Chapter 17 - Gene Expression Flashcards

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1
Q

is RNA usually double or single stranded

A

single

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2
Q

what is transcription?

A

the synthesis of RNA using information from DNA

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3
Q

what is mRNA?

A

for a protein coding gene, the resulting complementary RNA strand is a transcript of the gene’s protein building instructions and is called mRNA because it carries a genetic message form DNA to ribosomes

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4
Q

what is translation?

A

the synthesis of a polypeptide using information in the mRNA

RNA is translated into amino acid sequence of a polypeptide

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5
Q

what is coupling? where does it occur?

A

bacteria don’t have nuclei so their DNA isn’t separated by nuclear membranes from ribosomes –> coupling means that ribosomes can attach to the 5’ end of a mRNA molecule while it is being made by transcription from the DNA template

in eukaryotic cell, the nuclear envelope separates transcription and translation

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6
Q

what is RNA?

A

a sequence of ribonucleotides complementary to a DNA template

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7
Q

What are the stop codons?

A

UAA, UGA, UAG

Don’t encode amino acids

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8
Q

What’s the start codon for translation

A

AUG

Also codes for Met

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9
Q

Difference between RNA and DNA polymerase?

A

RNA polymerase doesn’t need a primer!

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10
Q

What’s a promoter?

A

A DNA sequence where RNA polymerase attaches and initiates transcription

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11
Q

What does RNA pol I do?

A

Synthesize rRNA

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12
Q

What does RNA pol II do?

A

Synthesizes mRNA

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13
Q

What does RNA pol III do?

A

Synthesizes tRNA

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14
Q

Set up of transcription

A

Promoter contains within it the start point –> RNA pol II binds to promoter only after transcription factors are attached to the promoter

The entire complex of transcription factors and RNA pol II bound to the promoter is called the transcription initiation complex

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15
Q

What unwinds the DNA and starts transcription?

A

RNA pol II

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16
Q

What’s the TATA box?

A

A nucleotide sequence within the promoter that upstream from the start point - a transcription factor has to bind to it first before RNA pol II can bind to DNA

17
Q

Elongation during transcription

A

A single gene can be transcribed simultaneously by multiple polymerase molecules, like a convoy –> increases amount of mRNA transcribed so cell can encode protein in large amounts

18
Q

Prokaryote vs eukaryotes termination of transcription

A

Bacteria: DNA goes through transcribed terminator sequence, detaches, and requires no further modification

Eukaryotes: RNA pol II transcribed a sequence from the DNA called the polyadenylation sequence (AAUAAA) –> 10 nucleotides downstream, certain proteins cut the DNA free from the polymerase and free the pre-mRNA –> RNA pol II continues to transcribe but new 5’ end isn’t protected by a cap so it’s degraded

19
Q

What is a 5’ cap

A

A modified form of guanine that’s added after transcription of the first 20-40 nucleotides

20
Q

What is a poly A tail?

A

After polyadenylation signal is transcribed and pre-mRNA is set free, enzyme then adds 50-200 more adenine (A) nucleotides

21
Q

RNA splicing

A

RNA splicing removes large portions of RNA that are initially synthesized

The noncoding segments of nucleic acid in RNA that lie between coding regions are called introns

The other regions are called exons because they will eventually be EXpressed (translated into amino acids)

22
Q

What removes introns from pre-mRNA

A

Removal of introns is accomplished by a large complex of proteins and small RNA called a spliceosome

23
Q

What is alternative RNA splicing

A

A single gene can encode more than more kind of polypeptide depending on which segments are treated as exons during RNA processing!

24
Q

What are the two ends of a tRNA

A

The 3’ end protrudes and is the attachment site for an amino acid

The other end is the anticodon which is the nucleotide triplet that base pairs to a specific mRNA codon

25
Q

What correctly matches up tRNA with its appropriate amino acid

A

Aminoacyl-tRNA synthetases –> the active site of each synthetases fits only a specific combination of tRNA and amino acid but each synthetases can fit all the tRNA for the specific amino acid

Catalyzes covalent attachment of amino acid to tRNA in a process driven by hydrolysis of ATP

26
Q

What is wobble

A

There isn’t a tRNA for each mRNA because there is flexible base pairing –> tRNA anticodon UCU can pair with mRNA codon AGA or AGG which both for for arginine

Difference is usually in the third codon

27
Q

Where are the subunits of ribosomes made?

A

Nucleolus

28
Q

Eukaryotic vs bacterial ribosomes

A

Eukaryotic are larger and different in molecular composition which is significant because certain antibiotic drugs can inactivate bacterial ribosomes without affecting eukaryotic ribosomes

29
Q

rRNA in translation

A

It’s primarily responsible for both structure and function of the ribosome and acts as a catalyst of peptide bond formation

30
Q

What energy does translation use

A

GTP

31
Q

What are the different ends of the polypeptide chain?

A

The chain is synthesized in one direction from the initial Met at the amino end called the N-terminus towards the final amino acid at the carboxyl end called the C-terminus

Amino acids are added one by one at the C-terminus

32
Q

Free vs bound ribosomes

A

Free ribosomes are suspended in the cytosol and synthesize proteins that say in the cytosol

Bound ribosomes are attached to the ER or nuclear envelope and make proteins of the engine brand system as wrk a proteins to be secreted from the cell

Ribosomes can alternate between being free or bound

33
Q

What are missense mutations?

A

Substitutions that change one amino acid to another

Don’t always do damage because functions of the amino acids can be similar to each other

34
Q

What’s a nonsense mutation

A

A point mutation that changes the codon for an amino acid into a stop codon and causes translation to be terminated prematurely –> resulting polypeptide will be shorter than the polypeptide encoded by the normal genes which usually leads to nonfunctional proteins

35
Q

What’s a frameshift mutation?

A

Occurs whenever the number of nucleotides added or deleted aren’t multiples of three and the result is missense which usually ends in nonsense and premature termination

Insertion or deletion usually alter the reading frame so the triplet groups are messed up –> usually worse than substitutions