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AR107621A2 - Plantas de algodón con tolerancia a herbicidas y métodos para identificarlas - Google Patents

Plantas de algodón con tolerancia a herbicidas y métodos para identificarlas

Info

Publication number
AR107621A2
AR107621A2 ARP170100365A ARP170100365A AR107621A2 AR 107621 A2 AR107621 A2 AR 107621A2 AR P170100365 A ARP170100365 A AR P170100365A AR P170100365 A ARP170100365 A AR P170100365A AR 107621 A2 AR107621 A2 AR 107621A2
Authority
AR
Argentina
Prior art keywords
nucleotide
seq
elite event
nucleotide sequence
nucleotides
Prior art date
Application number
ARP170100365A
Other languages
English (en)
Inventor
Veerle Habex
Linda Trolinder
Original Assignee
Bayer Cropscience Nv
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 Bayer Cropscience Nv filed Critical Bayer Cropscience Nv
Publication of AR107621A2 publication Critical patent/AR107621A2/es

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    • 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
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • 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
    • C12N15/82Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
    • C12N15/8271Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance
    • C12N15/8274Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for herbicide resistance
    • C12N15/8275Glyphosate

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Cell Biology (AREA)
  • Plant Pathology (AREA)
  • Immunology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

Reivindicación 1: Un método para identificar un evento de elite en una muestra de una planta, un material vegetal, una semilla o un producto que comprende dicho material vegetal, caracterizado porque dicho método comprende amplificar la secuencia blanco de dicho evento de elite entre 100 y 500 bp a partir de un ácido nucleico presente en dichas muestras de una planta, un material vegetal, una semilla o un producto que comprende dicho material vegetal, usando una reacción en cadena de la polimerasa con dos cebadores, donde uno de dichos cebadores reconoce la región circundante 5’ de EE-GH3, donde dicha región circundante 5’ tiene la secuencia de nucleótidos de SEQ ID Nº 1, desde el nucleótido 1 hasta el nucleótido 732, o la región circundante 3’ de EE-GH3, donde dicha región circundante 3’ tiene la secuencia de nucleótidos del complemento de SEQ ID Nº 2, desde el nucleótido 431 hasta el nucleótido 654, y el otro cebador de dicho par de cebadores reconoce una secuencia dentro del transgen que tiene la secuencia de nucleótidos del complemento de SEQ ID Nº 1, desde el nucleótido 733 hasta el nucleótido 1214, o la secuencia de nucleótidos de SEQ ID Nº 2, desde el nucleótido 1 hasta el nucleótido 430, en donde dicho evento de elite comprende: un transgén que comprende un gen quimérico que comprende una enzima 5-enol-piruvilshikimato-3-fosfato sintetasa (EPSPD) tolerante al glifosato como se describe en la patente US 6,566,587, bajo el control de un promotor de un gen de histonas como se describe en US 5,491,288 o US 5,792,930; SEQ ID Nº 1, donde los nucleótidos 1 - 732 de SEQ ID Nº 1 están inmediatamente aguas arriba de y contiguos con dicho transgén y los nucleótidos 733 - 1214 de SEQ ID Nº 1 son ADN del transgén; SEQ ID Nº 2, donde los nucleótidos 431 - 654 de SEQ ID Nº 2 están inmediatamente aguas debajo de y contiguos con dicho transgén, y los nucleótidos 1 a 430 de SEQ ID Nº 2 son ADN del transgén; donde dicho evento de elite está presente en semillas que han sido depositadas en la ATCC bajo el número de depósito PTA-6878. Reivindicación 5: Un par de moléculas aisladas de ADN que es un cebador adecuado para su uso en la detección de un evento de elite de acuerdo con la reivindicación 1, caracterizado porque una molécula de ADN comprende en su extremo 3’ una secuencia de nucleótidos de 17 nucleótidos consecutivos seleccionados de la secuencia de nucleótidos de SEQ ID Nº 1, desde el nucleótido 1 hasta el nucleótido 732, o una secuencia de nucleótidos de 17 nucleótidos consecutivos seleccionados de la secuencia de nucleótidos del complemento de SEQ ID Nº 2, desde el nucleótido 431 hasta el nucleótido 654, en donde una molécula de ADN comprende en su extremo 3’ una secuencia de nucleótidos de 17 nucleótidos consecutivos seleccionados de la secuencia de nucleótidos del complemento de SEQ ID Nº 1, desde el nucleótido 733 hasta el nucleótido 1214,o la secuencia de nucleótidos de 17 nucleótidos consecutivos seleccionados de la secuencia de nucleótidos de SEQ ID Nº 2, desde el nucleótido 1 hasta el nucleótido 430, en donde al menos uno de dichos cebadores está marcado. Reivindicación 10: Un método para confirmar la pureza de semillas, caracterizado porque dicho método comprende la detección de una región específica para el evento de elite de acuerdo con la reivindicación 1, con un cebador o una sonda específica, que reconoce específicamente la región circundante 5’ o 3’ de dicho evento de elite, en muestras de semillas. Reivindicación 12: Un método para determinar el estado de cigosidad de una planta, un material vegetal o una semilla que comprende el evento elite de acuerdo con la reivindicación 1, caracterizado porque dicho método comprende amplificar la secuencia blanco de dicho evento de elite entre 100 y 500 bp a partir de un ácido nucleico presente en dicha planta, material vegetal o semilla, usando una reacción. en cadena de la polimerasa con tres cebadores, donde uno de dichos cebadores reconoce la región circundante 5’ de dicho evento de elite, donde dicha región circundante 5’ tiene la secuencia de nucleótidos de SEQ ID Nº 1, desde el nucleótido 1 hasta el nucleótido 732, el segundo de dichos cebadores reconoce específicamente la región circundante 3’ de dicho evento de elite, donde dicha región circundante 3’ tiene la secuencia de nucleótidos del complemento de SEQ ID Nº 2, desde el nucleótido 431 hasta el nucleótido 654, y el tercero de dichos cebadores reconoce una secuencia dentro del transgen que tiene la secuencia de nucleótidos del complemento de SEQ ID Nº 1, desde el nucleótido 733 hasta el nucleótido 1214, o la secuencia de nucleótidos de SEQ ID Nº 2, desde el nucleótido 1 hasta el nucleótido 430. Reivindicación 15: Un método para producir una planta o una semilla de algodón resistente a glifosato que comprende el evento elite EE-GH3, caracterizado porque dicho método comprende introducir una molécula de ADN recombinante, donde dicha molécula de ADN recombinante comprende un gen quimérico que comprende una enzima 5-enol-piruvilshikimato-3-fosfato sintetasa (EPSPD) tolerante al glifosato como se describe en la patente US 6,566,587, bajo el control de un promotor de un gen de histonas como se describe en US 5,491,288 o US 5,792,930, en una región del ADN cromosomal de algodón que comprende la secuencia SEQ ID Nº 1, nucleótidos 1 - 732 y SEQ ID Nº 2, nucleótidos 431 - 654, mediante el cruzamiento de plantas que poseen dicho evento elite en el genoma, y sembrar la semilla obtenida a partir de dicho cruzamiento y tratar las plantas en crecimiento con glifosato, donde dicho evento elite comprende dicha molécula de ADN recombinante integrado en el ADN cromosomal, y donde los nucleótidos 1 - 732 de SEQ ID Nº 1 están inmediatamente aguas arriba de y contiguos con dicho ADN recombinante y donde los nucleótidos 733 - 1214 de SEQ ID Nº 1 son ADN recombinante, y donde los nucleótidos 431 - 654 de SEQ ID Nº 2 están inmediatamente aguas abajo de y contiguos con dicho ADN recombinante, y donde los nucleótidos 1 a 430 de SEQ ID Nº 2 son ADN recombinante, y donde dichas plantas que poseen un evento elite se obtienen de las semillas que han sido depositadas en la ATCC bajo el número de deposito PTA-6878.
ARP170100365A 2005-08-08 2017-02-15 Plantas de algodón con tolerancia a herbicidas y métodos para identificarlas AR107621A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05076826 2005-08-08

Publications (1)

Publication Number Publication Date
AR107621A2 true AR107621A2 (es) 2018-05-16

Family

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Family Applications (2)

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ARP060103443A AR054901A1 (es) 2005-08-08 2006-08-08 Plantas de algodon con tolerancia a herbicidas y metodos para identificarlas
ARP170100365A AR107621A2 (es) 2005-08-08 2017-02-15 Plantas de algodón con tolerancia a herbicidas y métodos para identificarlas

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Country Status (10)

Country Link
US (3) US7932439B2 (es)
EP (2) EP1922409B1 (es)
CN (1) CN101238217B (es)
AR (2) AR054901A1 (es)
AU (1) AU2006278778B2 (es)
BR (1) BRPI0614338B1 (es)
ES (1) ES2654294T3 (es)
MX (1) MX2008001839A (es)
WO (1) WO2007017186A1 (es)
ZA (1) ZA200800909B (es)

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