Lecture 6- Regulation of Gene expression Flashcards

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1
Q

structure of a gene

A

-contains a promoter, coding sequence, and a terminator

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2
Q

Within the promoter

A
  • is the controlling site

- where induction (increased expression of a gene) occurs

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3
Q

Operon

A

-regulates genes
-one promoter serving several genes
ex- typtophan and lactose

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4
Q

Operator

A
  • the operon’s switch for controlling transcription
  • where the repressor binds
  • determines whether RNA polymerase binds to the promoter and produces proteins or not
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5
Q

Repressor

A
  • switches the operon off
  • blocks attachment of RNA polymerase, therefore blocks transcription
  • is specific
  • is allosteric: 2 different shapes, active and inactive
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6
Q

co-repressor

A

molecule that binds to repressor to switch an operon off

-tryptophan

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7
Q

Tryptophan absent

A
  • RNA polymerase binds to promoter
  • transcribes mRNA to make more tryptophan
  • operon on, repressor off
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8
Q

Tryptophan present

A

a lot of tryptophan-> tryptophan acts as a co-repressor

  • tryptophan binds to repressor and activates it
  • repressor attaches to operator
  • RNA polymerase can no longer transcribe
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9
Q

Tryptophan operon

A
  • example of repressible operon

- turned off by the end product of metabolic pathway

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10
Q

Lactose operon

A
  • example of an inducible operon
  • usually inactive
  • can be turned on by the precursor/first chemical of the metabolic pathway
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11
Q

Lactose not present

A
  • repressor binds to operator and blocks RNA polymerase

- mRNA cannot be made and proteins/enzymes cannot be made

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12
Q

Lactose present

A
  • lactose binds to repressor, changing repressor’s shape and making it unable to bind to operator
  • RNA polymerase binds to promoter and transcribes to make mRNA
  • mRNA is used to make the enzymes that break down lactose
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13
Q

Regulatory genes

A
  • codes for production of allosteric repressor protein that can switch off operon
  • ex: lacI
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14
Q

Structural genes

A

ex- the enzymes for lactose, break down lactose

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15
Q

Mutations

A
  • a permanent change in DNA

- source of new genes

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16
Q

Mutagens

A
-physical and chemical agents that promote mutations
ex:
-ionizing radiation
-ultraviolet radiation
-chemical mutagens 
-pyrimidine dimer
-spontaneous mutations
17
Q

Point mutation

A
  • change in single nucleotide pair of a gene
  • change of a single nucleotide in the DNA’s TEMPLATE STRAND leads to altered mRNA and abnormal protein
  • some have no effect on the encoded protein due to the redundancy of the genetic code
18
Q

Silent mutation

A
  • no effect on amino acid sequence

- no observable effect on phenotype

19
Q

Missense mutation

A
  • changes one amino acid

- may have little effect, or big effect

20
Q

Nonsense mutation

A
  • causes translation to be ended early

- leads to a non functional protein

21
Q

Insertion

A

additions of nucleotide pairs in a gene

22
Q

Deletions

A

removal of nucleotide pairs in a gene

23
Q

Insertions and Deletions

A

both alter the reading frame of mRNA

-more disastrous effect

24
Q

Frame-shift mutation

A
  • when insertion/deletion is not a multiple of three
  • results in extreme missense mutations
  • non functional protein