gene expression Flashcards

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1
Q

DNA –> (____) –> RNA –> (____) –> protein/polypeptide

A

DNA –> (transcription) –> RNA –> (translation) –> protein/polypeptide

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2
Q

DNA occurs in the _____ of the ______. While some RNA also occur in the ____, most is found in the _____, particularly in the _____.

A

DNA occurs in the chromosomes of the nucleus. While some RNA also occur in the nucleus, most is found in the cytoplasm, particularly in the ribosomes.

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3
Q

3 types of RNA?

A

Messenger RNA (mRNA) - transfer information from nucleus to cytoplasm
Transfer RNA (tRNA) - construction of proteins at ribosomes in the cytoplasm
Ribosomal RNA (rRNA) - forms structural and functional components of ribosomes

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4
Q

The role of DNA is to instruct the cell to make specific ________.

A

The role of DNA is to instruct the cell to make specific polypeptides and proteins.

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5
Q

How is DNA, genes, chromosomes related?

A

The huge length of DNA molecule is a single chromosome that carries the codes for a very large number of polypeptides. Within this extremely long molecule, the relatively short length of DNA that codes for a single polypeptide is called a gene.

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6
Q

The DNA triplet code is a ___ base / triplet code. Each triplet code codes for one ____ ____.

A

The DNA triplet code is a three base / triplet code. Each triplet code codes for one amino acid.

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7
Q

What determines the unique properties of each protein?

A
  • Which amino acids are involved in its construction
  • The sequence in which these amino acids are joined
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8
Q

What are the three stages of protein synthesis?

A
  1. Transcription - transfer of genetic information from DNA into an RNA molecule
  2. Amino acid activation (nothing much)
  3. Translation - transfer of information from RNA into a protein
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9
Q

Describe transcription.

A
  • Transcription occurs in the nucleus
  • A complementary copy of the code is made by building a molecule of mRNA
  • DNA triplet codes are transcribed into codons in mRNA
  • Catalysed by RNA polymerase: stupid enzyme (5’ –> 3’)
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10
Q

Name the first step of transcription and describe the process.

A

Initiation.
- Double helix unwinds and the hydrogen bonds are broken at the site of the gene being transcribed
- RNA polymerase recognises and binds to a “start” signal”, a nucleotide sequence called a promoter located at the beginning of a gene

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11
Q

Name the second step of transcription and describe the process.

A

Elongation.
- The template strand (3’ –> 5’) is used as the template for transcription
- RNA polymerase matches free nucleotides by complementary base pairing, working in the 5’ –> 3’ direction
- Hydrogen bonds then form between complementary bases. Each free nucleotide is then joined by a condensation reaction between the sugar + phosphate groups of adjacent nucleotides on the DNA strand

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12
Q

Name the third step of transcription and describe the process.

A

Termination.
- When RNA polymerase reaches a special sequence called a terminator, on the template strand, transcription is terminated and the mRNA is released.
- It leaves the nucleus through pores in the nuclear envelope and passes to ribosomes in the cytoplasm.

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13
Q

If you are given the coding strand how do you figure out the mRNA sequence?

A

COPY! But change the “T” to “U”

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14
Q

Describe amino acid activation.

A
  • Amino acid activation occurs in the cytoplasm.
  • Amino acids are activated by combining with transfer RNA (tRNA)
  • At one end of each tRNA is a site where an amino acid is attached. The another end is folded into a loop with an anticodon (complementary to the codon of mRNA that codes for the specific amino acid)
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15
Q

Name and describe the first step of translation

A

Initiation.
- On arrival at the ribosome, the mRNA binds to the small subunit at an attachment site. There are 6 bases (2 codons) of the mRNA exposed to the large subunit at any time.
- The first three exposed bases are always start codon AUG. A molecule of tRNA with the complementary anticodon UAC forms hydrogen bonds with this codon. Amino acid is attached to this tRNA molecule.

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16
Q

Name and describe the second step of translation

A

Elongation.
- A second tRNA bonds with the next three bases of the mRNA, bringing another amino acid
- Ribosome holds the two amino acids close together and a condensation reaction forms a peptide bond (catalysed by an enzyme found in large subunit). A dipeptide is formed
- The ribosome moves along the mRNA in the 5’ –> 3’ direction and the next codon is read. The first tRNA (WITHOUT the amino acid) leaves the ribosome.
- By these steps constantly repeated, a polypeptide is formed and emerges from the large subunit.

17
Q

Name and describe the third step of translation

A

Termination.
- Eventually, a “stop” codon is reached. At this point, the completed polypeptide is released from the ribosome into the cytoplasm.
- It is common for several ribosomes to move along the mRNA at one time. The structure is called a a polysome (mRNA, ribosomes and their growing protein chains)

18
Q

What are the three types of mutagens? How do they affect DNA?

A

Mutagens alter the DNA sequence of the cell.
Chemical mutagens (e.g. ethidium bromide): block DNA replication, resulting in a shorter DNA synthesised
Physical mutagens (e.g. X-rays, UV rays): damage DNA by breaking it into smaller fragments
Biological mutagens (e.g. HPV): inserts DNA into chromosomes of human cell, thereby altering the DNA sequence and disrupting gene functions

19
Q

What are the types of gene mutations?

A

Point mutation/nucleotide substitution (replacement of 1 nucleotide)
Nucleotide deletions/insertions (loss or addition of one or more nucleotides)

20
Q

How to answer questions for missense mutation?

A

EXAMPLE: There is a point mutation at the 13th nucleotide from C to T. This missense mutation alters the 5th codon CGC to UGC, hence producing an altered amino acid CYS instead of ARG. Hence, a non-functional protein is produced, human cationic trypsinogen gene.

21
Q

How to answer questions for nonsense mutation?

A

EXAMPLE: There is a point mutation at the 7th nucleotide from C to T. This nonsense mutation alters the 3rd codon CGA to UGA, which results in a premature “stop” codon UGA instead of ARG and an altered amino acid is produced. Translation of the messenger RNA transcribed from this mutant gene will stop prematurely, resulting in a truncated non-functional neurofibrumin.

22
Q

How to answer questions for insertion?

A

There is an insertion of 345 base pairs. Within these extra 345 base pairs is a premature stop codon UGA at 688th-690th nucleotides. Therefore, translation of the messenger RNA transcribed from this mutant gene will stop prematurely, resulting in a truncated non-functional dihydroflavonol 4-reductase.

23
Q

What are silent mutations?

A

They are a result of nucleotide substitution. Since genetic code is degenerate, even when the base of a codon is changed, the same amino acid can still be encoded, such mutations are said to be silent as they do not cause a change in their resulting polypeptide sequence and proper folding of the protein can still occur.