Unit 3 - Meiosis & Genetics Flashcards

1
Q

Describe what occurs during “crossing over”, including when it occurs.

A

Occurs during prophase 1 of Meiosis

Is the process where homologous chromosomes pair up with each other and exchange different segments of their genetic material to form recombinant chromosomes

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2
Q

If an organism’s diploid number is 36, its haploid number is _____.

A

18

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3
Q

What are the two main sources of genetic variation?

A
  1. Random (independent) assortment of genes during meiosis
  2. Crossing over during meiosis 1
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4
Q

What’s taking place in the diagram?

A

Crossing over

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5
Q

A woman that is heterozygous for widow’s peak and heterozygous for freckles mates with a man that is also heterozygous for both traits. What is the phenotypic ratio of their possible offspring?

A

9:3:3:1

9 with freckles AND widow’s peak

3 with freckles and no widow’s peak

3 with widow’s peak and no freckles

1 with neither widow’s peak nor freckles

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6
Q

The passing of characteristics from parents to offspring

A

Heredity

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7
Q

The study of the passing of characteristics from parents to offspring

A

Genetics

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8
Q

Who was the father of modern genetics?

A

Gregor Mendel

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9
Q

Differentiate between true breeding and hybrid breeding.

A

True breeding creates offspring identical to each other and the parents

Hybrid breeding creates offspring that are different.

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10
Q

What did Mendel determine?

A

That biological factors (genes) are passed from parents to offspring.

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11
Q

The principle of dominance states that

A

Some alleles are dominant and some are recessive

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12
Q

Hair color and eye color are examples of ______, while blonde, brunette, blue, and green are examples of ______.

A

Genes

Alleles - different versions of a gene

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13
Q

How many alleles for each gene does a gamete possess?

A

1

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14
Q

Compare and contrast the terms homozygous and heterzygous.

A

Homozygous describes genotypes where both alleles are the same (ex. TT or tt)

Heterzygous describes genotypes where the alleles are different (ex. Tt, Hh, AB)

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15
Q

How do genotype and phenotype relate?

A

Genotype is the actual genes (ex. TT, Tt, tt)

Phenotype is the physical expression of the genes (ex. tall or short)

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16
Q

What are punnett squares used for?

A

Used to determine the gene combinations that might be possible from a genetic cross

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17
Q

What can’t be determined from a punnett square?

A

The actual results of a genetic cross.

18
Q

The Law of Independent Assortment states that

A

alleles of different genes separate independently of each other during gamete formation

19
Q

True or false: genes on different chromosomes are related.

A

False: genes on different chromosome are not related in any way.

20
Q

What is meant by the term “polygenic” and why is it significant?

A

The trait is controlled by many genes, as opposed to a single gene, and the expression of the trait contains a lot of variety (ex. hair color, skin color, eye color, height)

21
Q

What is incomplete dominance?

A

A form of inheritance in which the dominant trait does not completely mask the appearance of the recessive trait. Blending of the dominant and recessive traits occurs with heterozygous individuals.

22
Q

What is codominance?

A

With codominant traits, both alleles contribute to the expression of the gene so both forms of the gene are shown in the phenotype.

Ex. roan cattle, erminette chickens.

23
Q

What form(s) of inheritance is exhibited by human blood types?

A

both codominance and multiple alleles

24
Q

A form of inheritance in which there are multiple alleles for a single gene trait

A

Multiple Alleles

25
Q

Traits that are produced by the interaction of several genes

A

Polygenic traits

26
Q

What does each symbol on a pedigree represent?

A

Square - male

Circle - female

Horizontal line - married couple

Vertical line - offspring

Filled in square/circle - possesses the trait

Half filled in square/circle - carrier of the trait

Slash - deceased

27
Q

This form of inheritance does NOT skip generations (for a child to have it, at least one of their parents must have it), and is found in males and females in equal numbers

A

Autosomal Dominant

28
Q

This form of inheritance DOES skip generations (a child can have it without the parent having it) and is found in males and females in equal numbers

A

Autosomal Recessive

29
Q

Describe the characteristics of sex-linked (x-linked) traits.

A
  • Mostly found in males
  • If father has it then daughter has it OR is carrier
  • If the son has it then the mother is a carrier
  • Is carried on the x chromosome
30
Q

Describe the products of meiosis.

A

4 genetically unique haploid cells (N), each with 23 chromosomes.

31
Q

How many chromosomes do sex cells (gametes) contain?

A

23

32
Q

The two types of gametes are

A

Sperm and egg cells!

33
Q

How does meiosis differ in males and females?

A

In males - produces 4 sperm cells

In females - produces 1 egg and 3 polar bodies

34
Q

Reductive cell division

A

Meiosis

35
Q

Compare and contrast haploid and diploid

A

Haploid - cells that contain half the normal chromosome count, represented by the symbol “N”, are gametes

Diploid - cells that contain the full chromosome count, represented by the symbol “2N”, are somatic cells

36
Q

When are the homologous pairs separted?

A

During Anaphase I

37
Q

When are the sister chromatids separated (during meiosis)?

A

During Anaphase II

38
Q

How might a human cell end up with an incorrect chromosome number at the end of meiosis?

A

Through nondisjunction.

39
Q

What is nondisjunction and what is the term for cells that suffer from this phenomenon?

A

Nondisjunction is a failure of chromosomes to separate correctly.

Cells that suffer from this possess aneuploidy, an abnormal chromosome number.

40
Q

What is a karyotype and what is it used for?

A

A karyotype is a picture of a person’s chromosomes.

It can be used to detect an extra or missing chromosome, and indicate if an individual is male or female.

41
Q

What chromosomes would you expect to find in a human egg cell?

A

22 autosomes and an X chromosome

42
Q

Which chromosomes would you expect to find in a human sperm cell?

A

22 autosomes and a Y chromosome