WO1998056811B1 - Plant grab proteins - Google Patents

Plant grab proteins

Info

Publication number
WO1998056811B1
WO1998056811B1 PCT/EP1998/003662 EP9803662W WO9856811B1 WO 1998056811 B1 WO1998056811 B1 WO 1998056811B1 EP 9803662 W EP9803662 W EP 9803662W WO 9856811 B1 WO9856811 B1 WO 9856811B1
Authority
WO
WIPO (PCT)
Prior art keywords
grab
peptide
protein
seq
sequence
Prior art date
Application number
PCT/EP1998/003662
Other languages
French (fr)
Other versions
WO1998056811A3 (en
WO1998056811A2 (en
WO1998056811A8 (en
Inventor
Crisanto Gutierrez-Armenta
Xie Qi
Andres Sanz-Burgos
Original Assignee
Consejo Superior Investigacion
Gutierrez Armenta Crisanto
Xie Qi
Sanz Burgos Andres
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 Consejo Superior Investigacion, Gutierrez Armenta Crisanto, Xie Qi, Sanz Burgos Andres filed Critical Consejo Superior Investigacion
Priority to CA002289863A priority Critical patent/CA2289863A1/en
Priority to AU82160/98A priority patent/AU753798B2/en
Priority to BR9809447-5A priority patent/BR9809447A/en
Priority to NZ500529A priority patent/NZ500529A/en
Priority to EP98932162A priority patent/EP0989997A2/en
Priority to JP50164599A priority patent/JP2002506345A/en
Publication of WO1998056811A2 publication Critical patent/WO1998056811A2/en
Publication of WO1998056811A3 publication Critical patent/WO1998056811A3/en
Publication of WO1998056811B1 publication Critical patent/WO1998056811B1/en
Publication of WO1998056811A8 publication Critical patent/WO1998056811A8/en

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/415Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
    • 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
    • C12N15/8279Phenotypically 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 biotic stress resistance, pathogen resistance, disease resistance
    • C12N15/8283Phenotypically 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 biotic stress resistance, pathogen resistance, disease resistance for virus resistance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/146Genetically Modified [GMO] plants, e.g. transgenic plants

Abstract

A method of controlling plant cell and plant virus growth and/or replication, plant cell cycle, differentiation, development and/or scenescence is provided characterised in that it comprises increasing or decreasing the levels or binding capabilities of GRAB (Geminivirus RepA Binding) proteins other than Rb (Retinoblastoma) proteins within plant cells.

Claims

AMENDED CLAIMS[received by the International Bureau on 22 February 1999 (22.02.99); original claims 1-33 replaced by amended claims 1-32 (6 pages)]
1. A method of controlling plant cell cycle characterised in that it comprises increasing or decreasing the levels of, or Geminivirus RepA binding capabilities of, GRAB (Geminivirus RepA Binding) protein or peptide within a plant cell characterised in that the GRAB protein or peptide comprises domains Nl, N2, N3, N4 and N5 shown in Figure 5 herein which have the designated amino acids shown in SEQ ID No 3 and SEQ ID 4.
2. A method as claimed in claim 1 characterised in that the control of the plant cell cycle comprises one or more of control of plant cell or plant virus growth and/or replication, plant cell differentiation, development and/or scenescence.
3. A method as claimed in any one of the preceding claims wherein the GRAB proteins or peptides have a first 150 N-terminal amino acids capable of binding to viral
RepA protein.
4. A method as claimed in any one of the preceding claims characterised in that the GRAB proteins or peptide comprises an amino acid sequence SEQ ID No 3 or 4 as shown herein or a functional variant thereof that is capable of binding Geminivirus RepA.
5. A method as claimed in any one of the preceding claims characterised in that it comprises overproducing or underproducing the protein or peptide in a plant cell.
51
6. A method as claimed in any one of claims 1 to 5 characterised in that it comprises decrease of native GRAB binding activity by application of an agent that binds to GRAB protein or peptide.
7. A method as claimed in any one of the preceding claims characterised in that the GRAB proteins or peptides have amino acid sequence homology of at least 70% with that of SEQ ID No 3 or 4.
8. A method as claimed in any one of the preceding claims comprising placing of the corresponding GRAB protein or peptide encoding or antisense nucleotides within the plant cell.
9. A method as claimed in claim 8 characterised in that the nucleotides are in the form of recombinant nucleic acid comprising a GRAB protein or peptide encoding sequence.
10. A method as claimed in claim 9 characterised in that the sequence is positioned behind a promotor capable of supporting GRAB protein or peptide expression or production of antisense RN A.
1 1 . A method as claimed in any one of claims 1 to 10 characterised in that the protein or peptide is applied or produced ectopically.
52
12. A method as claimed in claim 1 1 characterised in that the tissue is vegetative tissue or stem tissue.
13. A method as claimed in any one of the preceding claims comprising expressing a protein or peptide that is capable of binding to GRAB protein or peptide or functional variant thereof within the cell.
14. A method as claimed in any preceding claim characterised in that it comprises downregulating native GRAB expression by gene silencing coexpression or through antisense strategy.
15. A method as claimed in any one of the preceding claims characterised in that it comprises producing or inhibiting senescence in a plant cell comprising increasing or decreasing the levels or binding activity of a GRAB protein or peptide comprising a sequence of SEQ ID No 10 or a functional variant therof capable of inducing senescence in N.bentamiana plants, in a plant cell.
16. A method as claimed in claim 15 comprising incorporation of nucleic acid encoding RepA, N-terminal truncated RepA or a functional variant of one of these.
17. A GRAB protein or peptide per se, or in enriched, isolated, cell free and/or recombinantly produced form characterised in that characterised in that the GRAB protein or peptide comprises domains Nl , N2, N3, N4 and N5 shown in Figure 5 herein which have the designated amino acids shown in SEQ ID No 3 and SEQ ID 4 and with the proviso that it is not one of SENU, NAM, ATAF 1 or ATAF2.
18. A protein or peptide as claimed in claim 17 characterised in it has an N-terminal sequence having 90% or more homology to the first 150 N-terminal amino acids of GRAB 1 or GRAB2 described herein or conservatively substituted variants thereof.
19. A GRAB protein or peptide as claimed in claim 17 characterised in that it comprises an amino acid sequence SEQ ID No 3 or 4 as shown or a functional variant thereof having an amino acid sequence of homology of at least 70% with that sequence that is capable of binding Geminivirus RepA.
20. A protein or peptide as claimed in claim 19 characterised in that it comprises a sequence of SEQ ID No 6 or 8 or a functional variant thereof having an amino acid sequence of homology of at least 70% with that sequence.
21. A protein or peptide as claimed in claim 20 characterised in that it comprises a sequence of SEQ ID No 10 or 12 or a functional variant thereof having an amino acid sequence of homology of at least 70% with that sequence.
22. A GRAB protein or peptide encoding or antisense nucleic acid per se, or in enriched, isolated, cell free and/or recombinant form characterised in that the GRAB protein or peptide comprises domains Nl . N2, N3. N4 and N5 shown in Figure 5 herein which have the designated amino acids shown in SEQ ID No 3 and SEQ ID 4 and with the proviso that it does not encode the full amino acid sequence of SENU, NAM, ATAF1 or ATAF2.
23. Nucleic acid as claimed in claim 22 characterised in that it is in the form of recombinant DNA or cRNA (mRNA) that codes for the expression of a GRAB protein or peptide having an N-terminal sequence with at least 60% homology with the first 200 N-terminal amino acids of GRAB 1 or GRAB2 as described herein
54
24. A nucleic acid as claimed in claim 23 characterised in that it is a DNA or RNA polynucleotide comprising one or more of SEQ ID No 1, 2, 5, 7, 9 or 1 1 or a functional variant thereof
25. A method of producing a protein or peptide as claimed in any one of claims 18 to 23 characterised in that it comprises expressing DNA or RNA as described in claim 23 or 24.
26. A nucleic acid probe or primer characterised in that it comprises an oligonucleotide or polynucleotide of sequence complementary to any 15 or more contiguous bases of the DNA sequences identified herein below as SEQ ID No 5, 7, 9 or 1 1 or complemetary sequences or RNA sequences corresponding thereto.
27. A nucleic acid transformation vector characterised in that it comprises DNA or RNA as described in any one of claims 8 to 16 or 22 to 24.
28. A method for producing transformed cells comprising nucleic acid as claimed in or described in any one of claims 8 to 16 or 22 to 24 comprising introducing said nucleic acid into the cell in vector or free form.
29. A method as claimed in claim 28 characterised in that the nucleic acid is introduced directly by electroporation or particle bombardment.
30. A cell comprising recombinant nucleic acid as described or claimed in any one of claims 8 to 16 or 22 to 24.
J i . A transgenic plant or part thereof comprising a cell as claimed in claim 30.
32. A plasmid containing a DNA coding for expression of GRAB protein GRAB 1 or GRAB 2 described herein as deposited under the provisions of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms of 1977; these being
55
Figure imgf000007_0001
deposited on 1 1 June 1997 at the Coleccion Espanola de Cultivos Tipo, with the accession numbers CECT 4889 or CECT 4890 .
56
PCT/EP1998/003662 1997-06-12 1998-06-09 Plant grab proteins WO1998056811A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CA002289863A CA2289863A1 (en) 1997-06-12 1998-06-09 Plant grab proteins
AU82160/98A AU753798B2 (en) 1997-06-12 1998-06-09 Plant grab proteins
BR9809447-5A BR9809447A (en) 1997-06-12 1998-06-09 Plant grab proteins
NZ500529A NZ500529A (en) 1997-06-12 1998-06-09 Modifying GRAB1 and or GRAB2 (Geminivirus RepA Binding) to affect cell plant cycle using antisense sequences
EP98932162A EP0989997A2 (en) 1997-06-12 1998-06-09 Plant grab proteins
JP50164599A JP2002506345A (en) 1997-06-12 1998-06-09 Plant GRAB protein

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES009701292A ES2132025B1 (en) 1997-06-12 1997-06-12 URAG PROTEINS OF PLANTS.
ESP9701292 1997-06-12

Publications (4)

Publication Number Publication Date
WO1998056811A2 WO1998056811A2 (en) 1998-12-17
WO1998056811A3 WO1998056811A3 (en) 1999-03-04
WO1998056811B1 true WO1998056811B1 (en) 1999-04-08
WO1998056811A8 WO1998056811A8 (en) 2000-04-27

Family

ID=8299674

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1998/003662 WO1998056811A2 (en) 1997-06-12 1998-06-09 Plant grab proteins

Country Status (10)

Country Link
EP (1) EP0989997A2 (en)
JP (1) JP2002506345A (en)
CN (1) CN1260837A (en)
AU (1) AU753798B2 (en)
BR (1) BR9809447A (en)
CA (1) CA2289863A1 (en)
ES (1) ES2132025B1 (en)
NZ (1) NZ500529A (en)
WO (1) WO1998056811A2 (en)
ZA (1) ZA985135B (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6284947B1 (en) 1999-02-25 2001-09-04 Pioneer Hi-Bred International, Inc. Methods of using viral replicase polynucleotides and polypeptides
DE69919406T2 (en) * 1999-02-11 2005-09-08 Temasek Life Sciences Laboratory Ltd. NAC1- A PLANT ENGINE FOR A TRANSCRIPTION FACTOR INVOLVED IN THE DEVELOPMENT OF COTYLEDONES AND SIDE ROOTS
US6770800B2 (en) 1999-03-12 2004-08-03 Pioneer Hi-Bred International, Inc. Methods of using viral replicase polynucleotides and polypeptides
GB9923306D0 (en) 1999-10-01 1999-12-08 Isis Innovation Diagnostic and therapeutic epitope, and transgenic plant
FR2806095A1 (en) * 2000-03-10 2001-09-14 Gentech New polynucleotides for producing transgenic plants resistant to geminivirus infection comprising polynucleotides encoding proteins which interact with at least one of the products of the geminivirus genome
US20020188965A1 (en) * 2001-04-20 2002-12-12 Zou-Yu Zhao Methods of transforming plants
GB0212885D0 (en) 2002-06-05 2002-07-17 Isis Innovation Therapeutic epitopes and uses thereof
US10105437B2 (en) 2004-04-28 2018-10-23 Btg International Limited Epitopes related to coeliac disease
NZ550600A (en) 2004-04-28 2010-03-26 Btg Int Ltd Epitopes related to coeliac disease
JP4734959B2 (en) * 2005-02-25 2011-07-27 味の素株式会社 A novel plasmid capable of autonomous replication in microorganisms belonging to the family Enterobacteriaceae
CN106086005A (en) * 2016-08-22 2016-11-09 宁夏农林科学院 A kind of Wheat DNA rapid extracting method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2257972A1 (en) * 1996-06-13 1997-12-18 Consejo Superior De Investigaciones Cientificas Plant proteins

Also Published As

Publication number Publication date
ES2132025A1 (en) 1999-08-01
AU8216098A (en) 1998-12-30
ES2132025B1 (en) 2000-12-01
JP2002506345A (en) 2002-02-26
WO1998056811A3 (en) 1999-03-04
CA2289863A1 (en) 1998-12-17
NZ500529A (en) 2001-10-26
ZA985135B (en) 1999-12-13
CN1260837A (en) 2000-07-19
WO1998056811A2 (en) 1998-12-17
AU753798B2 (en) 2002-10-31
WO1998056811A8 (en) 2000-04-27
EP0989997A2 (en) 2000-04-05
BR9809447A (en) 2000-06-20

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