Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of... – Method of regulating cell metabolism or physiology
Reexamination Certificate
2000-07-18
2004-03-30
Lacourciere, Karen (Department: 1635)
Chemistry: molecular biology and microbiology
Animal cell, per se ; composition thereof; process of...
Method of regulating cell metabolism or physiology
C435S006120, C435S091100, C435S325000, C435S366000, C536S023100, C536S024310, C536S024330, C536S024500
Reexamination Certificate
active
06713302
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates generally to growth factors and specifically to a new member of the transforming growth factor beta (TGF-&bgr;) superfamily, which is denoted, growth differentiation factor6 (GDF-6).
2. Description of Related Art
The transforming growth factor P (TGF-P) superfamily encompasses a group of structurally-related proteins which affect a wide range of differentiation processes during embryonic development. The family includes, Mullerian inhibiting substance (MIS), which is required for normal male sex development (Behringer, et al.,
Nature
, 345:167, 1990), Drosophila decapentaplegic (DPP) gene product, which is required for dorsal-ventral axis formation and morphogenesis of the imaginal disks (Padgett, et al.,
Nature
, 325:81-84, 1987), the Xenopus Vg-1 gene product, which localizes to the vegetal pole of eggs ((Weeks, et al., Cell, 51: 861-867, 1987), the activins (Mason, et al.,
Biochem. Biophys. Res. Commun
., 135:957-964, 1986), which can induce the formation of mesoderm and anterior structures in Xenopus embryos (Thomsen, et al.,
Cell
, 63:485, 1990), and the bone morphogenetic proteins (BMPs, osteogenin, OP-1) which can induce de novo cartilage and bone formation (Sampath, et al.,
J. Biol. Chem
., 265:13198, 1990). The TGF-&bgr;s can influence a variety of differentiation processes, including adipogenesis, mycogenesis, chondrogenesis, hematopoiesis, and epithelial cell differentiation (for review, see Massague,
Cell
, 49:437, 1987).
The proteins of the TGF-&bgr; family are initially synthesized as a large precursor protein which subsequently undergoes proteolytic cleavage at a cluster of basic residues approximately 100-140 amino acids from the C-terminus. The C-terminal regions, or mature regions, of the proteins are all structurally related and the different family members can be classified into distinct subgroups based on the extent of their homology. Although the homologies within particular subgroups range from 70% to 90% amino acid sequence identity, the homologies between subgroups are significantly lower, generally ranging from only 20% to 50%. In each case, the active species appears to be a disulfide-linked dimer of C-terminal fragments. Studies have shown that when the pro-region of a member of the TGF-&bgr; family is coexpressed with a mature region of another member of the TGF-&bgr; family, intracellular dimerization and secretion of biologically active homodimers occur (Gray, A., and Matson, A.,
Science
, 247:1328, 1990). Additional studies by Hammonds, et al., (
Molec. Endocdn
. 5:149, 1991) showed that the use of the BMP-2 pro-region combined with the BMP4 mature region led to dramatically improved expression of mature BMP4. For most of the family members that have been studies, the homodimeric species has been found to be biologically active, but for other family members, like the inhibins (Ling, et al.,
Nature
, 321:779, 1986) and the TGF-&bgr;s (Cheifetz, et al.,
Cell
, 48:409, 1987), heterodimers have also been detected, and these appear to have different biological properties than the respective homodimers.
Identification of new factors that are tissue-specific in their expression pattern will provide a greater understanding of that tissue's development and function.
SUMMARY OF THE INVENTION
The present invention provides a cell growth and differentiation factor, GDF-6, a polynucleotide sequence which encodes the factor, and antibodies which are immunoreactive with the factor. This factor appears to relate to various cell proliferative disorders, especially those involving placental tissue.
Thus, in one embodiment, the invention provides a method for detecting a cell proliferative disorder of placental origin and which is associated with GDF-6. In another embodiment, the invention provides a method for treating a cell proliferative disorder by suppressing or enhancing GDF-6 activity.
REFERENCES:
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Lee, Se-Jin, “Expression of Growth/Differentiation Factor 1 in the Nervous System Conservation of a Bicistronic Structure,”Proc. Natl. Acad. Sci. USA, vol. 88, May 1991, pp. 4250-4254.
Bowie et al.,Science, 247:1306-10.
Rudinger,Peptide Hormones, Parsons ed., University Park Press, Baltimore, pp. 1-7.
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Ngo et al., “The Protein Folding Problem and Tertiary Structure Prediction,” Merz et al., Birkhuaser, Boston, pp. 491-495.
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Callard et al.,The Cytokine FactsBook, Academic Press, London, pp. 31-2.
Huynh Thanh
Lee Se-Jin
Gray Cary Ware & Freidenrich LLP
Haile Lisa A.
Lacourciere Karen
Schmidt M
The Johns Hopkins University School of Medicine
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