Module 4: Nucleic Acid And Protein Synthesis And Their Regulation Flashcards

1
Q

How are the proteins and nucleic acids of a cell produced and maintained?

A

4 basic genetic processes that help: protein synthesis, DNA replication, DNA repair, and genetic recombination

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2
Q

Why do cells need proteins?

A

Proteins are extremely important for the minute-by-minute, day-by-day functions of all cells

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3
Q

What steps are involved in protein synthesis?

A

Includes DNA transcription, mRNA translation, ribosomal assembly

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4
Q

Transcription

A

First step in protein synthesis
Takes the genetic info from DNA and transcribes it into the form of mRNA → the immature mRNA is modified by RNA splicing to remove its introns (non-coding regions)
Done by the enzyme RNA polymerase

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5
Q

RNA polymerase in transcription

A

Can recognize a promoter sequence in DNA → binds to this sequence with the help of transcription factors → then initiate the transcription of the downstream genes
Once it reaches the termination sequence → dissociates from the template DNA strand → releases the newly synthesized immature mRNA to be modified by splicing

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6
Q

Methods of gene expression

A

Gene regulatory protein
Histone acetylation and deacetylation
Methylation

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7
Q

Types of RNA involved in protein synthesis

A

mRNA
rRNA
tRNA

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8
Q

rRNA aka ribosomal RNA

A

Makes up the structure of the ribosome

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9
Q

Role of the ribosome in protein synthesis

A

Ribosome= the enzyme that catalyzes the formation of peptide bonds in a protein

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10
Q

Peptide bonds

A

Connections between each amino acid

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11
Q

tRNA aka transfer RNA

A

The RNA that carries specific amino acids based on the genetic code to the ribosome that then creates peptide

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12
Q

How does the tRNA know which amino acid it needs to take to the ribosome to make protein?

A

It contains an anticodon → used when a tRNA transfers an amino acid corresponding to the genetic code → it tells the tRNA which amino acid is next in the polypeptide sequence

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13
Q

Codons in the DNA

A

Are 3-nucleotide sequences that correspond to specific amino acids
A group of 3 nucleotides = a reading frame → when protein synthesis occurs, the DNA code is read by 3 nucleotides

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14
Q

Anticodon

A

Complementary to the codon present in DNA
Tells the tRNA which amino acid is next in the polypeptide sequence

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15
Q

Prokaryotic ribosomes vs. Eukaryotic ribosomes

A

Prokaryotes and eukaryotes have different ribosomes
Prokaryotes → the 70S ribosome = made of a 30S and a 50S subunit
Eukaryotes → the 80S ribosome = made of a 40S and a 60S subunit

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16
Q

Structure of ribosomes

A

All ribosomes have an A site, a P site, and an E site
A site = part where the tRNA delivers the amino acid
P site = part where the formation of the peptide bond is catalyzed
E site = where the peptide chain exits the ribosome as it’s being synthesized

17
Q

Stop codons

A

Three codons within the code thatcorrespond to the stoppage of translation
They are UAG, UAA, and UGA

18
Q

Start codon

A

A codon that signals the start of translation
It is AUG → corresponds to the amino acid methionine
Prokaryotes → this amino acid has a formyl group attached = fMet/ formyl-methionine

19
Q

Codons corresponding to the 20 essential amino acids

A

UUU, UUC = Phe
UUA, UUG, CUU, CUC, CUA, CUG =Leu
UCU, UCC, UCA, UCG =Ser
UAU, UAC = Tyr
UAA, UAG, UGA =STOP
UGU, UGC =Trp

20
Q

DNA repair mechanisms

A

The cells use these to maintain DNA in its optimal state → to fix lesions in DNA that may occur spontaneously or through exposure to harmful substances

21
Q

Mutations in DNA

A

Constantly occur spontaneously
Can be disease-causing or not
Cells try to repair but if not repaired, they can get passed throughout generations
Natural selection usually eliminates disease-causing mutations → only present at low rates
Different types: point mutations, frameshift mutations

22
Q

Point mutations

A

Caused by a single base pair change
Includes silent, missense, and nonsense mutations

23
Q

Frameshift mutations

A

Result in a shift in the reading frame → causes production of a short (truncated) protein or can add the wrong amino acid, changing the protein structure entirely

24
Q

Common types of DNA repair mechanisms

A

Base excision repair, double-stranded break repair, and mismatch repair

25
Q

Base excision repair

A

Only the damage nucleotide is removed and then replaced
Everything is then glued back together using the enzyme DNA ligase → like a hot glue gun

26
Q

Mismatch repair

A

Mis-paired buses are removed from the DNA strand
1. A number of proteins recognize the mismatched area →2. They cut out that whole patch of DNA → 3. DNA polymerase puts in the new and correct bases → 4. DNA ligase glues the pieces back together

27
Q

Double-stranded break repair

A

Used when DNA has been damaged and a double-stranded break was created
This type of damage can occur when exposed to high-energy radiation or other factors
This repair is done via 2 mechanisms: non-homologous end joining (NHEJ) and homologous recombination (HR)

28
Q

Non-homologous end joining (NHEJ)

A

The DNA is just glued back together at the breakage point
Not the best repair method → the cell can lose some DNA or have an addition of DNA at the breakage point
Result = usually a small mutation at the breakage site

29
Q

Homologous recombination (HR)

A

The information of the damaged chromosome is found in the homologous sister chromosome/chromatid → this info is used to repair the DNA