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

Application of nonsense-mediated primer exclusion (NOPE) for preparation of unique molecular barcoded libraries

DA. Shagin, MA. Turchaninova, IA. Shagina, M. Shugay, AR. Zaretsky, OI. Zueva, DA. Bolotin, S. Lukyanov, DM. Chudakov,

. 2017 ; 18 (1) : 440. [pub] 20170605

Language English Country Great Britain

Document type Journal Article, Research Support, Non-U.S. Gov't

BACKGROUND: Recently we proposed efficient method to exclude undesirable primers at any stage of amplification reaction, here termed NOPE (NOnsense-mediated Primer Exclusion). According to this method, added oligonucleotide overlapping with the 3'-end of unwanted amplification primer (NOPE oligo) simultaneously provides a template for its elongation. This elongation disrupts specificity of unwanted primer, preventing its further participation in PCR. The suggested approach allows to rationally manage the course of PCR reactions in order to facilitate analysis of complex DNA mixtures as well as to perform multistage PCR bypassing intermediate purification steps. RESULTS: Here we apply NOPE method to DNA library preparation for the high-throughput sequencing (HTS) with the PCR-based introduction of unique molecular identifiers (UMI). We show that NOPE oligo efficiently neutralizes UMI-containing oligonucleotides after introduction of UMI into sample DNA molecules, thus allowing to proceed with further amplification steps without purification and associated loss of starting material. At the same time, NOPE oligo does not affect the efficiency of target PCR amplification. CONCLUSION: We describe a simple, robust and cheap modification of UMI-labeled HTS libraries preparation procedure, that allows to bypass purification step and thus to preserve starting material which may be limited, e.g. circulating tumor DNA, circulating fetal DNA, or small amounts of isolated cells of interest. Furthermore, demonstrated simplicity and robustness of NOPE method should make it popular in various PCR protocols.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18010517
003      
CZ-PrNML
005      
20180418095612.0
007      
ta
008      
180404s2017 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/s12864-017-3815-2 $2 doi
035    __
$a (PubMed)28583065
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Shagin, Dmitriy A $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia.
245    10
$a Application of nonsense-mediated primer exclusion (NOPE) for preparation of unique molecular barcoded libraries / $c DA. Shagin, MA. Turchaninova, IA. Shagina, M. Shugay, AR. Zaretsky, OI. Zueva, DA. Bolotin, S. Lukyanov, DM. Chudakov,
520    9_
$a BACKGROUND: Recently we proposed efficient method to exclude undesirable primers at any stage of amplification reaction, here termed NOPE (NOnsense-mediated Primer Exclusion). According to this method, added oligonucleotide overlapping with the 3'-end of unwanted amplification primer (NOPE oligo) simultaneously provides a template for its elongation. This elongation disrupts specificity of unwanted primer, preventing its further participation in PCR. The suggested approach allows to rationally manage the course of PCR reactions in order to facilitate analysis of complex DNA mixtures as well as to perform multistage PCR bypassing intermediate purification steps. RESULTS: Here we apply NOPE method to DNA library preparation for the high-throughput sequencing (HTS) with the PCR-based introduction of unique molecular identifiers (UMI). We show that NOPE oligo efficiently neutralizes UMI-containing oligonucleotides after introduction of UMI into sample DNA molecules, thus allowing to proceed with further amplification steps without purification and associated loss of starting material. At the same time, NOPE oligo does not affect the efficiency of target PCR amplification. CONCLUSION: We describe a simple, robust and cheap modification of UMI-labeled HTS libraries preparation procedure, that allows to bypass purification step and thus to preserve starting material which may be limited, e.g. circulating tumor DNA, circulating fetal DNA, or small amounts of isolated cells of interest. Furthermore, demonstrated simplicity and robustness of NOPE method should make it popular in various PCR protocols.
650    _2
$a DNA primery $x genetika $7 D017931
650    12
$a genová knihovna $7 D015723
650    _2
$a vysoce účinné nukleotidové sekvenování $7 D059014
650    _2
$a polymerázová řetězová reakce $x metody $7 D016133
650    _2
$a erbB receptory $x genetika $7 D066246
650    _2
$a sekvenční analýza DNA $7 D017422
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Turchaninova, Maria A $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia. Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
700    1_
$a Shagina, Irina A $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia.
700    1_
$a Shugay, Mikhail $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia. Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
700    1_
$a Zaretsky, Andrew R $u Pirogov Russian National Research Medical University, Moscow, Russia. Evrogen JSC, Moscow, Russia.
700    1_
$a Zueva, Olga I $u Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia.
700    1_
$a Bolotin, Dmitriy A $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia.
700    1_
$a Lukyanov, Sergey $u Pirogov Russian National Research Medical University, Moscow, Russia. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia.
700    1_
$a Chudakov, Dmitriy M $u Pirogov Russian National Research Medical University, Moscow, Russia. chudakovdm@mail.ru. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, Russia. chudakovdm@mail.ru. Central European Institute of Technology, Masaryk University, Brno, Czech Republic. chudakovdm@mail.ru. Skolkovo Institute of Science and Technology, Moscow, Russia. chudakovdm@mail.ru.
773    0_
$w MED00008181 $t BMC genomics $x 1471-2164 $g Roč. 18, č. 1 (2017), s. 440
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28583065 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180404 $b ABA008
991    __
$a 20180418095712 $b ABA008
999    __
$a ok $b bmc $g 1288002 $s 1007329
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 18 $c 1 $d 440 $e 20170605 $i 1471-2164 $m BMC genomics $n BMC Genomics $x MED00008181
LZP    __
$a Pubmed-20180404

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...