Chapter 9: DNA Structure and Replication Flashcards

1
Q

DNA Polymerase

A

Catalyzes the addition of nucleotides as the new DNA chain grows to the 3’ end of each new strand

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2
Q

How is DNA replicated?

A

DNA replication is semiconservative

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3
Q

What is semiconservative in DNA replication

A

It is where each parent strand acts as a template for synthesis of a new strand where two replicated DNA molecule each contain one parent strand and one newly synthesized strand

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4
Q

Leading Strand

A

is synthesized continuously

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5
Q

Lagging Strand

A

Is synthesized in pieces called Okazaki fragments held together by ligase

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6
Q

Ligase

A

The enzymatic glue that holds Okazaki fragments

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7
Q

Origin of Replication (ori)

A

Is the place where the pre-replication complex binds. Binding occurs when proteins in the complex recognize specific DNA sequences within the ori

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8
Q

Chargaff’s Rule

A

Is the amount of adenine = the amount of thymine and the amount of guanine = the amount of cytosine

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9
Q

Why are mutation rates so much lower than expected?

A

DNA polymerase has proofreading capabilities and mismatched-repair occur

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10
Q

How does DNA polymerase replicates DNA?

A

It replicates it by adding nucleotides only to the 3’ end of each growing strand

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11
Q

New synthesized DNA goes in what direction?

A

It goes in the 5’ to 3’ direction

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12
Q

DNA Proofreading

A

It occurs right after DNA polymerase inserts a nucleotide.

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13
Q

Mismatch Repair

A

Occurs after DNA has been replicated and is a second set of proteins surveys the newly replicated molecule

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14
Q

What does DNA proofreading do?

A

When a DNA polymerase recognizes a mispairing of bases, it removes the improperly introduced nucleotide and tries again

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15
Q

What does mismatch repair do?

A

It looks for mismatched base pairs that were missed in proofreading and removes the incorrect nucleotides and then has DNA polymerase insert the correct sequence

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16
Q

Mutations

A

Are changes in the nucleotide of sequence of DNA that are passed on from one cell or organism to another. It may or may not affect the phenotype

17
Q

What are the two types of mutations?

A

Somatic mutations

Germline mutation

18
Q

Somatic Mutation

A

It occur in the somatic (body) cells of a multicellular organism that are passed onto the daughter cells during mitosis and in turn to the offspring of those cells. These mutations are not passed on to gametes

19
Q

Germline Mutation

A

It occurs in the cells of the germ line - the specialized cells that give rise to gametes and gametes with this mutation will pass it on to a new organism at fertilization

20
Q

Silent Mutation

A

They do not affect gene function and are mutations in DNA that are not expressed or mutations within an expressed region that do not have any effect on the encoded protein. Most mutations in large genomes are silent

21
Q

Loss of Function Mutation

A

It can result in either the loss of expression of a gene or in the production of a nonfunctional protein or RNA (usually seen in recessive inheritance)

22
Q

Gain of Function Mutation

A

It leads to a protein with an altered function and usually shows dominant inheritance and is common in cancer

23
Q

Conditional Mutation

A

This causes their phenotypes only under certain restrictive condition (usually under temperature)

24
Q

Miessence Mutation (Single point Mutation)

A

Is the addition or subtraction of a single nucleotide base that results in an altered phenotype or creates different amino acid

25
Q

Chromosomal Mutation

A

They are extensive and they change the position or cause a DNA segment to be duplicated or lost

26
Q

Deletion mutation of chromosomes

A

It is the removal of part of the genetic material and the consequences can be severe or even fatal

27
Q

Duplication mutation of the chromosome

A

It can be produced at the same time as deletions and would arise if homologous chromosomes broke at different positions and then reconnect with the wrong partners.

28
Q

Inversion mutation of the Chromosome

A

Is the result of breaking and rejoining chromosomes by removing a segment of DNA and reinsert it into the same location of the chromosome that’s in the wrong direction

29
Q

Translocation mutation of the chromosome

A

Results when segments of chromosomes break off and become joined to different chromosomes

30
Q

What are the benefits of Mutations?

A
  1. May cause an advantageous change in offspring

2. May provide the raw material for evolution in the form of genetic diversity