dna Flashcards

1
Q

charged amino acid

A

glutamic acid

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2
Q

3 types of substitutions mutations

A
  1. silent - no change in aa code
  2. missense - still code for an amino acid, but not necessarily the right one
  3. nonsense - change an amino acid codon into a stop codon
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3
Q

what are insertions or deletions

A

additions or losses of nucleotide pairs in a gene
- have a disastrous effect on the resulting protein more often than substitutions
- may alter the reading frame, producing a frameshift mutation

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4
Q

control of gene expression in prokaryotes

A

operons = A cluster of functionally related genes can be under coordinated control by a single on-off “switch” - the switch = OPERATOR - generally found within promoter

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5
Q

2 types of regulation of gene expression in prokaryotes

A

positive and negative

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6
Q

whats negative regulation of gene expression

A

uses 2 types of repressors that block RNA polymerase
- repressible - usually on (trp operon)
- inducible - usually off (lac operon)

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7
Q

repressible type of repressor

A

e.g. trp operon
- generally on
- anabolic metabolism
- compressor helper - tryptophan

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8
Q

whats in every lactose

A

1,6 allolactose

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9
Q

inducible type of repressor

A

e.g. lac operon
- generally off
- catabolic metabolism
- inducer helper - allolactose

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10
Q

whats positive regulation of gene expression in prokaryotes

A
  • CAP) = an activator of transcription - stimulatory protein
  • When glucose is scarce, CAP is activated by binding with cyclic AMP
  • Activated CAP attaches to the promoter of the lac operon + increases the affinity of RNA polymerase, thus accelerating transcription
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11
Q

what happens when glucose levels are low

A

cyclic AMP levels are high - high levels of transcription

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12
Q

what happens when glucose levels are high

A

cyclic AMP levels are low - low levels of transcription

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13
Q

DNA organization

A

DNA -> HISTONES -> NUCLEOSOMES -> CHROMATIN

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14
Q

control of gene expression in eukaryotes

A
  • regulation of chromatin structure
  • histone modification
  • DNA methylation
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15
Q

regulation of chromatin structures

A
  • genes can be packed into EUCHROMATIN (open / on) + HETEROCHROMATIN (closed / off)
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16
Q

histone modifications

A
  • histone acetylation: acetyl groups are attached to positively charged lysines in histone tails - loosens chromatin structure - promotes initiation of transcription
  • methylation: addition of methyl groups can condense chromatin
  • phosphorylation: addition of phosphate groups next to a methylated amino acid can loosen chromatin
  • HISTONE CODE HYPOTHESIS - specific combinations of modifications help determine chromatin configuration and influence transcription
17
Q

DNA methylation

A

add methyl groups to certain C bases
- can cause long-term inactivation of genes
- it is transgenerational

18
Q

regulation of transcription initiation

A

CONTROL ELEMENTS = segments of non-coding DNA that bind transcription factors
- ENHANCERS = may be far away from a gene or even located in an intron
- PROXIMAL CONTROL ELEMENTS = located close to the promoter
- activator - binds to an enhancer and stimulates transcription of a gene
- repressors - inhibiting expression of a particular gene

19
Q

Combinatorial control of gene activation

A
20
Q

mechanisms of post transcriptional gene regulation

A

allow a cell to fine-tune gene expression rapidly in response to environmental changes e.g. Gcap, splicing, mRNA degradation (mRNA can exist in the cytoplasm for long time)

21
Q

imitation of translation

A

mRNAs can be blocked by:
- RNA structure
- proteins
- other RNAs

22
Q

protein processing and degradation

A

After translation, various types of protein processing e.g. cleavage + the addition of chemical groups, are subject to control
- PROTEASOMES = giant complexes that bind protein molecules and degrade them

23
Q

2 types of RNAs that alter gene expression

A
  • Micro RNAs (miRNAs) - bind to mRNA and degrade it / block its translation
  • Small intefering RNAs (siRNAs) - bind to chromatin - form heterochromatin