Genetics Flashcards

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1
Q

Define a mutation

A

Any change in DNA that may result in a new phenotype

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2
Q

Explain where germ cell mutation occurs and if it affects the organism or the offspring (and why that is)

A

Occurs in the gametes. Doesn’t affect organism but is passed to offspring because it’s on the sex cells which a child gets one from mom and one from dad.

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3
Q

Germ cell mutations provide the __________ on which ____________________ acts

A

Variation, natural selection

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4
Q

Explain where somatic cell mutation occurs and if it affects the organism or the offspring (why)

A

Occurs in the body cells, is passed to daughter cells by mitosis (affects organism)

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5
Q

List the 4 types of chromosomal mutations

A

Deletion, inversion, translocation, nondisjunction

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6
Q

Define deletion mutation and be able to draw picture of it

A

A piece of chromosome is deleted PICTURE

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7
Q

Define inversion mutation and draw picture

A

A section of chromosome breaks off and reattaches in the opposite direction PICTURE

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8
Q

Define translocation mutation and draw picture

A

A section breaks from one chromosome and attaches to another PICTURE

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9
Q

Define nondisjunction mutation and be able to draw a picture of it

A

When chromosome pairs fail to separate during meiosis PICTURE

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10
Q

Describe difference in origin from monosomy and trisomy in nondisjunction

A

Mono: when a zygote has only one chromosome of a pair (turners syndrome)
Tri: when a zygote has 3 of a particular chromosome (downs)

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11
Q

Define gene mutations

A

May involve a single nitrogen base or a larger segment of a gene

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12
Q

Differentiate between chromosome mutations and gene mutations

A

Chromosome only has the mutation of one specific chromosome, while gene mutations involve nitrogen bases or larger segments of genes.

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13
Q

List the two types of gene mutations and draw picture

A

Point mutation

Frame shift mutation

PICTURES

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14
Q

Identify and justify why which of the two types of gene mutations would lead to the largest change in the genetic code of an organism

A

The frame shift mutation because (insert pictures of both frame and point mutations) the frame shift changes every single amino acid after the first 3 while the point only changes one amino acid in the whole thing

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15
Q

Define mutagen

A

Factors that cause mutations

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16
Q

List the five examples of mutagens listed in class

A

Sunlight, cig tar, asbestos, radiation, some viruses

17
Q

Explain the purpose of the Ames test

A

It’s a test used to identify mutagens

18
Q

Describe the purpose of a pedigree

A

Too show how a trait is inherited over several generations

19
Q

Define carrier

A

Someone who is heterozygous. They don’t show the recessive trait but they can pass it to their offspring

20
Q

Define single allele trait

A

Homozygous recessive (2 rec alleles to show trait), codominant,

21
Q

Explain the difference between a dominant and a recessive trait

A

The dominant trait always is the one that shows in the phenotype if it is present in the genotype.
The recessive trait only shows up if you have both recessive alleles in genotype

22
Q

Define codominant allele

A

If you are heterozygous for this genotype, you will express both phenotypes

23
Q

Define incomplete dominance

A

Dominant allele is not completely dominant over the recessive allele, a blending of the phenotypes is seen

24
Q

Define polygenic trait

A

Trait that is controlled by 2 or more genes (skin color, eye color, fur color in labs)

25
Q

Define multiple allele trait and identify a human trait that is multiple allele

A

3 or more alleles of the same gene code for a single trait

Blood type (ABO)

26
Q

Define sex linked trait

A

Genes for these traits are found on the sex chromosomes (X)

27
Q

Define sex limited trait

A

Autosomal-not found on X or Y chromosome

Phenotype appears only in one gender

28
Q

Define sex influenced trait

A

Traits that are influenced by the presence of male or female hormones (baldness)

29
Q

Define genetic screening

A

Examination of a persons genetic makeup (karyotype, amniocentesis, fetoscopy)

30
Q

Identify and describe the 5 tests used for genetic screening

A

Karyotype- analyze chromosome images
Amniocentesis- test amniotic fluid for chromosomal abnormalities
Fetoscopy- scope inserted into uterus to view fetus
Ultra sound- noninvasive view of fetus
Chorionic villi sampling- test villi from placenta

31
Q

Define evolution

A

The change in the allelic frequency of a gene in a population over time

32
Q

Identify the two scientists and what they contributed to the modern theory of evolution

A

Darwins “survival of the fittest” through natural selection explains species variation, but not individual variation

Mendel use of alleles and inheritance explain individual variation not species variation

Together thy cover everything

33
Q

Explain the difference between scientific law and scientific theory

A

A scientific law is a statement based on repeated experimental observations that describes some aspect of the universe. (Doesn’t explain why)

A scientific theory is a well-substantiated explanation of some aspect of the natural world, based on a body of facts that have been repeatedly confirmed through observation and experiment. (Explains why)

34
Q

Define polymorphisms and list examples

A

Phenotypic differences within a species.

Butterfly colors, skin color, beak sizes

35
Q

Differentiate between variation in chromosomes, protein structure, and nucleotide sequence, and know which lab method is used for each

A

Chromosomes: banding pattern differences of chromosomes

Protein structure: use gel electrophoresis to move proteins based on size

Nucleotide: DNA sequencing is used to identify changes in nucleotides