Genetic control of protein structure and function Flashcards

1
Q

What is transcription?

A

The formation of pre-mRNA molecules ,from the DNA that makes up a particular gene, which are then spliced to form mRNA, this is the first stage of protein synthesis

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2
Q

What is translation?

A

The mRNA formed during transcription is used as a template to which complementary tRNA molecules attach and the amino acids they carry are linked to form a polypeptide

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3
Q

What is DNA made up of?

A

Nucleotides that contain a deoxyribose sugar, phosphate group and a nitrogenous base (A,T,C or G)

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4
Q

How do the nucleotides join together to form polynucleotides?

A

By creating a sugar-phosphate backbone, a phosphate group of one nucleotide joins to the sugar of another

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5
Q

How do two DNA polynucleotide stands join?

A

Hydrogen bonding between the complimentary bases (A-T, C-G)

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6
Q

What are genes?

A

Sections of DNA that are found on chromosomes that code for a specific protein (polypeptide)

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7
Q

What are proteins made of?

A

Chains of amino acids

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8
Q

What determines the order of amino acids in a protein?

A

The order of nucleotide bases in a gene

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9
Q

What is meant by a triplet code?

A

A sequence of 3 bases (e.g. GTC=one amino acid) also known as a DNA /Base triplet or codon

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10
Q

Where Is DNA found in the cell?

A

Nucleus

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11
Q

What is the function of ribosomes and where are they found in the cell?

A

Protein synthesis and cytoplasm

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12
Q

What is RNA made up of?

A

Nucleotides of a ribose sugar, phosphate group and a base (A,U,C,G)

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13
Q

What is the different in structure of DNA and RNA?

A

DNA is a double stranded twisted helix whereas RNA is single stranded

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14
Q

What is mRNA used for and where is it made?

A

Carries the genetic code for the DNA in the nucleus to the cytoplasm, via a nucleic pore, where it’s used to make proteins during translation. It is made in the nucleus during transcription and is formed from pre-mRNA after it has been spliced to remove any introns (non-coding DNA)

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15
Q

What is an exon?

A

Coding section of DNA

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16
Q

What is the role of the enzyme DNA helicase during transcription?

A

It breaks the hydrogen bonds between the bases on a specific region of DNA, causing the two strands to separate and expose the nucleotide bases in that region

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17
Q

What is the function of the enzyme RNA polymerase during transcription?

A

Moves along one of the two DNA strands(template strand) causing the nucleotides on this strand to join with the individual complementary nucleotides free in the nucleus

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18
Q

How does RNA polymerase know when to stop transcribing the pre mRNA?

A

When it reaches a stop codon it stops making pre mRNA and detaches from the DNA

19
Q

How is pre-mRNA changed into mRNA?

A

Introns are removed via splicing , leaving the remaining exon sections to rejoin in a variety of differ erm combinations

20
Q

What happens to the mRNA after the splicing process?

A

It moves out of the nucleus via a nuclear pore and attaches to a ribosome in the cytoplasm, which marks the start of translation

21
Q

What is tRNA and what is its function?

A

A single polynucleotide strand folded into a clover shape in which hydrogen bonds between specific base pairs hold the molecule in this shape. It is involved in translation and carries the amino acids that are used to make proteins to the ribosome

22
Q

How can a tRNA molecule carry an amino acid?

A

Each molecule had a specific sequence of 3 bases at one end called an anti codon, and have an amino acid binding site at the other end

23
Q

Where is tRNA found?

A

Cytoplasm of cells

24
Q

What are the different in bases in DNA and RNA?

A

DNA contains A,T,C,G whereas RNA contains A,U,C,G

25
Q

Where does transcription occur?

A

Nucleus

26
Q

Where does translation occur?

A

At ribosomes in the cytoplasm

27
Q

What is an anticodon?

A

A sequence of 3 adjacent nucleotides on a molecule on tRNA that is complimentary to a particular codon on a mRNA molecule

28
Q

What are the stages of translation?

A
#  Ribosome attaches itself to the starting codon at one end of the mRNA
# Complementary tRNA molecule pairs up with the sequence on mRNA via it's anticodon, and carries a specific amino acid
#A tRNA with a complementary anticodon pairs up with next codon on mRNA, carrying another amino acid
#Amino acids joined together by peptide bonds
#First tRNA molecule detaches itself from it's amino acid
# Ribosome moves along mRNA by one codon
#Continues to move along mRNA until it reaches a stop codon
#Polypeptide chain is released and folded into it's correct shape
29
Q

What is meant by a mutation?

A

A change in the sequence of bases in DNA, which could result in a change to the quantity or structure

30
Q

When are mutations passed on to the next generation?

A

If they occur in the gametes (sex cells)

31
Q

What is meant by a gene mutation?

A

Any change to one or more nucleotide bases/rearrangement of bases in DNA

32
Q

What is substitution?

A

The type of gene mutation in which a nucleotide in DNA is replaced by another nucleotide with a different base

33
Q

What are the 3 types of substitution?

A

Nonsense, mis-sense and silent mutations

34
Q

What is a nonsense mutation?

A

When the base change results in the formation of a stop codon, marking the end of a polypeptide chain which may lead to a non-function protein

35
Q

What is a mis-sense mutation?

A

When the base change results in a different amino acid being coded for

36
Q

What is a silent mutation?

A

When the substituted base still codes for the same amino acid before, due to the degenerate nature of the genetic code

37
Q

Why is the genetic code known as being degenerated?

A

Amino acids have more than one codons that code for them e.g. GTC and GTT both code for glutamine

38
Q

What is deletion?

A

When a nucleotide is lost from a DNA sequence, creating a frame shift. If they occur at the start of a sequence, they will have a huge effect as an entirely different protein may be translated, or it may be non-functioning

39
Q

What is meant by a frame-shift?

A

When the reading frame that contains each 3 letters of the code has been shifted to the left by one letter e.g.

T G C A G G TAC
Removal of guanine from first codon

40
Q

What are the causes of mutations?

A
  • Can occur spontaneously during an error in DNA replication
  • Genetic inheritance
  • Mutagenic agents: High energy radiation (e.g. UV) and chemicals (e.g. tar)
41
Q

Which genes are responsible for the control of cell division?

A

Proto-oncogenes and tumour suppressor genes

42
Q

What is the role of proto-oncogenes?

A

They stimulate cell division (can cause tumour or cancer to develop) They may be mutated into oncogenes which can affect cell division by:

  • Permanently activating receptor protein on CSM so cell division occurs even without growth factors
  • They may code for a growth factor that is then produced in excessive amounts
43
Q

What is the role of tumour suppressor genes?

A

They slow down cell division (opposite to proto-oncogenes) It maintains the normal rate of cell division and prevents tumour formation

44
Q

What happens if a tumour suppressor gene is mutated?

A

Becomes inactivated, meaning it stops inhibiting cell division and allows the rate of it to increase