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WO2002002616A1 - Nouveau polypeptide, gamma-cop13, et polynucleotide codant ce polypeptide - Google Patents

Nouveau polypeptide, gamma-cop13, et polynucleotide codant ce polypeptide Download PDF

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Publication number
WO2002002616A1
WO2002002616A1 PCT/CN2001/000961 CN0100961W WO0202616A1 WO 2002002616 A1 WO2002002616 A1 WO 2002002616A1 CN 0100961 W CN0100961 W CN 0100961W WO 0202616 A1 WO0202616 A1 WO 0202616A1
Authority
WO
WIPO (PCT)
Prior art keywords
polypeptide
polynucleotide
gamma
sequence
seq
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/CN2001/000961
Other languages
English (en)
Chinese (zh)
Inventor
Yumin Mao
Yi Xie
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai Biowindow Gene Development Inc
Original Assignee
Shanghai Biowindow Gene Development Inc
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 Shanghai Biowindow Gene Development Inc filed Critical Shanghai Biowindow Gene Development Inc
Priority to AU10317/02A priority Critical patent/AU1031702A/en
Publication of WO2002002616A1 publication Critical patent/WO2002002616A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals

Definitions

  • a fragment, derivative or analog of the polypeptide of the present invention may be: (I) a kind in which one or more amino acid residues are replaced with conservative or non-conservative amino acid residues (preferably conservative amino acid residues), and the substitution
  • the amino acid may or may not be encoded by the genetic code; or (II) such a type in which a group on one or more amino acid residues is substituted by other groups to include a substituent; or (III) such A type in which a mature polypeptide is fused to another compound (such as a compound that extends the half-life of a polypeptide, such as polyethylene glycol); or (IV) a type of polypeptide sequence in which an additional amino acid sequence is fused into a mature polypeptide (such as the leader sequence or secreted sequence or the sequence used to purify this polypeptide or protease sequence)
  • such fragments, derivatives and analogs are considered to be within the knowledge of those skilled in the art.
  • polynucleotide encoding a polypeptide refers to a polynucleotide that includes the polypeptide and a polynucleotide that includes additional coding and / or non-coding sequences.
  • "strict conditions” means: (1) hybridization and elution at lower ionic strength and higher temperature, such as 0.2xSSC, 0.1% SDS, 6 (TC; or (2) Add a denaturant during hybridization, such as 50% (v / v) formamide, 0.1% calf serum / 0.1% Fi co ll, 42 ° C, etc .; or (3) only between two sequences Hybridization occurs only when the identity is at least 95%, and more preferably 97%.
  • the polypeptide encoded by the hybridizable polynucleotide has the same biological function and activity as the mature polypeptide shown in SEQ ID NO: 2 .
  • Methods known to those skilled in the art can be used to construct expression vectors containing a DNA sequence encoding gamnia-COP13 and appropriate transcriptional / translational regulatory elements. These methods include in vitro recombinant DNA technology, DNA synthesis technology, and in vivo recombination technology (Sambroook, et al. Molecular Cloning, a Laboratory Manual, cold Spring Harbor Laboratory. New York, 1989).
  • the DNA sequence (J) can be efficiently linked to an appropriate promoter in an expression vector to guide mRNA synthesis. Representative examples of these promoters are: the lac or trp promoter of E.
  • a peptide synthesizer (product of PE company) was used to synthesize the following peptides specific to a-C0P13:
  • polynucleotides of the present invention can be used as probes to be fixed on a microarray or a DM chip (also called a "gene chip") for analyzing differential expression analysis and gene diagnosis of genes in tissues.
  • a microarray or a DM chip also called a "gene chip”
  • Gamma-C0P13 specific primers for RNA-polymerase chain reaction (RT-PCR) in vitro amplification can also detect the transcript of ga-a-C0P13.
  • PCR localization of somatic hybrid cells is a quick way to localize DNA to specific chromosomes.
  • oligonucleotide primers of the present invention by a similar method, a set of fragments from a specific chromosome or a large number of genomic clones can be used to achieve sublocalization.
  • Other similar strategies that can be used for chromosomal localization include in situ hybridization, chromosome pre-screening with labeled flow sorting, and pre-selection of hybridization to construct chromosome-specific cDNA libraries.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Toxicology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

L'invention concerne un nouveau polypeptide, une gamma-COP13, et un polynucléotide codant ce polypeptide ainsi qu'un procédé d'obtention de ce polypeptide par des techniques recombinantes d'ADN. L'invention concerne en outre les applications de ce polypeptide dans le traitement de maladies, notamment des tumeurs malignes, de l'hémopathie, de l'infection par VIH, de maladies immunitaires et de diverses inflammations. L'invention concerne aussi l'antagoniste agissant contre le polypeptide et son action thérapeutique ainsi que les applications de ce polynucléotide codant la gamma-COP13.
PCT/CN2001/000961 2000-06-14 2001-06-11 Nouveau polypeptide, gamma-cop13, et polynucleotide codant ce polypeptide Ceased WO2002002616A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU10317/02A AU1031702A (en) 2000-06-14 2001-06-11 A novel polypeptide-gamma-cop13 and a polynucleotide encoding thesame

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN00116482.1 2000-06-14
CN 00116482 CN1328004A (zh) 2000-06-14 2000-06-14 一种新的多肽——gamma-COP13和编码这种多肽的多核苷酸

Publications (1)

Publication Number Publication Date
WO2002002616A1 true WO2002002616A1 (fr) 2002-01-10

Family

ID=4585886

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2001/000961 Ceased WO2002002616A1 (fr) 2000-06-14 2001-06-11 Nouveau polypeptide, gamma-cop13, et polynucleotide codant ce polypeptide

Country Status (3)

Country Link
CN (1) CN1328004A (fr)
AU (1) AU1031702A (fr)
WO (1) WO2002002616A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6121942B2 (ja) * 2014-05-15 2017-04-26 トヨタ自動車株式会社 植物のバイオマス量を増産させる遺伝子及びその利用方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
FEBS LETT., vol. 314, no. 2, 1992, pages 195 - 198 *
HUM. MOL. GENET., vol. 8, no. 13, 1999, pages 2387 - 2396 *

Also Published As

Publication number Publication date
CN1328004A (zh) 2001-12-26
AU1031702A (en) 2002-01-14

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