Unit 14- RNA Flashcards

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1
Q

gene organization

A
  • concept of colinerarity and noncolinearity
  • # of nucleotides in a gene should be proportional to the # of amino acids in encoded protein
  • DNA much longer than mRNA (hybridization)
  • bacteria = colinear; eukaryotes = noncolinear (loops)
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2
Q

colinearity

A

continuous seq of nucleotides in DNA encodes a continuous sequence of amino acids in a protein

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3
Q

introns

A
  • eukaryotes have introns and exons
    -later REMOVED by RNA processing
  • # and size vary between genes
  • common in eukaryotes; uncommon in bacteria
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4
Q

group 1 introns

A
  • Location: some rRNA genes
  • mechanism: self-splicing
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5
Q

group 2 introns

A
  • Location: protein-encoding genes in mitochondria and chloroplast
  • mechanism: self-splicing
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6
Q

nuclear-premRNA introns

A
  • Location: protein-encoding genes in the nucleus of eukaryotes
  • mechanism: spliceosomal (snRNA)
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7
Q

tRNA introns

A
  • Location: tRNA genes
  • mechanism: enzymatic
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8
Q

gene

A
  • DNA sequences that code for all exons and introns
  • Sequences at the beginning and end of the RNA are not translated into a protein
    -The promoter
    -The terminator
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9
Q

structure of RNA

A
  • mature mRNA contains 5’ untranslated region (5’ UTR, or leader seq)
  • Shine-Dalgarno seq (prokaryotes)
  • protein-coding region
  • 3’ untranslated region
    (3’ and 5’: stability and reg of translation NOT aa encoding)
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10
Q

start codon

A

AUG (met)

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11
Q

stop codons

A
  • UAA
  • UAG
  • UGA
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12
Q

pre-mRNA processing

A
  • addition of 5’ cap: nucleotide with 7-methylguanine; 5’-5’ bond to 5’ end
  • addition of poly(A) tail: 50-250 adenine nucleotides added to 3’ end
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13
Q

5’ cap

A

facilitates bingind of ribosomes to 5’ end of mRNA, increasing mRNA stability

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14
Q

3’ clevage and addition of poly(A) tail

A

inc stability of mRNA, facilitates binding of ribosomes

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15
Q

RNA splicing function

A

removes noncoding introns, facilitates mRNA export to cytoplasm, allows mult protein production from alt splicing

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16
Q

RNA editing

A

alters nuckeotide seq of mRNA

17
Q

RNA splicing

A

consensus seq
- 5’ consensus seq: GU(A/G): 5’ splice site
- 3’ consensus seq: CAGG
- branch point: adeine “A”: ~18-40 nucleotides upstream of 3’-splicing site

spliceosome: five RNA molecules +300 proteins

18
Q

steps of splicing

A
  1. 5’ end cleaves from the upstream exon and attatched to branch point to form a LARIAT
  2. 3’ end of intron is cleaved from downstream exon, and ends of the 2 exons are spliced together
  • takes place in spiceosome
19
Q

nuclear organization

A
  • intron removal, mRNA processing, and transcription take place at same site in nucleus
20
Q

minor splicing

A
  • 2-tpes of self-splicing introns: group 1 and 2 (due to complez secondary structure)
  • occur in some protist rRNA and in fungi mitochondria
21
Q

alt processing pathways for processing pre-mRNA

A
  • enables exons to be spliced together in different combinations to yield different proteins
  • due to Multiple 3’ cleavage sites
22
Q

RNA editing

A
  • guide RNA pairs with mRNA
  • template for addition, deletion, or alteration of bases
23
Q

structure of tRNA

A
  • rare modified RNA nucleotide bases (robothymine and pseudouridine)
    • produced by chem alt of standard bases
  • common secondary structure: cloverleaf
  • anticodon
24
Q

structure of ribosome

A
  • large ribosome subunit
  • small ribosome subunit
25
Q

ribosomal RNA is processed after transcription

A
  • methyl groups added
  • RNA cleaved into several pieces
  • trimmed
  • mature rRNA molecules(subunits) produced
26
Q

RNA interfering

A

limits the invasion of foreign genes and censors the expression of their own genes

27
Q

Long Noncoding RNAs

A
  • do not encode proteins
  • control gene expression
  • enhancer RNAs are transcribed from enhancers and control gene expression