3/18 regulation continued Flashcards

1
Q

when do we need to stop the trp operon?

A

when there are high levels or trptophan

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2
Q

is the trp operon anabolic or catabolic

A

it is anabolic, it makes trptophan

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3
Q

what are the two types of mechanisms for regulation of the trp operon?

A

the repression with a repressor protein and the formation of attenuating stem loops in the leader regions

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4
Q

what is the leader region

A

it is a sequence in the trp operon that contains an attenuator sequence

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5
Q

does the leader region encode for a polypeptide

A

no it does not

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6
Q

when the ribosome does not jump on to the DNA before transcription begins in the trp operon, what will occur?

A

the early terminator stem loop will form and attenuate the RNA polymerase

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7
Q

when there are high levels of trptophan, how is the trp operon affected?

A

high levels of trptophan correspond to high amounts of charged tRNAs. the ribosome will be able to move through the trp codons quickly and cause the formation of an early terminator which will attenuate transcription

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8
Q

when there are low levels of trptophan, how is the trp operon affected

A

low levels of trptophan correspond to low amounts of charged tRNAs. The ribosome will stall on the trp codons and cause the formation of an alternative loops that will allow transcription to continue

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9
Q

operons in catabolic processes will be

A

inducible (turned on)

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10
Q

in catabolic procsses, what typically acts as an inducer?

A

the substance to be broken down typically acts as the inducer

ex) allolactose

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11
Q

operons involved in anabolic processes are

A

repressible (shut off)

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12
Q

in anabolic processes, what acts as the inhibitor/corepressor

A

the product of the operon acts as the inhibitor/corepressor

ex) trptophan

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13
Q

provide an example of post-transcriptional regulation

A

anti-sense RNA

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14
Q

what is anti-sense RNA

A

it is a complementary strand of RNA that exists in the opposite direction of the sense strand and it will block translation by forming a double stranded RNA

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15
Q

how does translational regulation occur most commonly?

A

initiation of translation will be inhibited by regulatory proteins not allowing the ribosome to bind

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16
Q

what is direct translational regulation

A

the translational repressor binds next to the ribosome binding site or the start codon and this blocks the ribosome form binding

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17
Q

what is indirect translational regulation?

A

the regulatory protein will bind outside of the ribosome binding site or start codon and will stabilize a secondary mRNA structure that will prevent initiation

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18
Q

what is a riboswitch

A

it is an RNA that exists in two secondary conformations

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19
Q

what are the two conformations formed by a riboswitch?

A

an active conformation and an inactive one that inhibits gene expression

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20
Q

do riboswitches have anything to do with ribosomes?

A

no, they only refer to RNA

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21
Q

how do riboswitches work?

A

small molecules will bind to the RNA and cause a conformational change usually through a feedback mechanism

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22
Q

how does bacillus subtilis use a riboswitch

A

it utilizes riboswitches to trigger attenuation and stop transcription

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23
Q

For bacillus subtilis, how do low concentrations of TPP affect the riboswitch?

A

an anti terminator stem loop will form and transcription can continue

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24
Q

for bacillus subtilis, how do high concentrations of TPP affect the riboswitch?

A

TPP binds to the RNA and causes a conformation change where a terminator stem-loop will form and transcription will be attenuated

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25
Q

when do riboswitches occur in E-coli?

A

they occur in translation

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26
Q

for E. coli, how is the riboswitch affected when TPP concentrations are high

A

TPP acts as a feedback and will cause a stem-loop that blocks the ribosome binding site, ultimately inhibiting translation.

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27
Q

what is feedback inhibition?

A

it is a form of post-translational regulation where the final product in the enzymatic pathway will inhibit earlier enzymes to stop the process

28
Q

in feedback inhibition, how does the product interact with the initial enzyme

A

it binds allosterically with the enzyme at high concentrations and will change its conformation, ultimately turning it off

29
Q

what do low affinity binding sites depend on?

A

they depend on the concentration of the effector molecule. high concentrations result in better binding while low concentrations result in an unbound state

30
Q

in addition to feedback inhibition, what is the other form of postranslational regulation?

A

covalent modification of proteins to alter their structure and function

31
Q

what are three types of post translational covalent modifications that are reversible and alter the proteins function?

A

phosphorylation, acetylation, methylation

32
Q

why is gene regulation essential in eukaryotes?

A

genes need to be expressed at certain developmental periods and there are differences in cell types that may require different gene regulations

33
Q

what are the types of gene regulation in prokaryotes and eukaryotes

A

transcription, post-transcription, translation, post translation

34
Q

what are general transcription factors

A

proteins that are required for basal level transcription

35
Q

what transcription factors affect constitutive genes?

A

only general transcription factors, not regulatory

36
Q

where are general transcription factors always located?

A

next to the gene

37
Q

what are regulatory/specific transcription factors

A

they regulate the rate of transcription

38
Q

where are STFs located?

A

they are trans acting so they come from anywhere in cell, they can also act from far away

39
Q

what do regulatory transcription factors recognize?

A

they recognize cis regulatory elements located near the core promoter

40
Q

what do activator transcription factors bind to?

A

enhancer DNA binding elements to increase transcription

41
Q

what do repressor TFs bind to?

A

silencer DNA elements

42
Q

are activators and repressors always present in eukaryotes?

A

no, it depends when the cell needs them but they are not always present

43
Q

what is combinatorial control

A

ieukaryotic genes are regulated by a combination of factors

44
Q

why are nucleosomes relevant in eukaryotic gene regulation

A

the levels of compaction can affect transcription but this can be altered by regulatory proteins

45
Q

what are epigenetic modifications

A

they are reversible changes in gene expression that do not alter the DNA (chromatin structure)

46
Q

what is up regulation

A

it increases transcription by the binding of a TF to an enhancer

47
Q

what is down regulation

A

it decreases transcription due to the binding of a repressor to a silencer

48
Q

what does it mean for a DNA regulatory element to be bidirectional

A

they can regulate promoters that are up or downstream of the element

49
Q

response elements for specific transcription factors can be located:

A

anywhere and very far from the promoter

50
Q

True or false: regulatory transcription factors will directly interact with the core promoter

A

false, they can but not always

51
Q

how do TFs directly interact with the core promoter

A

they can directly interact with TFIID or through coactivators

52
Q

how does indirect transcription regulation occur?

A

through a mediator, the repressors will inhibit mediators while activators will stimulate them

53
Q

what are the three ways regulatory transcription factors are regulated

A

1) effector molecule binding
2) protein-protein interactions
3) covalent interactions

54
Q

how do effector molecules regulate TFs

A

they allosterically bind and induce conformational changes that enable their function

55
Q

what is a protein-protein interaction

A

it is a form of TF regulation, where two TFs of the same type (homo) or different (hetero) form dimers that enable them to access the major grooves of the DNA

56
Q

how does post translational modification of a TF enable transcription?

A

covalent modifications like phosphorylation can activate them into their roles

57
Q

for hormones like glucocorticord and gonadoticoids, how are they regulated?

A

by combinatorial factors

58
Q

true or false, transcription factors can only interact with one specific regulatory element and regualate one gene

A

false, they can spread throughout the genome and interact with multiple different genes as long as they have the same recognition sequence

59
Q

true or false, trasncription factors only interact with one promoter or gene

A

false, they will coordinately regulate multiple genes and promoters

60
Q

eukaryotic DNA response elements can be found upstream or downstream from a gene and will influence the gene expression of more than one gene which is similar to bacterial operons but they do so by regulating more than one promoter rather than a single promoter in operons

61
Q

what is epigenetic modification/ ATP-dependent chromatin remodeling

A

they are dynamic changes to chromatin structure that change their gene expression

62
Q

what is the closed conformation? open?

A

closed is when the chromatin are highly condensed and inactive in transcription. The open is when the chromatin are looser and can be actively transcribed

63
Q

why using ATP, how can chromatin be altered?

A

the structure of nucleosomes cana be changed to make DNA more accesible

64
Q

what are the four forms of ATP-dependent chromatin remodeling

A
  1. Change in relative positions of a few nucleosomes
    2> change in overall spacing
    3.) eviction or histone removal
    4) replacement of a histone variant
65
Q

is translational regulation found in eukaryotes