EXAM 2- Chapter 13/14 Flashcards

1
Q

RNA synthesis

A

all RNAs are synthesized in the nucleus
mRNA is exported to the cytoplasm and is translated
NTPs (riboNucleic TriPhosphates) are the building blocks of RNA

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2
Q

DNA replication

A

high fidelity
once and only once per cell cycle
complete
requires RNA primer to start

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3
Q

RNA Transcription

A

somewhat faithful (proofreading present but some errors occur)
not complete (only a set of genes transcribed at once)
occurs predominantly during G1/G2 phases
no primer required to start

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4
Q

RNA structure

A

ribose sugar
thymine replaced by uracil
typically single-stranded primary structure
can form double stranded secondary structure
many classes of RNA in eukaryotes

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5
Q

gene

A

any DNA sequence that is transcribed into RNA molecule

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6
Q

RNA synthesis(2)

A

RNA Polymerase leads RNA production
RNA is complimentary and antiparallel to parent strand
non-template strand= coding strand
nucleotides are added to 3’ end of RNA molecule

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7
Q

RNA synthesis steps

A

initiation of synthesis doesn’t require a primer
new nucleotides added to 3’ end of RNA molecule
DNA unwinds at the front of transcription bubble
then it re-winds

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8
Q

promoter

A

highly conserved initial binding site of RNA polymerase
specifies which polymerase is used for the different classes of genes to be transcribed
upstream of RNA coding region

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9
Q

3 major components of transcription

A

DNA template
raw materials to build new RNA molecule (NTPs)
transcription apparatus- contains proteins needed to catalyze RNA synthesis

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10
Q

Basal transcription apparatus

A

contains general transcription factors and RNA polymerase
assembles near start site
sufficient to initiate minimal levels of transcription

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11
Q

Pol2 promoter

A

consists of core and regulatory sequences

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12
Q

core promoter

A

bound by basal transcription apparatus
immediately upstream of gene
one or more consensus sequence
contains TATA box, upstream of Start site

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13
Q

regulatory promoter

A

immediately upstream of core promoter
variety of consensus sequences in different combinations
bound by transcription activator proteins- affect rate of transcription

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14
Q

consensus sequence

A

comprised of the most commonly encountered nucleotides at each site
- pyrimidines indicated by Y
- purines indicated by R
- no base in common indicated by N
- / means two bases are equally common

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15
Q

3 phases of transcription

A

initiation
elongation
termination

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16
Q

Initiation

A

Transcription factors bind to TATA box and partially unwinds DNA
more transcription factors bind
Pol2 positioned over start site
transcription bubble formed
pol2 starts transcribing

17
Q

Elongation

A

trancription factor left behind on promoter
Pol2 moves along DNA template

18
Q

Termination

A

terminal sequence
Rat 1 (5’-3’ exonuclease) digest and recycles extra pieces that arent used

19
Q

Structure of mRNA

A

5’ methyl cap (post-translational mod)
5’ untranslated region
start codon
protein-coding region
stop codon
3’ untranslated region
poly A tail (post-translational mod)

20
Q

protein-coding region

A

series of nucleotides specifying the amino acids to be added

21
Q

5’ UTR

A

necessary for ribosome binding and intron splicing

22
Q

3’ UTR

A

regulatory role in mRNA stability and translation

23
Q

Steps of pre-mRNA processing

A
  1. addition of 5’ methyl cap
  2. polyadenylation (addition of poly A tail)
  3. intron splicing
24
Q

addition of 5’ methyl cap

A

required to initiate translation
increases stability of mRNA
influences intron splicing
added during transcription

25
Q

polyadenylation

A

not coded in DNA (post-transcriptional mod.)
increase stability of mRNA
plays role in RNA export from nucleus
facilitates attachment of ribosome to mRNA
preceded by cleavage of 3’ downstream sequences

26
Q

Itron splicing

A

goal: stitch together all the exons of a gene and eliminate intron sequences
takes place in nucleus
carried out by large and complex molecular machinery (spliceosome)
consensus sequences necessary for correct splicing

27
Q

splicing introns in mRNA

A

cut and reform phosphodiester bonds
non-coding bases

28
Q

Alternative splicing

A

same gene produces identical pre-mRNA but are alternatively processed
important source of protein diversity in vertebrates
many human diseases arise from mutations that affect splicing