1
An Improved Search Algorithm to Find G-Quadruplexes in Genome
Sequences
Anna Varizhuk
1,2
, Dmitry Ischenko
1
, Igor Smirnov
1
, Olga Tatarinova
1
, Vyacheslav Severov
1
,
Roman Novikov
2,3
, Vladimir Tsvetkov
1,4
, Vladimir Naumov
1
, Dmitry Kaluzhny
2
, Galina
Pozmogova
1*
1
Institute for Physical-Chemical Medicine, Malaya Pirogovskaya Str., 1a, Moscow 119435,
Russia;
2
Engelhardt Institute of Molecular Biology, Vavilov Str., 32 Moscow 119991, Russia;
3
N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, Moscow 119991, Russia;
5
Topchiev Institute of Petrochemical Synthesis, Leninsky Prospect, 29, Moscow 119991, Russia.
*Corresponding author
Keywords: noncanonical DNA structures, G-quadruplexes, search algorithm
this version posted January 23, 2014. ; https://doi.org/10.1101/001990doi: bioRxiv preprint
2
ABSTRACT
A growing body of data suggests that the secondary structures adopted by G-rich polynucleotides
may be more diverse than previously thought and that the definition of G-quadruplex-forming
sequences should be broadened. We studied solution structures of a series of naturally occurring
and model single-stranded DNA fragments defying the G
3+
N
L1
G
3+
N
L2
G
3+
N
L3
G
3+
formula, which
is used in most of the current GQ-search algorithms. The results confirm the GQ-forming
potential of such sequences and suggest the existence of new types of GQs. We developed an
improved (broadened) GQ-search algorithm (http://niifhm.ru/nauchnye-issledovanija/otdel-
molekuljarnoj-biologii-i-genetiki/laboratorija-iskusstvennogo-antitelogeneza/497-2/) that
accounts for the recently reported new types of GQs.
INTRODUCTION
Non-canonical polynucleotide structures play an important role in biogenesis processes, such as
transcription, DNA repair, replication, translocation and RNA splicing (Saini et al. 2013). A
clear view of DNA/RNA secondary structures and dynamics is necessary to understand the
mechanisms of genomic regulation and to identify new biomarkers of pathology and drug
targets. A growing body of data suggests that the secondary structures adopted by G-rich
polynucleotides may be more diverse than previously thought (Kaluzhny et al. 2009; Tomasko et
al. 2009; Guedin et al. 2010; Amrane et al. 2012; Beaudoin et al. 2013; Mukundan and Phan
2013). For instance, two new types of G-quadruplexes (GQs) have recently been reported: GQs
with mismatches (Tomasko et al. 2009) and GQs with bulges (Mukundan and Phan 2013)
(Figure 1). GQs with bulges (bGQs) are GQs in which two stacked tetrad-forming guanosines in
one column are separated by a projecting nucleoside. GQs with mismatches (mGQs) contain one
or more substitutions of G for other nucleotides in the tetrads. (The mismatching nucleosides
may participate in stacking). Both types of structures appeared to be stable under physiological
conditions. These findings have led the researchers to the conclusion that the definition of GQ-
forming sequences should be broadened. All currently available online search tools for GQs
(Quad finder (Scaria et al. 2006), QGRS Mapper (Kikin et al. 2006) and QGRS predictor
(Menendez et al. 2012)) employ the G
3
+N
L1
G
3
+N
L2
G
3
+N
L3
G
3
+ formula, which only defines
canonical (‘perfect’) GQs.
We present here the first GQ-search tool, imGQfinder, that accounts for noncanonical
(‘imperfect’) quadruplex structures (imGQs; i.e., bGQs and mGQs) in addition to canonical
GQs. The ImGQfinder tool is freely accessible at the URL http://niifhm.ru/nauchnye-
issledovanija/otdel-molekuljarnoj-biologii-i-genetiki/laboratorija-iskusstvennogo-
antitelogeneza/497-2/
.
Structural studies of a series of
(
G
3+
N
L1
G
3+
N
L2
G
3+
N
L3
G
3+
)-defying
oligonucleotides (ONs), whose imGQ-forming potential was predicted by imGQfinder, were
performed to verify our improved GQ-search algorithm. We also utilize ImGQfinder for
statistical analysis of the imGQ-motif distribution in the human genome.
RESULTS
ImGQ-motif definition and ImGQfinder interface (algorithm implementation)
In our broadened algorithm, we search for G-runs, determine the distance between them and
select fragments that comply with the predetermined conditions for the maximum length of GQ
loops and the minimum number of nucleotides in a G-run (i.e., the number of tetrads). The
this version posted January 23, 2014. ; https://doi.org/10.1101/001990doi: bioRxiv preprint
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imGQ motif definition for imGQs with single defects is presented in Table 1. ImGQs with
multiple defects can also be analyzed, but the relative set of formulas is not shown. Apparently,
most imGQ motifs can be interpreted as both putative bGQs and mGQs. Some imGQs may also
turn out to be ‘perfect’ GQs with fewer tetrads, e.g., a putative 3-tetrad imGQ with a bulge or a
mismatch in the external tetrad can theoretically adopt the canonical 2-tetrad GQ conformation.
ImGQfinder searches for all GQ and imGQ motifs, including overlapping ones. The program is
implemented in Perl. The graphical user interface was developed using the Tk library. The inputs
include the queried nucleotide sequence in fasta format, the number of tetrads and defects and
the maximum loop length. The hits are displayed in a table. The coordinates of each G-run start
(G1, G2, G3 and G4) and the positions of the defects (DEFECT) in each imGQ-forming
fragment are shown. The user can also see the full sequences of the putative GQs or imGQs (the
‘Add sequence to output’ option).
In addition, we offer an application that can determine overlapping GQ/imGQ sites in the form
of a single lengthy fragment with GQ/imGQ-forming potential (the ‘Add intersected output’
option). This feature is useful for estimating the maximum number of quadruplexes that can exist
simultaneously.
Structural studies (algorithm verification)
Although several recent publications contain direct evidence for the existence of imGQs that are
stable under physiological conditions, such structures are still relatively new, and there are few
examples of well-characterized imGQs. To complement the studies on imGQ structures and to
verify our search algorithm for imGQs, we synthesized a set of naturally occurring and model
single-stranded DNA fragments that were defined by ImGQfinder to be putative imGQs and
GQs, and we analyzed their conformations in solution using physicochemical methods. The ONs
are listed in Table 2.
The sequences Bcl, Ct1 and PSTP were taken from the human genome. Bcl is located in the
BCL2 promoter region 42 nucleotides upstream of the translation start site (NCBI Reference
Sequence: NC_000018.9, chr18: -60985942 to -60985966). Ct1 is located in the intron of the
CTIF gene (NCBI Reference Sequence: NC_000018.9, chr18: +46379322 to +46379344). PSTP
is located at the PSTPIP2 intron/boundary (NCBI Reference Sequence: NC_000018.9, chr18: -
43572049 to -43572072). BclG, BclA, BclT, Bcl-tr (truncated), Ct2, Ct3, Ct4, CtA, CtC and
CTG are mutants of Bcl and Ct1. G3, G3A, G4, G4A and G4AA are model sequences. The
solution structures of the ONs were investigated using UV-melting experiments, CD
spectroscopy and NMR spectroscopy. The rotational relaxation times of EtBr in complex with
the ONs are proportional to the hydrodynamic volumes of the molecules, and these times were
estimated to distinguish between monomolecular and intermolecular quadruplexes. The melting
temperatures of monomolecular GQs/imGQs and the GQ characteristics determined from the CD
data (parallel, antiparallel or mixed GQ folding) are given in Table 1. Fragments of the
1
H-NMR
spectra and CD spectra of the ONs Bcl, Ct1 and their mutants are shown in Figure 2. For the
UV-melting profiles, molecularity analysis, CD spectra of the model ONs G3, G4 and their
mutants and all the corresponding experimental procedures, see the supporting information.
The ONs G4, G3, CtG and BclG can fold into perfect 4-tetrad (G4, CtG and BclG) and 3-tetrad
(G3) GQs according to the conventional GQ definition. Indeed, all of them formed highly stable
this version posted January 23, 2014. ; https://doi.org/10.1101/001990doi: bioRxiv preprint
4
parallel (G3
1
, G4 and CTG) or mixed (BclG) GQs in the presence potassium salt, as evidenced
by the CD spectra and the UV-melting profiles. The imino region of the BclG
1
H-NMR spectrum
(Figure 2) contains 16 signals, which is consistent with 4 G-tetrads.
The ONs BclT, G4A, G4AA, Ct1-Ct4, CtA, CtC and PSTP defy the conventional
G
3+
N
L1
G
3+
N
L2
G
3+
N
L3
G
3+
formula and would be omitted by the currently existing GQ-search
algorithms. ImGQfinder defines all of these sequences to be putative imGQs. Indeed, all these
ONs form stable monomolecular quadruplexes in the presence of potassium salt. Fourteen
signals in the imino regions of the
1
H-NMR spectra of the ONs Ct1 and PSTP are consistent with
4-tetrad mGQ structures with one imperfect tetrad
2
. Twelve signals in the imino-spectrum region
of ribo-Ct1 most likely suggest a 3-tetrad bGQ structure (Molecular modeling studies were
performed to clarify the Ct1 structure. For more information, see the supporting data).
Importantly, the ONs BclT and G4aa cannot even form 2-tetrad GQs according to the
conventional GQ definition. However, these ONs appear to fold into rather stable GQ-like
structures under physiological conditions. These results confirm that ImGQfinder can be used to
predict the possibility of bGQ and mGQ formation.
ImGQs in the human genome: statistical analysis (algorithm application)
ImGQfinder was utilized to reassess the abundance and to analyze the distribution of putative
quadruplex sites in the human genome. We only considered 4-tetrad GQs and imGQs, which are
generally more stable than 2- and 3-tetrad GQs according to the literature and our own
physicochemical data. The sequences representing overlapping GQ/imGQ sites were counted
only once (this was performed using an application feature of ImGQfinder). Sites with both GQ-
and imGQ-folding potentials were regarded as putative GQs because the latter are generally
more stable. As expected, imGQs are substantially more abundant than GQs (Table 3). Thus, the
maximum overall number of quadruplex-like structures realized in vivo may be significantly
higher than previously thought. The distribution of putative imGQs and GQs within RefSeq
genes (genomic sequences used as reference standards for well-characterized genes;
http://www.ncbi.nlm.nih.gov/refseq/rsg/about/
) is shown in Figure 3 (for a more detailed
analysis, see the supporting information). As expected, imGQs are substantially more abundant
than GQs.
To additionally validate the ImGQfinder algorithm, we also calculated the number of all putative
non-overlapping ‘perfect’ 3-tetrad guadruplexes in the human genome and compared it with the
literature data. The obtained value (359 k) is close to the previous estimations (376 k) (Huppert
and Balasubramanian 2005).
DISCUSSION
A new GQ-search algorithm, which is based on a broadened definition of quadruplex-forming
sequences, and the user-friendly online tool ImGQfinder were developed. The algorithm was
verified by structural studies of a series of ONs whose imGQ-forming potential was predicted by
1
G3 demonstrated extreme stability in potassium, and the stability was even superior to that of G4. We attribute this
stability to the fact that single-nucleotide fragments separating G runs fit perfectly well in the diagonal loops of 3-
tetrad GQs but may be slightly too short for 4-tetrad diagonal loops.
2
One imperfect tetrad contains three Hoogsteen-bound Gs with two imino G protons that participate in H-bonding,
which results in two additional signals in the relative region of the
1
H-NMR spectrum.
this version posted January 23, 2014. ; https://doi.org/10.1101/001990doi: bioRxiv preprint
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imGQfinder. Importantly, the physicochemical properties of ImGQs and GQ, such as the thermal
stability under physiological conditions, appear to be rather similar.
Reassessment of the abundance of putative quadruplex sites in the human genome with
imGQfinder revealed that the maximum number of G4 structures that could be simultaneously
realized has been underestimated. As is evident from Figure 3, putative GQ and imGQ sites have
basically similar distributions within RefSeq genes. Exons tend to be depleted of both GQs and
imGQs. Large clusters of putative GQ/imGQ sites were found in the introns near the intron/exon
boundaries and in the promoters that are approximately 100 bp downstream of the transcription
start site. GQ clustering in 5’ untranslated regions is consistent with literature data (Huppert and
Balasubramanian 2007; Maizels and Gray 2013). The results of several recent studies suggest 5’-
UTR GQ participation in transcription and translational regulation (Huppert et al. 2008). GQs at
intron/exon boundaries may play a role in splicing. Although known enhancer/silencer splicing
element motifs (Wang et al. 2005) do not have GQ/imGQ-folding potential, recent publications
suggest that GQ-like structures may influence splicing (Han et al. 2005; Fisette et al. 2012) and
that the genes that undergo alternative splicing are enriched with GQs (Kostadinov et al. 2006).
In conclusion, the broadened GQ-search algorithm opens up new opportunities in the prediction
of DNA/RNA structure and allows thorough analysis of all possible conformations adopted by
polynucleotides.
METHODS
The ON synthesis and purification, the MS analysis and the UV-melting, CD and rotational
relaxation time measurements were performed as previously described (Varizhuk et al. 2013).
For the analysis GQ/imGQ abundance and distribution in human genome, RefSeq genomic
sequences (http://www.ncbi.nlm.nih.gov/refseq/rsg/about/
) were used.
NMR studies
NMR samples were prepared at a concentration of ~0.1 mM in 0.6 ml H2O+D2O (10%) buffer
solution containing 20 mM Tris-HCl (pH 7.5) and 100 mM KCl and annealed (heated to 90 C for
3 minutes, then cooled quickly on ice) prior to spectral measurements to ensure unimolecular
quadruplex folding.
1
H-NMR spectra were recorded with Bruker AVANCE II 300 (300.1 MHz),
Bruker AMX III (400.1 MHz) and Bruker AVANCE II 600 (600.1 MHz) spectrometers. The
1
H
chemical shifts were referenced relative to an external standard - sodium 2,2-dimethyl-2-
silapentane-5-sulfonate (DSS). The spectra were recorded using presaturation or pulsed-field
gradient WATERGATE W5 pulse sequences (zgprsp and zggpw5 from the Bruker library,
respectively) for H
2
O suppression.
Molecular modeling
Ct1 GQ models 1 and 2 were created as follows. The starting positions of the GQ core atoms
were obtained from the PDB (139D and 2KQH). The core of every GQ was created using Swiss-
PDB Viewer. Then, loops were added step by step as described further by utilizing the SYBYL
8.0 molecular modeling package. To remove unfavorable van der Waals interactions, the models
were reoptimized after attaching each loop using SYBYL 8.0 and the Powell method with the
following parameters: Gasteiger-Hückel charges, TRIPOS force field, non-bonded cut-off
this version posted January 23, 2014. ; https://doi.org/10.1101/001990doi: bioRxiv preprint
