Back to Search
Start Over
A cell-cycle nuclear autoantigen containing WD-40 motifs expressed mainly in S and G2 phase cells.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1995 Feb 27; Vol. 207 (3), pp. 1029-37. - Publication Year :
- 1995
-
Abstract
- Recently a novel nuclear protein mainly expressed in S and G2 phase cells was characterized using autoantibodies from a cancer patient (Exp. Cell Res., 212, 255-261, 1994). cDNA clones were isolated by immunoscreening, and sequence analysis revealed that the cDNA clones encoded a 713-amino acid residue polypeptide which is provisionally named SG2NA (S/G2 nuclear antigen). In the carboxyl terminal half of SG2NA, there are 6 copies of WD-40 motifs characteristic of a large family of proteins of which the prototype is beta-transducin/enhancer of split (TLE). In addition, there are nuclear localization sequence and phosphorylation sites related to the TLE proteins. Autoantibodies occurring spontaneously in certain cancer patients have been useful reagents for identifying cellular proteins and this is the first report of a novel WD-40 protein which is the target of an autoimmune response.
- Subjects :
- Adenocarcinoma immunology
Adenocarcinoma secondary
Amino Acid Sequence
Autoantibodies
Autoimmunity
Base Sequence
Cloning, Molecular
DNA, Complementary chemistry
DNA, Complementary genetics
Humans
Lung Neoplasms immunology
Lung Neoplasms secondary
Molecular Sequence Data
Nuclear Proteins chemistry
Proliferating Cell Nuclear Antigen chemistry
Proliferating Cell Nuclear Antigen genetics
Urinary Bladder Neoplasms immunology
Autoantigens analysis
G2 Phase immunology
Nuclear Proteins immunology
Proliferating Cell Nuclear Antigen analysis
S Phase immunology
Transducin chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 207
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 7864889
- Full Text :
- https://doi.org/10.1006/bbrc.1995.1288