Lecture 8 Flashcards

1
Q

Housekeeping gene

A

Found in ALL cells (NOT specialized)

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2
Q

Multiple regulation mechanisms at

A

EACH of steps

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3
Q

Some cells make messages that by default will

A

NOT be translated

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4
Q

mRNAs contain sequences that control their translation

A

A bacterial gene’s expression can be controlled by regulating translation of its mRNA

  • Stem loop: Secondary structure formed in prokaryotes; if this is the state of the cell, the protein will be made
  • Repressor may bind and block the ribosome binding site = NO protein
  • Bacterial genes have sequences within mRNA that regulate translation
  • When temp is increased, the stem loop will dissolve or come apart and will expose the binding site and start codon, then it can be translated
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5
Q

Thermosensor

A

Found in many pathogenic bacteria; temp increases, stem loop dissolves = oxposed binding site

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6
Q

Regulatory RNAs control the expression of thousands of genes

A

MicroRNAs direct the destruction of target mRNAs

Small interfereing RNAs protect cells from infections

sRNAs (small RNAs) are used to regulate gene expression

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7
Q

An miRNA targets a complementary mRNA molecule for destruction

A

MANY genes for these; ~1/3 of protein-encoding genes are regulated by miRNA

Loop structures cut off and exported to cytoplasm -> RISC enters -> search cell for complement mRNA that isn’t needed to be translated anymore, some will have a perfect match to some message = message degraded

Micro RNAs: many complementary bases, folds back to form secondary structure (recognize as miRNA)

1) Stem loop structures cut off
2) Transported to cytoplasm; in the cytoplasm, it associates wtih the RISC (RNA induced silencing complex)
3) Get only one miRNA strand and RISC protein - search for complement to miRNA (the complement iwll be an mRNA)
4) mRNA will no longer get translated
- Could have perfect match or partial match; message is degraded regardless

miRNAs are encoded in YOUR genome; it is a way that you regulate your OWN messages

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8
Q

siRNAs are produced from double-stranded, foreign RNAs during the process of RNA interference

A

Small interfering RNA: siRNA

You do NOT encode for these, this is from a foreign source

1) Infected with double-stranded RNA -> cut up by dicer
2) Double stranded pieces of RNA associate with RISC
3) Singel stranded siRNA and RISC search for complementary message from a VIRUS
4) Degrade mRNA complement (this one can also be perfect or partial match)

RISC comes from you

siRNA cleaved by dicer -> RISC associates to siRNA -> single-stranded RNA -> search for complementary message (from virus, NOT you) -> degrade cell OR -> viral proteins produced and make you sick

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9
Q

miRNA is in OUR genome

siRNA is a FOREIGN piece

A

miRNA targets YOUR messages (preventing translation)

siRNA targets FOREIGN messages

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10
Q

RNAi can also trigger transcriptional silencing

A

RNAi = RNA interference

Can occur during process of transcription; mRNA doesn’t have to be completely processed and out in the cytoplasm for it to work

This RECRUITS proteins that will result in proteins being shut off

Transcription silencer

sRNAs associate, can occur during process of transcription, too; can recruit proteins that will turn transcription off

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11
Q

Thousands of long noncoding RNAs may also regulate mammalian gene activity

A

Long, noncoding RNAs are generally a couple hundred bases

Can also regulate gene activity: act as a scaffold or docking site

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12
Q

Long noncoding RNAs can serve as scaffolds, bringing together proteins that function in the same cell process

A

Long noncoding RNA: Act as docking site for other proteins (transcriptional activators or repressors); there to recruit anything necessary to turn transcription on or off; we regulate our genes using these as well

There is NEVER a role for double-stranded RNA in the cell; usually there because it’s a virus

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