Heredity Flashcards

(31 cards)

1
Q

Define genetics.

A

The study of heredity, which studies inherited traits

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2
Q

List some examples of inherited traits.

A
  • height
  • eyes
  • hair
  • shape of nose
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3
Q

List some examples of acquired traits.

A
  • weight
  • tan
  • accent
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4
Q

Define a phenotype.

A

A visible/measurable trait that is passed on

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5
Q

Define a genotype.

A

Traits controlled by genes and found in every cell in the body

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6
Q

Discuss the connection between chromosomes and genes.

A
  • each chromosome can have one million or more genes, one for each trait
  • the more important genes are closer to the center
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7
Q

What is the difference between homozygous and heterozygous genotypes?

A

Homozygous are two of the same traits, or a pure individual; heterozygous are two different traits, one being dominant, called a “hybrid individual”

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8
Q

Give the scientific terms for different generations.

A

Parents: P generation
Parents’ offspring: F generation
Offsprings’ offspring: F2 generation, etc.

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9
Q

Who was Gregor Mendel?

A

An Austrian monk who studied math and science the mid 1800s; known as the “father of genetics” and investigated genetics at the organism level by studying pea plants

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10
Q

What are some of Gregor Mendel’s discoveries?

A
  • offspring traits were never intermediate (a mix of both), and only resembled one parent
  • true breeding: all the same traits in all offspring
  • not true breeding: some offspring have different traits
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11
Q

What is the theory of inheritance?

A
  • offspring inherit alleles from parents, which code for traits
  • each offspring has two alleles for each trait
  • the position on the chromosome where the allele is located is called loci, or a locus
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12
Q

What are the two laws of inheritance?

A

1) law of segregation
- each individual has two alleles for each trait
- each gamete has one allele
- alleles of paretns combine during fertilization in different but predictable combinations
- the phenotype doesn’t blend, but is either on or the other

2) law of individual assortment of alleles
- alleles of different traits pass to offspring independently
- alleles controlling different genes are randomly distributed to gametes
- e.g. the colour of a pea pod does not affect the texture
- except for alleles located on the same chromosome, which are inherited together (e.g. red hair and freckles)

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13
Q

Define complete dominant inheritance.

A

When a heterozygous phenotype is intermediate between two phenotypes; the traits blend (e.g. red flower and white flower becomes a pink flower)

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14
Q

Define codominant inheritance.

A

Two dominant traits are both expressed in offspring (e.g. white flower and purple flower become a white and purple striped flower)

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15
Q

Discuss multiple alleles.

A

Due to mutations or other chromosomal changes, an allele may alter its form and express a slightly different phenotype; a new allele is created, and two or more alleles exist for a specific trait (e.g. humans have three different blood types, A, B, and O)

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16
Q

Define an autosome.

A

All chromosomes (pairs 1-22) except the sex chromosomes, which are the twenty-third pair

17
Q

What are sex-linked genes?

A

Traits located on the X or Y chromosomes; because the X chromosome is much larger, more traits are carried on it than on Y

18
Q

Explain why men are more likely to get X-chromosome traits.

A

Because there are more traits on the X chromosome than the Y; therefore, because men only have one X chromosome, those traits are determined by only one allele

19
Q

How many base pairs do X and Y chromosomes have?

A

X: 153 million
Y: 50 million

20
Q

What are some X-related genetic conditions?

A
  • Hemophilia (blood can’t clot)
  • colour blindness
  • Juvenile muscular dystrophy
21
Q

Define polygenetic inheritance.

A

A trait controlled by two or more sets of alleles, which may be on different chromosomes; each dominant allele has a quantitative affect on the phenotype, and results are cumulative (e.g. eye colour can be light to dark brown)

22
Q

Discuss the relationship between genes and the environment.

A

The environment of an organism affects the phenotype; some traits make the organism more successful than others (e.g. colours that camouflage)

23
Q

Define genetic mutations and list the two types.

A

Changes in genetic information that become part of the individual’s genotype
- Somatic: passed to the descendants of cells within the organism, but not passed to offspring (e.g. some cancers)
- Reproductive: passed on to gametes, then on to offspring

24
Q

Define mutagens and list some examples.

A

Environmental factors that cause genetic mutations
- very high temperatures
- viruses
- chemicals
- radiation

25
What are the two kinds of mutations?
Chromosomal and genetic
26
Discuss some kinds of chromosomal mutations.
Affect the whole chromosome - Nondisjunction: homologous chromosomes don't separate, so one gamete has one extra chromosome while the other has one less - Sex chromosome nondisjunction: on either the X or Y chromosome; some gametes have XX or XY while others have no sex chromosomes
27
Define trisomy and monosomy.
Trisomy: after fertilization, the organism has one extra chromosome Monosomy: after fertilization, the organism has one missing chromosome
28
List some kinds of sex chromosome nondisjunction.
XXX - super female XXY - Klinefetter's syndrome XYY Y - zygote not viable X - Turner's syndrome YY - superman syndrome
29
Discuss autosomal chromosome nondisjunction.
- if monosomy occurs, a zygote cannot survive; all pairs are necessary - if trisomy occurs, most do not survive; only five small chromosomes can have trisomy and still allow the zygote to survive - when trisomy occurs in chromosome pair 21, it causes Down's Syndrome
30
Discuss polyploidy.
- a gamete receives two sets of the same chromosomal pair - lethal in animals, but common in plants
31
List the four kinds of chromosomal rearrangement.
- deletion: a piece of a chromosome breaks off, and the genetic information is lost - duplication: a piece of a chromosome is repeated and there is extra genetic information, which may cause problems - inversions: a segment of the chromosome flips upside down, which can cause problems if genes cannot interact - translocation: genes are transferred from one chromosome to another, which causes less severe problems