1-9 Transcription & RNA processing Flashcards

1
Q

DNA coding strand

A

matches the mRNA

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2
Q

DNA template strand

A

the strand polymerase actually reads in order to transcribe a mRNA for the desired coding strand

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3
Q

Pol 1

A

rRNA

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4
Q

Pol 2

A

protein encoding, most snRNA

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5
Q

Pol 3

A

small RNA subunits

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6
Q

Non-template dependent polymerase

A

polyadenylate pol -> polyA of mRNA

PARP -> protein modification

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7
Q

POLRMT

A

polymerase for mitochondrial RNA

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8
Q

Distribution of elements over chromosomes

A
  • satellite dna near centromere
  • ribosomal genes near telomeres
  • tandem repeats: same genes near each other replicated
  • interspersed retrotransposons: SINES, LINES

some chromosomes gene rich some gene poor

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9
Q

Transcription/processing of rRNA

A
  1. internally transcribed spacers within transcript
  2. chemical modifications: used for folding help
  3. ITS removed and diff subunits formed

Happens in nucleolus, requires small rnas to help cleave and form, exports small and large subunits into cytosol and they only come together when initiation of translation has started

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10
Q

Processing/maturation of tRNA

A
transcribed in nucleus
removes introns
forms stem loops
modifes bases and CCA sequence added to 3' tail
exported
AA attached to A of CCA tail
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11
Q

Components of RNA pol II transcribed genes

A

proximal control elements: GC box , CAAT box
core promoter: TATA box
+1 (first base of translation)
Exons/introns

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12
Q

Initiation of pol II transcription

A

Basal transcription factors associate with start site/TATA box, other factors recruited and RNA pol II now joins, pol II get phosphorylated on “tail” signaling transcription to occur

tail contains: capping factors, splicing factors, polyA factors to all process the mRNA immediately

enhancers/regulators effect this process

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13
Q

Enhancers

A

activity of promoter increase/decreased by

specific DNA sequence to which REGULATORY PROTEINS can bind

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14
Q

Mech of pre-mRNA splicing

A
  1. SnRNPs bind sequences for splice donor/acceptor and recuit complex
  2. middle branch site initiates nuclophilic attach on splice donor, makes lariat loop
  3. acceptor site cleaved and ligated to donor end
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15
Q

Cryptic splice site

Alternate slice sites

A

make new/mutant proteins, pathological, can truncate of lengthen 3UTR based on differ splice sites and addition of AAA tail location

healthy normal, method of making protein isoforms

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16
Q

Nuclear export of processed mRNAs

A

Once mRNA fully transcribed, “exon junction complex” and “cap binding protein” still associated with transcript to allow export through nuclear pore complex

Exon jucntion complex stays bound in cytosol as a proofreaded to show to translation machinery that made correctly

cap binding protein exchanged for cytosol cap