Transcription and Translation, Mutation Quiz Flashcards

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1
Q

The central dogma

A

Fundamental principle of molecular genetics

-States that genetic information flows from DNA→RNA→proteins

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2
Q

RNA Vs DNA

A

DNA:
Sugar: DNA contains deoxyribose, a sugar with one less oxygen atom than ribose.
Strands: DNA is typically double-stranded, forming a double helix.
Bases: The four nitrogenous bases in DNA are adenine (A), thymine (T), cytosine (C), and guanine (G). Adenine pairs with thymine, and cytosine pairs with guanine.
Shape: The double-stranded structure is stable and coiled into a double helix.

RNA:
Sugar: RNA contains ribose, a sugar with one more oxygen atom than deoxyribose.
Strands: RNA is usually single-stranded.
Bases: RNA uses adenine (A), uracil (U), cytosine (C), and guanine (G). In RNA, uracil replaces thymine as the complementary base to adenine.
Shape: RNA is typically single-stranded and can fold into various shapes, depending on its function.

  1. Function
    DNA:
    Genetic Material: DNA stores the genetic instructions used in the growth, development, functioning, and reproduction of all living organisms. It is the blueprint for all biological information.
    Replication: DNA is replicated when cells divide, ensuring that each new cell receives an exact copy of the genetic information.

RNA:
Protein Synthesis: RNA plays a central role in protein synthesis.

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3
Q

Transcription - Initiation

A

initiation
Promoter region: a sequence of nucleotides in DNA that indicates where the RNA polymerase complex should bind to initiate transcription

-Key element of the promoter in eukaryotes is the TATA box (a portion of DNA with high percentage of Adenine and Thymine bases)

-Prokaryotes have a TATATT sequence instead for this

-RNA polymerase binds to a promoter region on the DNA same purpose

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4
Q

Transcription - Elongation

A

Elongation
RNA polymerase complex works its way along DNA molecule

-RNA polymerase, unlike DNA polymerase, can begin making the complementary copy without needing a primer to be already in place

-Synthesizes mRNA strand that is complementary to template strand of DNA

-T is replaced with U

-RNA polymerases work in the 5ʼ → 3ʼ direction, using the 3ʼ→ 5ʼ DNA strand as a template strand.

As RNA polymerase moves along the DNA, it unwinds the DNA at the forward end of the enzyme

-RNA strand grows as nucleotides are added, one by one forming a temporary RNA-DNA double helix with the template strand

-As the RNA polymerase passes, the DNA double helix reforms

-Once an RNA polymerase molecule has started transcription and progressed past the beginning of a gene, another molecule of RNA polymerase may start producing another RNA molecule if there is room at the promote

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5
Q

Transcription - Termination

A

The transcription is terminated when RNA polymerase recognizes a termination sequence.

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6
Q

Coding (sense) vs Template (anti-sense) strand

A

-Coding strand: the DNA strand that is not being copied but contains the same sequence as the new RNA molecule

-The template strand contains the sequence that is complementary to the sequence that is going to be transcribed

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7
Q

mRNA processing in eukaryotes (poly A tail, G cap, splicing of exons)

A

Poly(A) tail: a chain of adenine nucleotides added to the 3’ end of pre-mRNA molecule to protect it from enzymes in the cytosol

-Enables mRNA to be translated efficiently and protects from attack by RNA-digesting enzymes in the cytosol

The intron sequences are removed from pre-mRNA and exons are joined together to form mature mRNA

G Cap

-Involves covalent linkage of modified G nucleotides onto to 5’ end of pre-mRNA

-The cap is recognized by the protein synthesis machinery

-All eukaryotic mRNA undergo modifications on their ends

-These modifications convert precursors mRNA (pre-mRNA) to mature mRNA

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8
Q

Exons vs introns, alternate splicing

A

Exons are coding regions

Exons may be joined in different combinations to produce different mRNAs from a single DNA gene sequence
-A mechanism called alternative splicing increases number and variety of proteins encoded by a single gene

-Allows more than one possible polypeptide to be made from a single gene

-Alternative splicing helps understand why humans with only 20 000 genes can produce approx. 100 000 proteins

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9
Q

Structure tRNA

A

-3’ end of tRNA binds to specific amino acids

-Anticodon on tRNA complements mRNA codon

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10
Q

Structure of ribosome - a, p and e sites

A

-2 subunits: small and large

-E site → exit site

-P site → polypeptide binding site

-A site → amino acid site

-Composed of proteins and rRNA

-3 tRNA binding sites

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11
Q

Translation - Initiation

A

-mRNA, tRNA and small ribosomal subunit bind with P site at start codon

-Only the first tRNA binds to P at start codon

-Large subunit binds using energy from GTP

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12
Q

Translation - Elongation

A

mRNA read 3 nucleotides at a time in codons

-tRNA brings corresponding amino acid into the A site of the ribosome

-Ribosome catalyzes dehydration synthesis reaction between amino acids in P site and A site

-Peptide bond is formed

-Growing polypeptide now attached to tRNA in A site

-Ribosome moves forward one codon

-Free tRNA in P site exits out the back of ribosome on the E site

-tRNA (with polypeptide) moves into P site

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13
Q

Translation - Termination

A

-Elongation continues until reaching a stop codon

-There is no amino acid for stop codon, just STOP

-Release factor binds and hydrolyzes the bond between the last tRNA and its amino acid

-New protein is free

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14
Q

Frameshift Mutations

A

– shifts the reading frame of the codons so that a completely different amino acid sequence is produced from the point of the shift. Will likely not produce a functional protein

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15
Q

point mutations

A

– change in one nucleotide

○Substitution
○Substitutions will only affect a single codon
■THE FAT CAT ATE THE RAT
■THE FAT HAT ATE THE RAT
○Insertion (Frameshift)

■THE FAT CAT ATE THE RAT
■THE FAT CAT HATE THE RAT
○Deletion (Frameshift)

■THE FAT CAT ATE THE RAT
■THE FAT CAT AT THE RAT

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16
Q

Missense

A

A substitution that results in a different amino acid is
called a missense mutation

17
Q

Nonsense

A

A nonsense mutation produces a premature STOP codon

18
Q

Silent

A

If the mutation still produces the same amino acid it is
called a silent mutation. -Has no impact on the protein formed-This happens because the genetic code is degenerate