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Comparative genomics of RNA regulatory elements

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Title: Comparative genomics of RNA regulatory elements


1
Comparative genomics of RNA regulatory elements
  • Mikhail Gelfand
  • Research and Training Center Bioinformatics
  • Institute for Information Transmission Problems
    Moscow, Russia

September 2006
2
Riboflavin biosynthesis pathway
3
5 UTR regions of riboflavin genes from various
bacteria
4
Conserved secondary structure of the RFN-element
Capitals invariant (absolutely conserved)
positions. Lower case letters strongly
conserved positions. Dashes and stars
obligatory and facultative base pairs Degenerate
positions R A or G Y C or U
K G or U B not A V not U.
N any nucleotide. X any
nucleotide or deletion
5
Attenuation of transcription
Antiterminator
Terminator
The RFN element
Antiterminator
6
Attenuation of translation
Antisequestor
SD-sequestor
The RFN element
7
RFN the mechanism of regulation
  • Transcription attenuation
  • Translation attenuation

8
Distribution of RFN-elements
Genomes Number of analyzed genomes Number of genomes with RFN Number of the RFN elements
a-proteobacteria 8 4 4
ß-proteobacteria 7 4 4
?-proteobacteria 17 15 15
d- and e-proteobacteria 3 0 0
Bacillus/Clostridium 12 12 19
Actinomycetes 9 4 4
Cyanobacteria 5 0 0
Other eubacteria 7 5 6
Total 68 47 52
9
YpaA riboflavin transporter in Gram-positive
bacteria
  • 5 predicted transmembrane segments gt a
    transporter
  • Upstream RFN element (likely co-regulation with
    riboflavin genes) gt transport of riboflaving or
    a precursor
  • S. pyogenes, E. faecalis, Listeria sp. ypaA, no
    riboflavin pathway gt transport of riboflavin
  • Prediction YpaA is riboflavin transporter
    (Gelfand et al., 1999)
  • Verification
  • YpaA transports flavines (riboflavin, FMN, FAD)
    (by genetic analysis Kreneva et al., 2000
    directly Burgess et al., 2006)
  • ypaA is regulated by riboflavin (by microarray
    expression analysis, Lee et al., 2001)
  • via attenuation of transcription (and to some
    extent inhibition of translaition) (Winkler et
    al., 2003)

10
Phylogenetic tree of RFN-elements
11
thi-box and regulation of thiamine metabolism
genes by thiamine pyrophosphate (Miranda-Rios et
al., 2001)
12
Alignment of THI-elements
13
Conserved secondary structure of the THI-element
Capitals strongly conserved positions. Dashes
and points obligatory and facultative base pairs
Degenerate positions R A or G Y C or U K
G or U M A or C N any nucleotide
14
THI the mechanism of regulation
  • Transcription attenuation
  • Bacillus/Clostridium group,
  • Thermotoga,
  • Fusobacterium,
  • Chloroflexus
  • Thermus/Deinococcus group,
  • CFB group
  • Proteobacteria,
  • Translation attenuation
  • Actinobacteria,
  • Cyanobacteria,
  • Archaea

15
Distribution of THI-elements
Genomes Number of analyzed genomes Number of genomes with THI Number of the THI elements
a-proteobacteria 7 7 15
b-proteobacteria 6 6 12
g-proteobacteria 18 17 38
e- and d-proteobacteria 3 1 1
The Bacillus/Clostridium group 18 18 51
Actinomycetes 9 9 25
Cyanobacteria 5 5 5
Other eubacteria 14 11 11
Archaea (Thermoplasma) 17 3 6
Total 97 77 164
Mandal et al., 2003 THI in 3UTR (plants). THI
in untranslated intron (fungi)
16
Metabolic reconstruction of the thiamin
biosynthesis
thiN
Transport of HET
Transport of HMP
(Gram-positive bacteria)
(Gram-negative bacteria)
17
Metabolic reconstruction of the thiamin
biosynthesis
thiN
Transport of HET
Transport of HMP
(Gram-positive bacteria)
confirmed (Morett et al., 2003 )
(Gram-negative bacteria)
18
The PnuC family of transporters
THI elements
RFN elements
19
B12-box and regulation of cobalamin metabolism
genes by cobalamine (Nou Kadner, 2000 Ravnum
Andersson, 2001 Nahvi et al., 2002)
  • Long mRNA leader is essential for the regulation
    of btuB by vitamin B12.
  • Involvement of a highly conserved B12-box
    rAGYCMGgAgaCCkGCcd in the regulation of the
    cobalamin biosynthetic genes (E. coli, S.
    typhimurium)
  • Post-transcriptional regulation RBS-sequestering
    hairpin is essential for the regulation of the
    btuB and cbiA
  • Ado-CBL is an effector molecule involved in the
    regulation of the cobalamin biosynthesis genes

20
Conserved RNA secondary structure of the
regulatory B12-element
21
The predicted mechanism of the B12-mediated
regulation of cobalamin genes formation of a
pseudoknot
22
Distribution of B12-elements in bacterial genomes
B12-element regulates cobalamin biosynthetic
genes and transporters, cobalt transporters and a
number of other cobalamin-related genes.
23
Metabolic reconstruction of cobalamin
biosynthesis new enzymes and transporters
24
Metabolic reconstruction of cobalamin
biosynthesis new enzymes and transporters
confirmed (Woodson et al., 2004)
recently confirmed (Zayas et al., 2006)
25
If a bacterial genome contains B12-dependent and
B12-independent isoenzymes, the genes encoding
the B12-independent isoenzymes are regulated by
B12-elements
Ribonucleotide reductases Ribonucleotide reductases
NrdJ (B12-dependent) NrdAB/NrdDG (B12-independent)



Methionine synthase Methionine synthase
MetH (B12-dependent) MetE (B12-independent)



26
If a bacterial genome contains B12-dependent and
B12-independent isoenzymes, the genes encoding
the B12-independent isoenzymes are regulated by
B12-elementsnrdAB in Streptomyces coelicolor
experimental confirmation in (Borovok et al.,
2005)
Ribonucleotide reductases Ribonucleotide reductases
NrdJ (B12-dependent) NrdAB/NrdDG (B12-independent)



Methionine synthase Methionine synthase
MetH (B12-dependent) MetE (B12-independent)



27
LYS-element, a.k.a. L-box lysine riboswitch
28
Reconstruction of the lysine metabolism
predicted genes are boxed (pathway of acetylated
intermediates in B. subtilis)
29
Regulation of the lysine catabolism the first
example of an activating riboswitch
  • LYS-elements upstream of the pspFkamADEatoDA
    operon in Thermoanaerobacter tengcongensis
    kamADElysE operon in Fusobacterium nucleatum
  • lysine catabolism pathway
  • LYS element overlaps candidate terminator
  • gt acts as activator
  • similar architecture of activating adenine
    riboswitch upstream of purine efflux pump ydhL
    (pbuE) in B. subtilis (Mandal and Breaker, 2004)

30
S-box (SAM riboswitch)
Grundy and Henkin, 1998
31
Reconstruction of the methionine metabolism
predicted genes are boxed and marked by
(transport, salvage cycle)
32
A new family of amino acid transporters
S-box (rectangle frame)MetJ (circle
frame)LYS-element (circles)Tyr-T-box
(rectangles)
malate/lactate
33
Repression of reverse pathway Met ? Cysin
Clostridium acetobutylicum in the presence of
Cys and absence of Met
34
Firmicutes
Loss of S-boxes
Lactobacillales Met-T-box (Met-tRNA-dependent
attenuator)
Streptotoccales MtaR (transcription
factor) SAM-III riboswitch (metK) (the Henkin
group)
Bacillales S-box
Clostridiales S-box
proteobacteria
  • Other genomes with S-boxes the Zoo
  • Petrotoga
  • actinobacteria (Streptomyces, Thermobifida)
  • Chlorobium, Chloroflexus, Cytophaga
  • Fusobacterium
  • Deinococcus

E.coliTFs
Xanthomonas S-box
alphas SAM-II
Geobacter S-box
Need more genomes
35
Riboswitches in metagenomes
new functions S-box eukaryotic-type translation
initiation factor eIF-2B (COG0182) B12-box
fatty-acid desaturase (COG1398) GCVT malate
synthase glcB, phosphoserine aminotransferase serC
36
Riboswitch composition of metagenomes
total per 100 000
contigs 47 27 26
37
Riboswitches in metagenomes by taxonomy
62
44
30
26
19
15
11
8
total per 100 000 contigs
3
38
Conserved structures of riboswitches (circled
X-ray)
39
Mechanisms
gcvT ribozyme, cleaves its mRNA (the Breaker
group)THI-box in plants inhibition of splicing
(the Breaker and Hanamoto groups)
40
Characterized riboswitches (more are predicted)
RFN Riboflavin biosynthesis and transport FMN (flavin mononucleotide) Bacillus/Clostridium group, proteobacteria, actinobacteria, other bacteria
THI Biosynthesis and transport of thiamin and related compounds TPP (thiamin pyrophosphate) Bacillus/Clostridium group, proteobacteria, actinobacteria, cyanobacteria, other bacteria, archea (thermoplasmas), plants, fungi
B12 Biosynthesis of cobalamine, transport of cobalt, cobalamin-dependent enzymes Coenzyme B12 (adenosyl-cobalamin) Bacillus/Clostridium group, proteobacteria, actinobacteria, cyanobacteria, spirochaetes, other bacteria
S-boxSAM-IISAM-III Metabolism of methionine and cystein SAM (S-adenosyl- methionine) Bacillus/Clostridium group and some other bacteriaSAM-II (alpha), SAM-III (Streptococci)
LYS Lysine metabolism lysine Bacillus/Clostridium group, enterobacteria, other bacteria
G-box Metabolism of purines purines Bacillus/Clostridium group and some other bacteria
glmS (ribozyme) Synthesis of glucosamine-6-phosphate glucosamine-6-phosphate Bacillus/Clostridium group
gcvT (tandem) Catabolism of glycine glycine Bacillus/Clostridium group
41
Properties of riboswitches
  • Direct binding of ligands
  • High conservation
  • Including unpaired regions tertiary
    interactions, ligand binding
  • Same structure different mechanisms
    transcription, translation, splicing, (RNA
    cleavage)
  • Distribution in all taxonomic groups
  • diverse bacteria
  • archaea thermoplasmas
  • eukaryotes plants and fungi
  • Correlation of the mechanism and taxonomy
  • attenuation of transcription (anti-anti-terminator
    ) Bacillus/Clostridium group
  • attenuation of translation (anti-anti-sequestor
    of translation initiation) proteobacteria
  • attenuation of translation (direct sequestor of
    translation initiation) actinobacteria
  • Evolution horizontal transfer, duplications,
    lineage-specific loss
  • Sometimes very narrow distribution evolution
    from scratch?

42
Study scenarios
  • RFN, S-box
  • early identification of a conserved element
  • model of regulation from comparative analysis
  • use for functional annotation
  • experimental validation
  • THI, B12, PUR, LYS
  • scavenging of unexplained published experimental
    results
  • models of regulation from comparative analysis
  • experimental validation
  • use for functional annotation
  • GcvT, GlmS
  • large-scale computational screens
  • prediction of ligand from functions of regulated
    genes
  • experimental validation
  • SAM-II, SAM-III
  • gaps in regulatory systems
  • computational screens
  • experimental validation
  • Structures PUR, THI, S-box

43
Teaser Systematic analysis of T-boxes
  • T-boxes the mechanism (Grundy Henkin)

44
Partial alignment of predicted T-boxes
TGG T-box
Aminoacyl-tRNA synthetases
Amino acid biosynthetic genes
Amino acid transporters
45
continued (in the 5 direction)
anti-anti (specifier) codon
Aminoacyl-tRNA synthetases
Amino acid biosynthetic genes
Amino acid transporters
46
800 T-boxes in 90 bacteria
  • Firmicutes
  • aa-tRNA synthetases
  • enzymes
  • transporters
  • all amino acids excluding glutamine, glutamate,
    lysine
  • Actinobacteria (regulation of translation
    predicted)
  • branched chain (ileS)
  • aromatic (Atopobium minutum)
  • Delta-proteobacteria
  • branched chain (leu enzymes)
  • Thermus/Deinococcus group (aa-tRNA synthases)
  • branched chain (ileS, valS)
  • glycine
  • Chloroflexi, Dictyoglomi
  • aromatic (trp enzymes)
  • branched chain (ileS)
  • threonine

47
Same enzymes different regulators (common part
of the aromatic amino acids biosynthesis pathway)
cf. E.coli AroF,G,H feedback inhibition by TRP,
TYR, PHE transcriptional regulation by TrpR, TyrR
48
Recent duplications and bursts ARG-T-box in
Clostridium difficile
49
(No Transcript)
50
More duplications THR-T-box in C. difficile
51
ASN/ASP/HIS T-boxes Duplications and changes in
specificity
52
Blow-up
53
Branched-chain amino acids duplications and
changes in specificity
ATC
CTC
ATC
54
Blow-up
transporter
ATC
GTC
dual regulation of common enzymes
ATC
CTC
55
Double and one-and-a-half T-boxes
  • TRP trp operon (Bacillales, C. beijerincki, D.
    hafniense)
  • TYR pah (B. cereus)
  • THR thrZ (Bacillales) hom (C. difficile)
  • ILE ilv operon (B. cereus)
  • LEU leuA (C. thermocellum)
  • ILE-LEU ilvDBNCB-leuACDBA (Desulfotomaculum
    reducens)
  • TRP trp operon (T. tengcongensis)
  • PHE arpLA-pheA (D. reducens, S. wolfei)
  • PHE trpXY2 (D. reducens)
  • PHE yngI (D. reducens)
  • TYR yheL (B. cereus)
  • SER serCA (D. hafniense)
  • THR thrZ (S. uberis)
  • THR brnQ-braB1 (C. thermocellum)
  • HIS hisXYZ (Lactobacillales)
  • ARG yqiXYZ (C. difficile)

56
  • Andrei Mironov
  • software genome analysis, conserved RNA patterns
  • Alexei Vitreschak
  • analysis of RNA structures
  • Dmitry Rodionov
  • metabolic reconstruction
  • Support
  • Howard Hughes Medical Institute
  • INTAS
  • Russian Fund of Basic Research
  • Russian Academy of Sciences
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