TR199802503A2 - Endojen gen aktivasyonu için hücrelerin optimizasyonu. - Google Patents

Endojen gen aktivasyonu için hücrelerin optimizasyonu.

Info

Publication number
TR199802503A2
TR199802503A2 TR1998/02503A TR9802503A TR199802503A2 TR 199802503 A2 TR199802503 A2 TR 199802503A2 TR 1998/02503 A TR1998/02503 A TR 1998/02503A TR 9802503 A TR9802503 A TR 9802503A TR 199802503 A2 TR199802503 A2 TR 199802503A2
Authority
TR
Turkey
Prior art keywords
cells
relates
expression
optimization
endogenous gene
Prior art date
Application number
TR1998/02503A
Other languages
English (en)
Other versions
TR199802503A3 (tr
Inventor
Honold Konrad
Holtschke Thomas
Stern Anne
Original Assignee
Boehringer Mannheim Gmbh
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8227717&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TR199802503(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Mannheim Gmbh filed Critical Boehringer Mannheim Gmbh
Publication of TR199802503A3 publication Critical patent/TR199802503A3/tr
Publication of TR199802503A2 publication Critical patent/TR199802503A2/tr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475Growth factors; Growth regulators
    • C07K14/505Erythropoietin [EPO]
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/65Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression using markers
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90Stable introduction of foreign DNA into chromosome
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90Stable introduction of foreign DNA into chromosome
    • C12N15/902Stable introduction of foreign DNA into chromosome using homologous recombination
    • C12N15/907Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian cells
    • 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
    • C12Q1/6897Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids involving reporter genes operably linked to promoters
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2800/00Nucleic acids vectors
    • C12N2800/30Vector systems comprising sequences for excision in presence of a recombinase, e.g. loxP or FRT
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2830/00Vector systems having a special element relevant for transcription
    • C12N2830/001Vector systems having a special element relevant for transcription controllable enhancer/promoter combination
    • C12N2830/002Vector systems having a special element relevant for transcription controllable enhancer/promoter combination inducible enhancer/promoter combination, e.g. hypoxia, iron, transcription factor

Landscapes

  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Physics & Mathematics (AREA)
  • Plant Pathology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Mycology (AREA)
  • Immunology (AREA)
  • Analytical Chemistry (AREA)
  • Cell Biology (AREA)
  • Toxicology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Medicinal Chemistry (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Bulus, hücrelerde gen sentezlemesinin optimize edilmesi için bir isleme iliskindir. Bulusun bir birinci yani, homolog rekombinasyon vasitasiyla hücrenin genomu içine bir heterolog sentezleme kontrol dizisinin verilmesinin yanisira girilen yabanci DNA' nin mevkiye-özgü rekombinaz-aracili kesilmesi ve daha baska heterolog sentezleme kontrol dizileri ve/ veya büyütme genleri ile degistirilmesiyle, bir ökariyotik hücrede endojen biçimde mevcut olan bir nükleik asit dizisinin sentezlenmesinin degistirilmesi için bir isleme iliskindir. Ilave olarak, bulus, bir aktivatör proteini ya da bir aktivatör protein kompleksinin baglandigi bir ya da bir kaç nükleik asit dizisinin, bir hedef genin sentezlenmesinin degistirilmesi amaciyla homolog rekombinasyon ile bir ökariyotik hücrenin genomu içine katilmasina dairdir.
TR1998/02503A 1997-12-01 1998-12-01 Endojen gen aktivasyonu için hücrelerin optimizasyonu. TR199802503A2 (tr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP97121075 1997-12-01

Publications (2)

Publication Number Publication Date
TR199802503A3 TR199802503A3 (tr) 1999-06-21
TR199802503A2 true TR199802503A2 (tr) 1999-06-21

Family

ID=8227717

Family Applications (1)

Application Number Title Priority Date Filing Date
TR1998/02503A TR199802503A2 (tr) 1997-12-01 1998-12-01 Endojen gen aktivasyonu için hücrelerin optimizasyonu.

Country Status (16)

Country Link
US (1) US7008764B1 (tr)
EP (3) EP1464705B1 (tr)
JP (1) JP4629813B2 (tr)
KR (1) KR100367062B1 (tr)
CN (2) CN1232644C (tr)
AR (4) AR018022A1 (tr)
AT (3) ATE360067T1 (tr)
AU (1) AU757930B2 (tr)
BR (1) BR9805682A (tr)
CA (1) CA2252970C (tr)
DE (3) DE59813438D1 (tr)
DK (3) DK0957165T3 (tr)
ES (3) ES2284228T3 (tr)
PT (3) PT919619E (tr)
TR (1) TR199802503A2 (tr)
ZA (1) ZA9810915B (tr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6316253B1 (en) 1999-11-01 2001-11-13 Chiron Corporation Expression vectors, transfection systems, and method of use thereof
CA2401677A1 (en) * 2000-03-03 2001-09-13 University Of Utah Research Foundation Gene targeting method
DE10023887A1 (de) * 2000-05-17 2001-11-29 Axel Haverich Verfahren zur transienten Insertion genetischer Elemente
WO2003012036A2 (en) 2001-07-27 2003-02-13 The Government Of The United States Of America As Represented By The Secretary Of Health And Human Services Systems for in vivo site-directed mutagenesis using oligonucleotides
WO2003087341A2 (en) 2002-01-23 2003-10-23 The University Of Utah Research Foundation Targeted chromosomal mutagenesis using zinc finger nucleases
EP2806025B1 (en) 2002-09-05 2019-04-03 California Institute of Technology Use of zinc finger nucleases to stimulate gene targeting
US8409861B2 (en) 2003-08-08 2013-04-02 Sangamo Biosciences, Inc. Targeted deletion of cellular DNA sequences
US20070134796A1 (en) * 2005-07-26 2007-06-14 Sangamo Biosciences, Inc. Targeted integration and expression of exogenous nucleic acid sequences
US11311574B2 (en) 2003-08-08 2022-04-26 Sangamo Therapeutics, Inc. Methods and compositions for targeted cleavage and recombination
US7888121B2 (en) 2003-08-08 2011-02-15 Sangamo Biosciences, Inc. Methods and compositions for targeted cleavage and recombination
US20120196370A1 (en) 2010-12-03 2012-08-02 Fyodor Urnov Methods and compositions for targeted genomic deletion
US7972854B2 (en) 2004-02-05 2011-07-05 Sangamo Biosciences, Inc. Methods and compositions for targeted cleavage and recombination
AU2005287278B2 (en) * 2004-09-16 2011-08-04 Sangamo Biosciences, Inc. Compositions and methods for protein production
CN103484496A (zh) * 2013-07-31 2014-01-01 新乡医学院 一种报告基因重组在染色体目的基因上的方法、位点及用途
US10006910B2 (en) 2014-12-18 2018-06-26 Agilome, Inc. Chemically-sensitive field effect transistors, systems, and methods for manufacturing and using the same
US10020300B2 (en) 2014-12-18 2018-07-10 Agilome, Inc. Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids
CA2971589C (en) 2014-12-18 2021-09-28 Edico Genome Corporation Chemically-sensitive field effect transistor
US9857328B2 (en) 2014-12-18 2018-01-02 Agilome, Inc. Chemically-sensitive field effect transistors, systems and methods for manufacturing and using the same
US9859394B2 (en) 2014-12-18 2018-01-02 Agilome, Inc. Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids
US9618474B2 (en) 2014-12-18 2017-04-11 Edico Genome, Inc. Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids
WO2017201081A1 (en) 2016-05-16 2017-11-23 Agilome, Inc. Graphene fet devices, systems, and methods of using the same for sequencing nucleic acids

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US568772A (en) * 1896-10-06 Albert s
CA1293460C (en) * 1985-10-07 1991-12-24 Brian Lee Sauer Site-specific recombination of dna in yeast
GB2187415A (en) 1986-03-05 1987-09-09 Deere & Co Machine for forming cylindrical bales of crop
JPS62265992A (ja) * 1986-05-12 1987-11-18 Ajinomoto Co Inc ヒト細胞を用いる有用物質の製造方法
US4956288A (en) * 1988-04-22 1990-09-11 Biogen, Inc. Method for producing cells containing stably integrated foreign DNA at a high copy number, the cells produced by this method, and the use of these cells to produce the polypeptides coded for by the foreign DNA
FR2646438B1 (fr) 1989-03-20 2007-11-02 Pasteur Institut Procede de remplacement specifique d'une copie d'un gene present dans le genome receveur par l'integration d'un gene different de celui ou se fait l'integration
EP0945515A3 (en) * 1989-11-06 2002-08-21 Cell Genesys, Inc. Production of proteins using homologous recombination
ES2151463T5 (es) * 1989-12-22 2012-10-29 Merck Serono Sa Constructos de ADN para la activación y la modificación de la expresión de genes endógenos
US5272071A (en) * 1989-12-22 1993-12-21 Applied Research Systems Ars Holding N.V. Method for the modification of the expression characteristics of an endogenous gene of a given cell line
WO1992015694A1 (en) * 1991-03-08 1992-09-17 The Salk Institute For Biological Studies Flp-mediated gene modification in mammalian cells, and compositions and cells useful therefor
US6270989B1 (en) * 1991-11-05 2001-08-07 Transkaryotic Therapies, Inc. Protein production and delivery
WO1993015191A1 (en) * 1992-01-24 1993-08-05 Life Technologies, Inc. Modulation of enzyme activities in the in vivo cloning of dna
TW402639B (en) * 1992-12-03 2000-08-21 Transkaryotic Therapies Inc Protein production and protein delivery
US5527695A (en) * 1993-01-29 1996-06-18 Purdue Research Foundation Controlled modification of eukaryotic genomes
ATE244311T1 (de) * 1993-12-23 2003-07-15 Merck & Co Inc Expressionssystem von antikörpern bei homologischer rekombinierung in murinezellen
US6130364A (en) * 1995-03-29 2000-10-10 Abgenix, Inc. Production of antibodies using Cre-mediated site-specific recombination
US5882914A (en) * 1995-06-06 1999-03-16 The Johns Hopkins University School Of Medicine Nucleic acids encoding the hypoxia inducible factor-1
US5695977A (en) * 1995-08-31 1997-12-09 Genetic Information Research Institute Site directed recombination
AUPN903196A0 (en) * 1996-03-29 1996-04-26 Australian National University, The Single-step excision means
US6020144A (en) * 1996-09-12 2000-02-01 Symbiontics, Inc. Sustained delivery device comprising a Leishmania protozoa and methods of making and using the same

Also Published As

Publication number Publication date
ES2258809T5 (es) 2013-09-05
ATE320491T1 (de) 2006-04-15
JPH11225785A (ja) 1999-08-24
AR020750A2 (es) 2002-05-29
CA2252970A1 (en) 1999-06-01
EP0919619B1 (de) 2006-03-01
PT919619E (pt) 2006-07-31
EP0919619A2 (de) 1999-06-02
AR020893A2 (es) 2002-06-05
PT957165E (pt) 2007-07-19
BR9805682A (pt) 2000-04-11
KR19990062655A (ko) 1999-07-26
CA2252970C (en) 2011-11-15
EP0957165A3 (de) 2000-10-04
JP4629813B2 (ja) 2011-02-09
DK0919619T4 (da) 2013-09-23
DK0957165T3 (da) 2007-07-30
AR020892A2 (es) 2002-06-05
DK1464705T3 (da) 2006-07-24
TR199802503A3 (tr) 1999-06-21
ES2259422T3 (es) 2006-10-01
AR018022A1 (es) 2001-10-31
DE59813413D1 (de) 2006-04-27
KR100367062B1 (ko) 2004-05-31
CN100519751C (zh) 2009-07-29
ATE318904T1 (de) 2006-03-15
AU9328498A (en) 1999-06-17
ATE360067T1 (de) 2007-05-15
DK0919619T3 (da) 2006-07-10
ES2284228T3 (es) 2007-11-01
ZA9810915B (en) 2000-05-30
ES2258809T3 (es) 2006-09-01
US7008764B1 (en) 2006-03-07
EP0957165B1 (de) 2007-04-18
PT1464705E (pt) 2006-08-31
EP0957165A2 (de) 1999-11-17
CN1590551A (zh) 2005-03-09
CN1240829A (zh) 2000-01-12
EP0919619A3 (de) 1999-07-21
DE59813976D1 (de) 2007-05-31
DE59813438D1 (de) 2006-05-11
EP1464705A1 (de) 2004-10-06
EP1464705B1 (de) 2006-03-15
EP0919619B2 (de) 2013-06-19
CN1232644C (zh) 2005-12-21
AU757930B2 (en) 2003-03-13

Similar Documents

Publication Publication Date Title
TR199802503A2 (tr) Endojen gen aktivasyonu için hücrelerin optimizasyonu.
US11713471B2 (en) Class II, type V CRISPR systems
Feng et al. Site-specific chromosomal integration in mammalian cells: highly efficient CRE recombinase-mediated cassette exchange
CN108559732A (zh) 基于CRISPR/Cas9靶向基因组修饰技术建立KI-T2A-luciferase细胞系的方法
DE60121372D1 (de) Methoden zur modifikation eukaryotischer zellen
CN111263810A (zh) 使用多核苷酸指导的核酸内切酶的细胞器基因组修饰
CA2203569A1 (en) Nucleotide sequence encoding the enzyme i-scei and the uses thereof
DE69935857D1 (de) Expression eukarotischer peptide in pflanzenplastiden
DE69738905D1 (de) Methoden und zusammensetzungen zur transformation von zellen
MX343591B (es) Métodos para modificar células eucarióticas.
ATE296356T1 (de) Methode zur spezifischen integration von genen in säugetierzellen durch homologe rekombination, und vektoren zu deren durchführung
CA2263958A1 (en) Homologous recombination in mismatch repair inactivated eukaryotic cells
CN107151677B (zh) 基于CRISPR/Cas9多基因敲除低转染效率细胞系的方法
CN110331146A (zh) 一种调控sgRNA转录的启动子、表达载体,及其基因组编辑系统和应用
PL326087A1 (en) Improved integration of exogenic dna introduced into eucariotic cells
Li et al. Genetic engineering in diatoms: advances and prospects
JP4158920B2 (ja) 耐熱性多頻度dna切断酵素の細胞内活性化によるゲノム再編成の誘発方法
JP2022512868A (ja) C2c1ヌクレアーゼに基づくゲノム編集のためのシステムおよび方法
US12241071B2 (en) Composition for editing flavonoid biosynthetic gene by using CRISPR/Cas9 system, and use thereof
Huang et al. Novel transgenic Chlamydomonas reinhardtii strain with retargetable genomic transgene integration using Cre-loxP system
EP1975228A1 (en) Polynucleotides for enhancing expression of a polynucleotide of interest
Kuhn et al. Complete sequence of the yeast artificial chromosome cloning vector pYAC4
Park et al. Reconstitution of mammalian excision repair activity with mutant cell-free extracts and XPAC and ERCC1 proteins expressed in Escherichia coli
RU2771374C1 (ru) Способы для бесшовного внесения целевых модификаций в направленные векторы
KR102302827B1 (ko) 크리스퍼 간섭을 이용한 유전자 발현 억제용 조성물