linked genes on X chromosome are expressed whether dominant or recessive

40
Q

Barr body

A

Most somatic cells have one of the X chromosomes in a female randomly condense to forma tiny dark object

Formed at random, so active allele is split approximately evenly among all cells
- recessive allele usually still only displayed in homozygous individual

41
Q

Carrier

A

Female may have recessive trait on 23rd pair of chromosomes without expressing it
- strong chance of being expressed in male offspring

42
Q

Hardy-Weinburg Equilibrium

A

Theoretical state of suspended evolution in which there is no net change happening in allelic frequencies over time

43
Q

Hardy-Weinburg equation

A

p^2 + 2pq + q^2 = 1

Equation predicts genotype frequencies of a gene with only two alleles in a population in Hardy-Weinberg equilibrium

44
Q

Difference between Mendel’s calculations and Hardy-Weinberg equation?

A

Rather than having a 1 in 2 chance of inheriting an allele (A or a) from one of the two parents, here the probability corresponds to the proportion of that allele (A or a) in entire population

45
Q

Gametes

A

Haploid reproductive cells