IDK BUT DEFINETLY NOT W10 Flashcards

1
Q

What do mutations cause?

A

Mutations result from mistakes in DNA replication or from unrepaired damaged DNA

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2
Q

What may mutations be caused from?

A
  • reactive molecules produced through the normal course of metabolism
  • chemicals in the environment
  • radiation
  • gene sequences that can jump from one position to another in a genome
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3
Q

Are nucleotide substitutions mutations common?

A

No they are relatively rare

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4
Q

Why do RNA viruses and retroviruses have high rates of mutations?

A

Because RNA is a less stable molecule than DNA. Also the replication if these genomes lacks a proofreading function

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5
Q

What is the average mutation rate?

A

10^-10, therefor one in every 10 billion is mistakenly substituted for another

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6
Q

Define hotspots

A

certain nucleotieds that are especially prone to mutation and can exhibit rates of mutation greater than the average.

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7
Q

True or false, the rates of mutations differ between sexes

A

True

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8
Q

How does the rate of mutations differ between somatic and germline cells?

A

In mammals the rate of mutation per nucleotide per replication is greater in somatic cells than germ cells

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9
Q

What does the rate per genome depend on?

A

The size of the genome and the number of cell divisions per generation

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10
Q

In humans what is the average number of newly arising nucleotide base substitution per genome in one generation?

A

30 or 60 per diploid zygote

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11
Q

Why are humans able to withstand a larger number of mutations per genome?

A

because only 2.5% of the genome codes for proteins

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12
Q

Which rate of mutation is more relevant to somatic cells?

A

the rate of mutation per nucleotide substitution per replication. This is cause they do not effect future generations

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13
Q

Which rate of mutation is more relevant to germline cells?

A

rate of mutation per genome per generation. germline cells pass on mutations from generation to generation in an evolutionary process

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14
Q

What are the two main mutations that can cause cancer?

A
  • the mutation increases the activity of a gene that promotes cell growth and division
  • the mutation decreases the activity of a gene that restrains cell growth and division
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15
Q

What is the first hypothesis regarding how mutations arise?

A

Mutations occur without regard to an organisms needs

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16
Q

What is the second hypothesis regarding how mutations arise?

A

There is some sort of feedback between the needs of an organism and the process of mutation, and the environment directs specific mutations that are beneficial to the organism.

17
Q

True or false, Most DNA damage or errors in replication are immediately removed or corrected by specialized enzymes in the cell

A

true

18
Q

What happens if a change in DNA escapes correction by DNA repair systems?

A

The change becomes stable and is sub-sequentially inherited through mitotic or meiotic division

19
Q

Define nucleotide substitution/point mutation

A

A mutation in which one base air is replaced by a different pair

20
Q

Define synonymous/silent

A

A mutation resulting in a codon that does not alter the corresponding amino acid in the polypeptide

21
Q

Define non-synonymous/missense mutations

A

A point mutation resulting in a change of amino acid

22
Q

What causes sickle cell anemia?

A

When an individual inherits two mutant B globin genes

23
Q

Define a nonsense mutation?

A

A mutation that creates a stop codon, terminating translation

24
Q

Define frameshift mutations

A

A mutation in which an insertion or deletion of some number of nucleotides that is not a multiple of three, causes a shift in the reading frame of mRNA, therefor changing all following codons

25
Q

What are transposable elements or transposons?

A

A DNA sequence that can replicate and move from one location to another in a DNA molecule

26
Q

What is one method of transposition as outlined by the corn kernel experiment?

A
  • A cut and paste mechanism
  • The transposon is cleaved from it original location in the genome by a specific enzyme (transposase) and inserted in a different position
27
Q

What is another method of transposition not outlined by the corn kernel experiment?

A

Transposition via a RNA intermediate.When these types of transpoable elements move (retrotransposons) retrotransposon used as a template for transcription stays behind in its original location.

28
Q

What is a duplication?

A

Is a chromosomal mutation where one region of the chromosome is present twice

29
Q

What is a deletion?

A

Is a chromosomal region where one region is missing

30
Q

What may cause deletion?

A
  • An error in replication

- From joining breaks in a chromosome that can occur on either side of a deleted region

31
Q

Why can a deletion survive and persist within a population?

A

Because chromosomes are present in homologous pairs

32
Q

What is the relationship between the size of a deletion and survival?

A

Generally the larger the deletion the smaller the chance of survival.This is because organisms are sensitive to dosage (or number of copies of each gene)

33
Q

What role does small duplications play in the origin of genes and evolutionary divergence?

A

It allows one copy of the gene to change without threat to the survival of the organism. Therefor a new copy of the gene may increase survival chances and reproduction.

34
Q

What is duplication and divergence?

A

The process of creating new genes from duplicates . with the term duplicates referring to the accumulation of differences between the duplicate genes that occurs on an evolutionary time scale.

35
Q

How can duplications affect gene families?

A

Multiple rounds of duplication and divergence can giver rise to a group of genes with related functions known ad gene families

36
Q

What are inversions?

A

Chromosomal mutations where the region between two breaks in the chromosome is flipped in orientation before being repaired

37
Q

How does the accumulation of inversions over time affect evolution?

A

The accumulation of inversions over evolutionary time explains in part why the order of genes along a chromosome can differ even among closely related species.

38
Q

What is a reciprocal translocation?

A

When two non-homologous undergo an exchange in parts.Both chromosomes are broken and the terminal segments are exchanged before the breaks are repaired

39
Q

How can reciprocal translocation affect meiosis?

A

Both chromosomes involved may not move together in the same daughter cells , resulting in gametes with only one part of the reciprocal translocation. This affects gene dosage because these gametes have extra copies of genes in one chromosome and are missing genes in the other