Unit 3A Transcription DNA -> RNA Flashcards

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1
Q

What is central dogma

A

dna to rna (genotype) to protein (effect or activity of protein) (phenotype)

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2
Q

nucleotide structure

A

ribose (OH - RNA vs H - DNA)
C 3 is the phosphate linkage
C5 is going to have the phospherdiester bond

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3
Q

which direction can nucleic acids grown in
which strand are we not using

A

5’ - 3’ direction
non template strand

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4
Q

Why is non template strand called coding strand

A

generate rna through transcribing the template compare to coding strand, they will be identical except Uracil will be swaped in with Thymine

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5
Q

What is RNA polymerase (RNApol)

A

transcription mediator
unravels DNA
reading strand 3 - 5 direction but building DNA on to 3’ end
many rna polymerases will be transcribing gene at same time
not all RNA’s code for proteins
large, globular enzyme with several channels running through it
active site is at intersection of channels
Holoensyme made up of core enzye which has ability to synthesize RNA and regulatory subunit (sigma factor)

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6
Q

RNApol details

A

holoenzyme - core enzyme and sigma foactor (subunit)
core enzyme polymerizing to create enzyme based on the template
sigma recognizes where the gene starts (recognizes of promoter that has to be upstream of the start of the gene)
core RNApol + sigma factor —> RNA polymerase holoenzyme

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7
Q

sigma factor

A

working upstream (-10 is ten bases up from gene)
using 2 characteristic sequences (-10 and -35 boxes) helps to start coding at right spot
they are on coding (non template strand)

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8
Q

how to stop reading transcription
aka finish transcription

A

somewhere in sequence hit a sequence that causes complementary bases to come out that cause hairpin sturcture to form
forms spontaneously
destabilizes complex and falls apart

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9
Q

how many RNA polymerates do eukaryotes have

A

3
RNApol I, II, III
RNApol II focus on

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10
Q

General Transcriction Factors

A

TATA box recognized by TBP (tata binding protein subunit of trans factor II D) leads to alignment
TFIIH pries apart double helix at transcription start point

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11
Q

What happens to mRNA before it leaves the nucleus

A

a lot of processing happens before it goes out of nucleus for translation

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12
Q

Phosphorelated tails

A

a lot of modifications associates with PT
capping factors, splicing factors, polyadenylation factors
changes can happen as transcription is going on

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13
Q

mRNA Capping

A

involves 7-methulguanosine
coding part,
poly-A tail protects from degradation extends half life

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14
Q

what is splicing

A

seperating coding stretches of the transcript from the non coding sequences
separeting exons from introns

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15
Q

coding regions are
noncoding regions are

A

exons (express, directing sequence)
introns (pulling out introns)

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16
Q

what does pre-mRNA contain

A

entire gene (introns +extrons)

17
Q

what do introns contain

A

after capping, while still being transcribed, RNA splicing (removal of introns) begins. Each intron contains few short sequences at/near its ends that are cue for its removal

18
Q

how does intron removal work

A

intron has signals at both sides
molecular machenery cut backbone, form circle
exons bond together
end up with circular intron that degrades

19
Q

what molecular machinery allows removal of introns

A

spliceosomes
has 5 small nuclear ribonucleaic particles (snRNPs)
RNA + 100 + proteins
catalutic activity provided by RNA component

20
Q

what are advantages of RNA splicing

A

can create different proteins from same gene/same primary RNA
exon skipping

21
Q

disadvantages of RNA splicing

A

more steps - more work
higher probability for mistake
makes transcription more complicated

22
Q

What needs to happen for mRNA to leave nucleus

A

5’ cap and poly-A tail are marked by protiens
exon junction complex (group of proteins) binds to properly spliced mRNAs