WO2012121486A3 - Sdl-pcr을 이용한 유전자 분석방법 - Google Patents

Sdl-pcr을 이용한 유전자 분석방법 Download PDF

Info

Publication number
WO2012121486A3
WO2012121486A3 PCT/KR2012/000695 KR2012000695W WO2012121486A3 WO 2012121486 A3 WO2012121486 A3 WO 2012121486A3 KR 2012000695 W KR2012000695 W KR 2012000695W WO 2012121486 A3 WO2012121486 A3 WO 2012121486A3
Authority
WO
WIPO (PCT)
Prior art keywords
pcr
sdl
ligation
probe
subjected
Prior art date
Application number
PCT/KR2012/000695
Other languages
English (en)
French (fr)
Other versions
WO2012121486A2 (ko
WO2012121486A9 (ko
Inventor
박현규
신성철
김가희
강병철
Original Assignee
한국과학기술원
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 한국과학기술원 filed Critical 한국과학기술원
Priority to US14/002,662 priority Critical patent/US9523117B2/en
Publication of WO2012121486A2 publication Critical patent/WO2012121486A2/ko
Publication of WO2012121486A9 publication Critical patent/WO2012121486A9/ko
Publication of WO2012121486A3 publication Critical patent/WO2012121486A3/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/6853Nucleic acid amplification reactions using modified primers or templates
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/6858Allele-specific amplification
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/6862Ligase chain reaction [LCR]
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2521/00Reaction characterised by the enzymatic activity
    • C12Q2521/50Other enzymatic activities
    • C12Q2521/501Ligase

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

본 발명은 SDL-PCR(Separation of displaced ligation probe-based PCR)을 이용한 유전자 분석방법에 관한 것으로, 보다 구체적으로, 목적 유전자와 상보적인 염기서열을 포함하는 각각의 탐침들을 리가제(ligase)를 이용하여 연결반응시키고, 상기 탐침과 혼성화될 수 있는 또 다른 탐침을 첨가하여 혼성화시킨다음 연장(extention)반응시켜 주형 탐침을 제조하고, 공통의 프라이머를 이용하여 목적유전자의 주형 탐침을 증폭시키는 것을 특징으로 하는 SDL-PCR을 이용한 유전자 분석방법에 관한 것이다. 본 발명에 따른 SDL-PCR 방법은 연결 반응이 되지 않은 미반응 탐침 또는 genomic DNA를 태그를 이용하여 제거함으로써, 비특이적 증폭 반응을 최소화할 수 있을 뿐만 아니라 exonuclease를 이용하는 정제방법보다 빠른 시간 내에 정제가 가능하며 단일 튜브 내의 동일 용액에서 연결, 정제 및 중합효소연쇄반응이 가능하여 정확하고 신속하게 복수의 유전자를 동시에 증폭시킬 수 있다.
PCT/KR2012/000695 2011-03-04 2012-01-30 Sdl-pcr을 이용한 유전자 분석방법 WO2012121486A2 (ko)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US14/002,662 US9523117B2 (en) 2011-03-04 2012-01-30 Gene analysis method using SDL-PCR

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2011-0019225 2011-03-04
KR1020110019225A KR101322880B1 (ko) 2011-03-04 2011-03-04 Sdl-pcr을 이용한 유전자 분석방법

Publications (3)

Publication Number Publication Date
WO2012121486A2 WO2012121486A2 (ko) 2012-09-13
WO2012121486A9 WO2012121486A9 (ko) 2012-10-18
WO2012121486A3 true WO2012121486A3 (ko) 2012-12-20

Family

ID=46798615

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2012/000695 WO2012121486A2 (ko) 2011-03-04 2012-01-30 Sdl-pcr을 이용한 유전자 분석방법

Country Status (3)

Country Link
US (1) US9523117B2 (ko)
KR (1) KR101322880B1 (ko)
WO (1) WO2012121486A2 (ko)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG194745A1 (en) * 2011-05-20 2013-12-30 Fluidigm Corp Nucleic acid encoding reactions
CN105803055A (zh) * 2014-12-31 2016-07-27 天昊生物医药科技(苏州)有限公司 一种基于多重循环延伸连接的靶基因区域富集新方法
US11117113B2 (en) 2015-12-16 2021-09-14 Fluidigm Corporation High-level multiplex amplification

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030082584A1 (en) * 2001-06-29 2003-05-01 Liang Shi Enzymatic ligation-based identification of transcript expression
WO2009140802A1 (zh) * 2008-05-23 2009-11-26 陕西北美基因股份有限公司 检测探针、通用寡核苷酸芯片及核酸检测方法及其用途
US20100267585A1 (en) * 2009-04-01 2010-10-21 Dxterity Diagnostics Chemical ligation dependent probe amplification (CLPA)

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1130113A1 (en) * 2000-02-15 2001-09-05 Johannes Petrus Schouten Multiplex ligation dependent amplification assay
WO2003060163A2 (en) * 2001-12-28 2003-07-24 Keygene N.V. Discrimination and detection of target nucleotide sequences using mass spectrometry
EP1664345B1 (en) * 2003-09-02 2015-04-01 Keygene N.V. Ola-based methods for the detection of target nucleic acid sequences
US20050266417A1 (en) * 2003-09-12 2005-12-01 Francis Barany Methods for identifying target nucleic acid molecules
US8580494B2 (en) * 2006-08-25 2013-11-12 Research Foundation For Mental Hygiene, Inc. Methods and compositions for amplification and detection of MicroRNAs
WO2008069906A2 (en) * 2006-11-14 2008-06-12 The Regents Of The University Of California Digital expression of gene analysis
WO2011102802A1 (en) * 2010-02-18 2011-08-25 Agency For Science, Technology And Research Method for reducing mismatches in double-stranded dna molecules

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030082584A1 (en) * 2001-06-29 2003-05-01 Liang Shi Enzymatic ligation-based identification of transcript expression
WO2009140802A1 (zh) * 2008-05-23 2009-11-26 陕西北美基因股份有限公司 检测探针、通用寡核苷酸芯片及核酸检测方法及其用途
US20100267585A1 (en) * 2009-04-01 2010-10-21 Dxterity Diagnostics Chemical ligation dependent probe amplification (CLPA)

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ASARI, M. ET AL.: "Enhanced discrimination of single nucleotide polymorphisms using 3' nucleotide differences in ligase detection reaction probes", MOLECULAR AND CELLULAR PROBES, vol. 24, 24 August 2010 (2010-08-24), pages 381 - 386 *
CARNEVALE, E. P. ET AL.: "A multiplex ligase detection reaction-fluorescent microsphere assay for simultaneous detection of single nucleotide polymorphisms associated with Plasmodium falciparum drug resistance", JOURNAL OF CLINICAL MICROBIOLOGY, vol. 45, no. 3, March 2007 (2007-03-01), pages 752 - 761 *

Also Published As

Publication number Publication date
KR101322880B1 (ko) 2013-10-29
WO2012121486A2 (ko) 2012-09-13
US9523117B2 (en) 2016-12-20
US20140171334A1 (en) 2014-06-19
WO2012121486A9 (ko) 2012-10-18
KR20120101255A (ko) 2012-09-13

Similar Documents

Publication Publication Date Title
JP2015156872A5 (ko)
HRP20161056T1 (hr) Metode za odabir i umnožavanje polinukleotida
WO2013003630A3 (en) Methods and compositions for enrichment of nucleic acids in mixtures of highly homologous sequences
WO2005089508A3 (en) Dna sequence detection by limited primer extension
IL300974A (en) Preparations and methods for the detection of rare sequence variants
NZ616407A (en) Method and product for localised or spatial detection of nucleic acid in a tissue sample
RU2012129362A (ru) Обнаружение мишени tsg праймером
WO2010083250A3 (en) Single-cell nucleic acid analysis
GB2470672A (en) Methods of RNA aplification in the presence of DNA
JP2015521468A5 (ko)
NZ608313A (en) Direct capture, amplification and sequencing of target dna using immobilized primers
ATE550441T1 (de) Verfahren, zusammensetzungen und kits zur isothermischen amplifikation von nukleinsäuren
JP2011502502A5 (ko)
WO2009140802A8 (zh) 检测探针、通用寡核苷酸芯片及核酸检测方法及其用途
GB2595076A (en) Methods for targeted nucleic acid library formation
JP2013509871A5 (ko)
JP2014083053A5 (ko)
HRP20200321T1 (hr) Detekcija ciljne nukleinske kiseline i varijanti
NZ594155A (en) Methods for amplifying hepatitis c virus nucleic acids
JP2012514451A5 (ko)
JP2011101652A5 (ko)
GB2445529A (en) Method for isothermal amplification of nucleic acids and method for detecting nucleic acids using simultaneous isothermal amplification of nucleic acids
WO2011140187A3 (en) Detecting chromosomal rearrangement
WO2016059473A3 (en) Sequence conversion and signal amplifier dna having locked nucleic acids and detection methods using same
JP2017530715A5 (ko)

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12755650

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 14002662

Country of ref document: US

122 Ep: pct application non-entry in european phase

Ref document number: 12755650

Country of ref document: EP

Kind code of ref document: A2