Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

DNA mutation motifs in the genes associated with inherited diseases

M. Růžička, P. Kulhánek, L. Radová, A. Čechová, N. Špačková, L. Fajkusová, K. Réblová,

. 2017 ; 12 (8) : e0182377. [pub] 20170802

Language English Country United States

Document type Journal Article

Mutations in human genes can be responsible for inherited genetic disorders and cancer. Mutations can arise due to environmental factors or spontaneously. It has been shown that certain DNA sequences are more prone to mutate. These sites are termed hotspots and exhibit a higher mutation frequency than expected by chance. In contrast, DNA sequences with lower mutation frequencies than expected by chance are termed coldspots. Mutation hotspots are usually derived from a mutation spectrum, which reflects particular population where an effect of a common ancestor plays a role. To detect coldspots/hotspots unaffected by population bias, we analysed the presence of germline mutations obtained from HGMD database in the 5-nucleotide segments repeatedly occurring in genes associated with common inherited disorders, in particular, the PAH, LDLR, CFTR, F8, and F9 genes. Statistically significant sequences (mutational motifs) rarely associated with mutations (coldspots) and frequently associated with mutations (hotspots) exhibited characteristic sequence patterns, e.g. coldspots contained purine tract while hotspots showed alternating purine-pyrimidine bases, often with the presence of CpG dinucleotide. Using molecular dynamics simulations and free energy calculations, we analysed the global bending properties of two selected coldspots and two hotspots with a G/T mismatch. We observed that the coldspots were inherently more flexible than the hotspots. We assume that this property might be critical for effective mismatch repair as DNA with a mutation recognized by MutSα protein is noticeably bent.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17030659
003      
CZ-PrNML
005      
20171025122716.0
007      
ta
008      
171025s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1371/journal.pone.0182377 $2 doi
035    __
$a (PubMed)28767725
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Růžička, Michal $u CEITEC-Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, Czech Republic. Department of Condensed Matter Physics, Faculty of Science, Masaryk University, Kotlářská 2, Brno, Czech Republic.
245    10
$a DNA mutation motifs in the genes associated with inherited diseases / $c M. Růžička, P. Kulhánek, L. Radová, A. Čechová, N. Špačková, L. Fajkusová, K. Réblová,
520    9_
$a Mutations in human genes can be responsible for inherited genetic disorders and cancer. Mutations can arise due to environmental factors or spontaneously. It has been shown that certain DNA sequences are more prone to mutate. These sites are termed hotspots and exhibit a higher mutation frequency than expected by chance. In contrast, DNA sequences with lower mutation frequencies than expected by chance are termed coldspots. Mutation hotspots are usually derived from a mutation spectrum, which reflects particular population where an effect of a common ancestor plays a role. To detect coldspots/hotspots unaffected by population bias, we analysed the presence of germline mutations obtained from HGMD database in the 5-nucleotide segments repeatedly occurring in genes associated with common inherited disorders, in particular, the PAH, LDLR, CFTR, F8, and F9 genes. Statistically significant sequences (mutational motifs) rarely associated with mutations (coldspots) and frequently associated with mutations (hotspots) exhibited characteristic sequence patterns, e.g. coldspots contained purine tract while hotspots showed alternating purine-pyrimidine bases, often with the presence of CpG dinucleotide. Using molecular dynamics simulations and free energy calculations, we analysed the global bending properties of two selected coldspots and two hotspots with a G/T mismatch. We observed that the coldspots were inherently more flexible than the hotspots. We assume that this property might be critical for effective mismatch repair as DNA with a mutation recognized by MutSα protein is noticeably bent.
650    _2
$a protein CFTR $x genetika $7 D019005
650    _2
$a DNA $x chemie $x genetika $7 D004247
650    _2
$a faktor VIII $x genetika $7 D005169
650    _2
$a genetická predispozice k nemoci $7 D020022
650    12
$a zárodečné mutace $7 D018095
650    _2
$a lidé $7 D006801
650    _2
$a molekulární modely $7 D008958
650    _2
$a simulace molekulární dynamiky $7 D056004
650    _2
$a konformace nukleové kyseliny $7 D009690
650    _2
$a nukleotidové motivy $7 D059372
650    _2
$a LDL-receptory $x genetika $7 D011973
655    _2
$a časopisecké články $7 D016428
700    1_
$a Kulhánek, Petr $u CEITEC-Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, Czech Republic. National Centre for Biomolecular Research, Faculty of Science, Masaryk University, Kamenice 5, Brno, Czech Republic.
700    1_
$a Radová, Lenka $u CEITEC-Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, Czech Republic.
700    1_
$a Čechová, Andrea $u CEITEC-Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, Czech Republic.
700    1_
$a Špačková, Naďa $u Department of Condensed Matter Physics, Faculty of Science, Masaryk University, Kotlářská 2, Brno, Czech Republic.
700    1_
$a Fajkusová, Lenka $u Centre of Molecular Biology and Gene Therapy, University Hospital Brno and Masaryk University, Jihlavská 20, Brno, Czech Republic.
700    1_
$a Réblová, Kamila $u CEITEC-Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, Czech Republic.
773    0_
$w MED00180950 $t PloS one $x 1932-6203 $g Roč. 12, č. 8 (2017), s. e0182377
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28767725 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20171025 $b ABA008
991    __
$a 20171025122758 $b ABA008
999    __
$a ok $b bmc $g 1254252 $s 991686
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 12 $c 8 $d e0182377 $e 20170802 $i 1932-6203 $m PLoS One $n PLoS One $x MED00180950
LZP    __
$a Pubmed-20171025

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...