Lecture 12 Flashcards

1
Q

Unidirectional

A

Information can only go in one direction

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2
Q

Gene

A

A region of DNA that is transcribed and has a function in the cell

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3
Q

Promoter

A

Site of RNA polymerase assembly, DNA sequence that determines start of gene, no promoter means no gene

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4
Q

TATA Box

A

AT rich sequence found 10 base pairs before transcription start

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5
Q

Transcription Factors

A

Proteins that recognize and bind the TATA box, can read DNA, recruits RNA polymerase because RNA pol can’t identify promoter on its own

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6
Q

Transcription

A

DNA to mRNA

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7
Q

Template Strand

A

Used in transcription, runs 3’ to 5’ away from promoter

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8
Q

Coding Strand

A

Complementary and antiparallel to template, runs 5’ to 3’ away from promoter, not used in transcription

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9
Q

Transcript

A

mRNA product

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10
Q

RNA Polymerase

A

Enzyme of transcription, part of a transcription initiation complex that assembles at the promoter, can open DNA into a transcription bubble

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11
Q

UTR

A

Untranslated region, space on RNA either before translation start or after translation stop

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12
Q

Elongation

A

Occurs where RNA polymerase add nucleotides 5’ to 3’ and transcript is released out of complex

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13
Q

Post-transcriptional Processing

A

Eukaryotes only, occurs in nucleus, increase stability of transcript

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14
Q

meG Cap

A

Methylguanosine cap, modified base, forms a 5’ to 5’ linkage with eukaryotic mRNA to hide 5’ end from exonuclease digestion

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15
Q

PolyA Tail

A

Added to 3’ end of eukaryotic mRNA, delays exonuclease digestion and aids in translation initiation.

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16
Q

RNA Splicing

A

Removal of intervening sequences from coding region (introns)

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17
Q

Introns

A

Non-amino acid coding regions which contain intervening sequences found in a eukaryotes gene’s DNA but not in the mature mRNA

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18
Q

Exons

A

Amino acid coding regions which contain expressed sequences found in both a eukaryotes gene’s DNA and in the mature mRNA

19
Q

Spliceosome

A

Complex of snRNPs, enzyme of splicing

20
Q

snRNPs

A

Protein/RNA complexes (quaternary structure) which recognize sequences at intron/exon boundaries

21
Q

Alternative Splicing

A

Mixing and matching of exons, makes similar but not identical proteins from same gene

22
Q

Translation

A

RNA to Protein

23
Q

Codon

A

3 nucleotides associated with an amino acid

24
Q

tRNA

A

Transfer RNA, functional RNA, amino acid binding region and mRNA base pairing region (anticodon), carries appropriate amino acid to ribosome

25
Anticodon
Antiparallel and complementary to mRNA codon
26
Aminoacyl tRNA Synthetase
Enzyme that pairs correct amino acid based on anticodon sequence, covalently links amino acid to tRNA, energy from ATP hydrolysis
27
Ribosomes
Catalyze peptide bonds
28
Large Ribosomal Subunit
Contains rRNA and catalytic site
29
Small Ribosomal Subunit
Contains rRNA and recognizes and binds RBS (reads mRNA)
30
RBS
Ribosomal binding site, prokaryote only, sequence in mRNA that is recognized by base pairing with rRNA in small ribosomal subunit
31
Formyl-methionine
Modified amino acid, unique to prokaryotes, first amino acid of protein synthesis (found on amino terminal)
32
Bind
Charged tRNA approaches A site and binds to the mRNA (anticodon-codon base pairing)
33
Bond
Peptide bond forms between amino acid chain attached to tRNA 1 and amino acid on tRNA 2, peptide chain transfers to tRNA 2
34
Shift
Ribosome shifts down that mRNA (towards 3’ end) in a 1 codon step
35
Mutagens
Mutation causing factors
36
Mutations
Changes to sequence in DNA
37
Base-pair Substitution
Mutation at the DNA level, replacement of one nucleotide and its partner with another pair
38
Silent Mutation
Mutation at the protein level, no change in primary amino acid sequence due to redundancy in genetic code
39
Missense Mutation
Mutation at the protein level, encodes the wrong amino acid, MAY affect protein function
40
Nonsense Mutation
Mutation at the protein level, premature stop codon, shortened protein, may affect protein structure
41
Frameshift Mutation
Mutation at the protein level, single base pair addition or deletion that changes the reading frame of a protein
42
Spontaneous Mutation
Error in copying of DNA sequence
43
Induced Mutation
Exposure to mutagens