Chromosomes And Protiens Flashcards

1
Q

In what type of cells does splicing occur to pre-mRNA

A

Eukaryotic cells

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2
Q

What is the role of DNA helicase in transcription

A

Break hydrogen bonds in DNA molecule

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3
Q

what joins to the DNA template strand during transcription

A

Free RNA nucleotides in the nucleus join there complementary base pair on the template strand and form hydrogen bonds

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4
Q

What enzymes catalyses the formation of phophodiester bonds between the RNA nucleotides in transcription

A

RNA polymerase

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5
Q

When does transcription stop

A

When a stop codon is reached

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6
Q

What does pre-mRNA do with the template strand in transcription?and why ?

A

Dissociâtes from the DNA template strand because of the instability.
Therefore the hydrogen bonds are broken

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7
Q

What is splicing?

A

The removal of introns from pre-mRNA

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8
Q

What is a pre-mRNA strand made up of

A

Introns and exons

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9
Q

What is an intron

A

A non coding section of a pre-mRNA strand

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10
Q

What is a codon

A

A coding section of a pre-mRNA strand

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11
Q

Name a disease caused by incorrect splicing

A

Cistic fibrosis

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12
Q

What organelle is involved in the process of translation during protein synthesis

A

Ribosomes

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13
Q

What is free floating in the cytoplasm that attaches to the ribosome with complementary bases in translation

A

tRNA

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14
Q

What on the tRNA molecule is complementary to the mRNA

A

The anticodon

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15
Q

What does a tRNA molecule carry

A

A specific amino acid

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16
Q

What is used to hydrolyse the bonds between two amino acids in translation

A

ATP
An enzyme

17
Q

What bond forms between amino acids

A

Peptide bonds

18
Q

When does the ribosome stop doing translation

A

When a stop codon is reached

19
Q

What is formed during translation

A

A polypeptide chain of amino acids
The primary structure of a protein

20
Q

Define mutation

A

A change within the DNA usually the sequence or quantity of the nitrogenous bases

21
Q

What causes mutations

A
  1. Natural copying errors
  2. Exposure to mutagens
22
Q

What is a mutagen

A

A chemical or physical agent that is capable of inducing change in DNA known as mutations

23
Q

What is a substitution mutation

A

When one nucleotide is replaced by another nucleotide which will change the base within the triplet that codes for an amino acid 

24
Q

What is a silent mutation

A

When a change in base has no impact on the sequence of amino acids in the polypeptide chain 

25
Why do silent mutations occur?
 the DNA code is degenerate
26
What is a missense mutation?
When a change in the base causes a change in the amino acid that the triplet codon codes for which could change the overall 3D tertiary structure of the protein altering its function
27
What is a nonsense, mutation
When a change in the nucleotide changes, the nitrogenous base, so therefore causes the amino acid to change. In this case it is a stop code on and makes the protein completely non-functional.
28
What is a deletion mutation?
When one nitrogenous base is completely removed, which completely changes the triplet codon
29
What is the name given to what happens when a deletion mutation occurs?
Frame shift
30
What is a nondisjunction mutation?
When the chromosomes fail to separate during meiosis, which causes the gametes to have one more or one less chromosome E.g. down syndrome
31
What are the benefits of mutations?
It produces genetic diversity It helps with natural selection It has helped with evolution
32
What are the disadvantages of mutation?
Most mutations produced organisms that are less suited to the environment 
33
Give some features of prokaryotic DNA
Found in the cytoplasm of bacteria The DNA is circular and non linear It is not associated with proteins / histones It does not contain introns (non coding sections) Shorter than eukaryotic DNA