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Post transcriptional modifications of
transfer RNA
1
 Are adapter molecules that faithfully
translate the information in mRNA into a
specific sequence of amino acid.
 Most cells have 40-50 distinct tRNA.
 Eukaryotic cells have multiple copies of many
of the tRNA.
 Recognizes codon on mRNA
 Transcribed by RNA polymerase III
2
 Relatively small
 Consists of a single stranded of RNA folded
into a precise 3-D structure
 tRNA of bacteria & eukaryotic cytosol have
~73-93 nucleotide residues & molecular
weight of 24000-31000
3
 First nucleic acid to be completely sequenced
 Made by Robert Holley in 1965
 It contains 76 ncleotides
4
 Clover leaf structure with 5 arms
Acceptor arm
T¥C arm
D arm
Anticodon loop
Variable loop
 Trinucleotide sequence 5’- CCA-3’ at the 3’ end
5
6
Amino acid accceptor arm
It is the site of attachment of amino acid
5’-CCA-3’ sequence at the 3’ end
T¥C arm
contain a unusual base pseudouridine within the
sequencne
5’-T¥UCG-3’
Anticodon loop
contain anticodon
3 nucleotide long decoding element
D loop
contain dihydrouridines
Varible loop
size varies from 3-21 bases
 L-shaped 3-D structure
Interactions stabilising L shaped structure
1,hydrogen bond between bases
2,interactions between the bases & the sugar phosphate backbone
3,additional base stacking gained from formation of the two
extended regions of the base pairing
7
8
STEPS INVOLVED :
1,Removal of leader & tail sequence
2,Replacement of nucleotide
3,Modification of certain bases
4,Excision of intron
9
10
11
12
 Excision/splicing involves 2 steps
1,involves phosphodiester bond cleavage
catalysed by endonuclease
2,ligation reaction by RNA ligase
13
 In bacteria,introns in pre t RNA are self spliced as group I or
group II autocatalytic introns
 In archaea & eukaryotes,pre t- RNA splicing involves the
action of 3 enzymes
1, endonuclease
that recognizes & cleaves the prescursors at both end
2, ligase
that joins the the t-RNA
3, 2’phosphotransferase
that removes the 2’phosphate group on spliced t-RNA
14
 Is a heterodimeric protein
 Two catalytic subunit
Sen 34
Sen 2
 Two structural subunit
Sen 54
Sen 15
 Sen 34, sen 2 cleave 3’ & 5’splice sites
 Sen 54 determine the site of cleavage
15
16
 Homodimers or homotetramers
 Each subunit has an active site
 Recognize a structural feature called
bulge-helix-bulge
17
 The products of cleavage are a linear intron &
two half t-RNA molecules
 5’ terminus ends in a hydroxyl group
 3’ terminus ends in a 2’,3’ cyclic phosphate
group
18
 Two halves base pairs to form a t-RNA
 Using ATP further reaction occurs
Catalysed by a single enzyme with multiple
enzymatic activity
1,cyclic phosphodiesterase activity
2,kinase activity
3,ligase activity
19
20
21
22
23
24
THANK YOU

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P0st transcrotnl modfn of t rna

  • 2.  Are adapter molecules that faithfully translate the information in mRNA into a specific sequence of amino acid.  Most cells have 40-50 distinct tRNA.  Eukaryotic cells have multiple copies of many of the tRNA.  Recognizes codon on mRNA  Transcribed by RNA polymerase III 2
  • 3.  Relatively small  Consists of a single stranded of RNA folded into a precise 3-D structure  tRNA of bacteria & eukaryotic cytosol have ~73-93 nucleotide residues & molecular weight of 24000-31000 3
  • 4.  First nucleic acid to be completely sequenced  Made by Robert Holley in 1965  It contains 76 ncleotides 4
  • 5.  Clover leaf structure with 5 arms Acceptor arm T¥C arm D arm Anticodon loop Variable loop  Trinucleotide sequence 5’- CCA-3’ at the 3’ end 5
  • 6. 6 Amino acid accceptor arm It is the site of attachment of amino acid 5’-CCA-3’ sequence at the 3’ end T¥C arm contain a unusual base pseudouridine within the sequencne 5’-T¥UCG-3’ Anticodon loop contain anticodon 3 nucleotide long decoding element D loop contain dihydrouridines Varible loop size varies from 3-21 bases
  • 7.  L-shaped 3-D structure Interactions stabilising L shaped structure 1,hydrogen bond between bases 2,interactions between the bases & the sugar phosphate backbone 3,additional base stacking gained from formation of the two extended regions of the base pairing 7
  • 8. 8
  • 9. STEPS INVOLVED : 1,Removal of leader & tail sequence 2,Replacement of nucleotide 3,Modification of certain bases 4,Excision of intron 9
  • 10. 10
  • 11. 11
  • 12. 12
  • 13.  Excision/splicing involves 2 steps 1,involves phosphodiester bond cleavage catalysed by endonuclease 2,ligation reaction by RNA ligase 13
  • 14.  In bacteria,introns in pre t RNA are self spliced as group I or group II autocatalytic introns  In archaea & eukaryotes,pre t- RNA splicing involves the action of 3 enzymes 1, endonuclease that recognizes & cleaves the prescursors at both end 2, ligase that joins the the t-RNA 3, 2’phosphotransferase that removes the 2’phosphate group on spliced t-RNA 14
  • 15.  Is a heterodimeric protein  Two catalytic subunit Sen 34 Sen 2  Two structural subunit Sen 54 Sen 15  Sen 34, sen 2 cleave 3’ & 5’splice sites  Sen 54 determine the site of cleavage 15
  • 16. 16
  • 17.  Homodimers or homotetramers  Each subunit has an active site  Recognize a structural feature called bulge-helix-bulge 17
  • 18.  The products of cleavage are a linear intron & two half t-RNA molecules  5’ terminus ends in a hydroxyl group  3’ terminus ends in a 2’,3’ cyclic phosphate group 18
  • 19.  Two halves base pairs to form a t-RNA  Using ATP further reaction occurs Catalysed by a single enzyme with multiple enzymatic activity 1,cyclic phosphodiesterase activity 2,kinase activity 3,ligase activity 19
  • 20. 20
  • 21. 21
  • 22. 22
  • 23. 23