EP1230359A1 - Homologues de type chordine - Google Patents
Homologues de type chordineInfo
- Publication number
- EP1230359A1 EP1230359A1 EP00973208A EP00973208A EP1230359A1 EP 1230359 A1 EP1230359 A1 EP 1230359A1 EP 00973208 A EP00973208 A EP 00973208A EP 00973208 A EP00973208 A EP 00973208A EP 1230359 A1 EP1230359 A1 EP 1230359A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- clh
- nucleic acid
- acid sequence
- sequence
- product
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- SEQ ID NO: 1 The sequence shown in SEQ ID NO: 1 is a homolog to the known chordins within the VWFC domain, named after the von-Willebrand factor (VWF) type C repeat, which is found 2-4 times in these multi-domain proteins.
- VWF domain has a length of about 70 amino acids covering 10 well conserved cysteines.
- the present invention provides a nucleic acid molecule comprising or consisting of a non-coding sequence which is complementary to that of any one of SEQ ID NO: 1 to SEQ ID NO: 11, or complementary to a sequence having at least 70%, preferably 80%), most preferably 90% or 95% identity to said sequence or a fragment of said two sequences.
- the complementary sequence may be a DNA sequence which hybridizes with any one of the sequences of SEQ ID NO: 1 to SEQ ID NO: 11, or hybridizes to a portion of that sequence having a length sufficient to inhibit the transcription of the complementary sequence.
- compositions of the invention may be used also for the treatment of osteoporosis pseudoglioma syndrome, autosomal recessive osteopetrosis, and isolated increased bone mass (high bone mass without other clinical features).
- the CLH of the invention may also be used for augmenting bone regeneration after injury, so as to speed up the healing process.
- Alexander Disease This disorder, is characterized clinically by development of megalencephaly in infancy accompanied by progressive spasticity and dementia. In this disorder astrocytes show marked changes.
- the amount of the antibody-antigen complex can be quantitized, in order to determine the level of the CHL-product or the anti-CHL antibodies, as the case may be.
- Fig. 4a is the alignment of the third splice variant (SEQ ID NO: 15) with a known chordin deposited in the Emb under gi 4808227;
- Fig. 13 shows the alignment of SEQ ID No. 19 to the known chordin deposited as gi 2731578;
- Fig. 14 shows the alignment of SEQ ID No. 18 to the known chordin deposited as gi 3822218;
- Fig. 15 shows the alignment of SEQ ID No. 20 to the known chordin deposited as gi 2731578;
- Fig. 16 shows the alignment of SEQ ID No. 20 to the known chordin deposited as gi 382218;
- Fig. 22 shows a Northern blot analysis of CLH expression in: skeletal muscles, uterus, colon, small intestine, bladder, heart, stomach, prostate;
- the expression vectors preferably contain one or more selectable marker genes to provide a phenotypic trait for selection of transformed host cells such as dihydrofolate reductase or neomycin resistance for eukaryotic cell culture, or such as tetracycline or ampicillin resistance in E.coli.
- the vector containing the appropriate DNA sequence as described above, as well as an appropriate promoter or control sequence, may be employed to transform an appropriate host to permit the host to express the protein.
- the expression of a sequence encoding CLH product may be driven by any of a number of promoters.
- viral promoters such as the 35S and 19S promoters of CaMV (Brisson et al, Nature 310:511-514. (1984)) may be used alone or in combination with the omega leader sequence from TMV (Takamatsu et al, EMBO J., 3:17-311, (1987)).
- plant promoters such as the small subunit of RUBISCO (Coruzzi et al., EMBO J.
- CLH product may also be expressed in an insect system.
- Autographa cahfornica nuclear polyhedrosis virus (AcNPV) is used as a vector to express foreign genes in Spodoptera frugiperda cells or in Trichoplusia larvae.
- the CLH product coding sequence may be cloned into a nonessential region of the vims, such as the polyhedrin gene, and placed under control of the polyhedrin promoter. Successful insertion of CLH coding sequence will render the polyhedrin gene inactive and produce recombinant virus lacking coat protein coat.
- the recombinant viruses are then used to infect S. frugiperda cells or Trichoplusia larvae in which CLH protein is expressed (Smith et al, J.
- the probe is a nucleic acid molecule of at least 20 nucleotides, preferably 20-30 nucleotides, capable of specifically hybridizing with a sequence included within the sequence of a nucleic acid molecule encoding CLH under hybridizing conditions, detecting the presence of mRNA hybridized to the probe, and thereby detecting the expression of CLH.
- This assay can be used to distinguish between absence, presence, and excess expression of CLH product and to monitor levels of CLH expression during therapeutic intervention.
- the substantially purified CLH product of the invention has been defined above as the product coded from the nucleic acid sequence of the invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL13284699 | 1999-11-10 | ||
IL13284699A IL132846A0 (en) | 1999-11-10 | 1999-11-10 | Novel nucleic acid and amino acid sequences |
IL13376799A IL133767A0 (en) | 1999-12-28 | 1999-12-28 | Novel nucleic acid and amino acid sequences |
IL13376799 | 1999-12-28 | ||
PCT/IL2000/000736 WO2001034796A1 (fr) | 1999-11-10 | 2000-11-10 | Homologues de type chordine |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1230359A1 true EP1230359A1 (fr) | 2002-08-14 |
Family
ID=26323900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00973208A Withdrawn EP1230359A1 (fr) | 1999-11-10 | 2000-11-10 | Homologues de type chordine |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1230359A1 (fr) |
AU (1) | AU1174501A (fr) |
WO (1) | WO2001034796A1 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003525611A (ja) * | 2000-03-02 | 2003-09-02 | アムジェン インコーポレーテッド | コルディン様−2分子およびその使用 |
AU2001249608A1 (en) * | 2000-03-28 | 2001-10-08 | Beth Israel Deaconess Medical Center | Bladder cancer-specific peptides for diagnosis and therapy |
WO2005014817A2 (fr) * | 2003-08-07 | 2005-02-17 | Compugen Ltd. | Homologues de type chordine |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU6552198A (en) * | 1997-03-14 | 1998-09-29 | Human Genome Sciences, Inc. | 28 human secreted proteins |
WO2000012708A2 (fr) * | 1998-09-01 | 2000-03-09 | Genentech, Inc. | Nouveaux pro-polypeptides et sequences correspondantes |
DE19817946A1 (de) * | 1998-04-17 | 1999-10-21 | Metagen Gesellschaft Fuer Genomforschung Mbh | Menschliche Nukleinsäuresequenzen aus Uterus-Normalgewebe |
JP2003525575A (ja) * | 1998-05-07 | 2003-09-02 | ジェネティックス・インスチチュート・リミテッド・ライアビリティ・カンパニー | 分泌蛋白およびそれらをコードするポリヌクレオチド |
AU5475199A (en) * | 1998-08-10 | 2000-03-06 | Genetics Institute Inc. | Human chordin-related proteins and polynucleotides encoding them |
EP1179066A2 (fr) * | 1999-05-19 | 2002-02-13 | Incyte Genomics, Inc. | Molecules de signalisation extracellulaires |
-
2000
- 2000-11-10 WO PCT/IL2000/000736 patent/WO2001034796A1/fr not_active Application Discontinuation
- 2000-11-10 EP EP00973208A patent/EP1230359A1/fr not_active Withdrawn
- 2000-11-10 AU AU11745/01A patent/AU1174501A/en not_active Abandoned
Non-Patent Citations (1)
Title |
---|
See references of WO0134796A1 * |
Also Published As
Publication number | Publication date |
---|---|
AU1174501A (en) | 2001-06-06 |
WO2001034796A1 (fr) | 2001-05-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20020610 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: BITON, SHARON Inventor name: BERNSTEIN, JEANNE Inventor name: SAVITZKY, KINNERET Inventor name: TOPOROIK, AMIR |
|
17Q | First examination report despatched |
Effective date: 20050608 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20051220 |