Cell Cycle-Associated Autoantibodies: Markers for Autoimmunity and Probes for Molecular Cell Biology

References

• Tan E. M. Antinuclear antibodies: Diagnostic markers for autoimmune diseases and probes for cell biology. Adv. Immunol. 1989; 44: 93–151
   PubMed Web of Science ®Google Scholar
• Campbell P., McCluskey J., Yeo IP, Toh B. H. Electroporation of antibodies into mammalian cells. Electroporation and Electrofusion Protocols, J A. Nick-Oloff. Humana Press. 1994
   Google Scholar
• Norbury C., Nurse P. Animal cell cycles and their control. Ann. Rev. Biochem. 1992; 61: 441–470
   PubMed Web of Science ®Google Scholar
• Scherr C. J. Mammalian Gl cyclins. Cell 1993; 73: 1059–1065
   Google Scholar
• Nigg E. A. Targets of cyclin-dependent protein kinases. Curr. Opin. Cell Biol. 1993; 5: 187–193
   PubMed Web of Science ®Google Scholar
• Cohen P. The structure and regulation of protein phosphatases. Ann. Rev. Biochem. 1989; 58: 453–508
   PubMed Web of Science ®Google Scholar
• Hubbard M J., Cohen P. On target with a new mechanism for the regulation of protein phosphorylation. TIBS 1993; 18: 172–177
   PubMed Web of Science ®Google Scholar
• Wadsworth P. Mitosis: spindle assembly and chromosome motion. Curr. Opin. Cell Biol. 1993; 5: 123–128
   Google Scholar
• Karsenti E., Maro B. Centrosomcs and the spatial distribution of microtubules in animal cells. TIBS 1986; 11: 460–463
   Web of Science ®Google Scholar
• Kalt A., Schliwa M. Molecular components of the centrosome. Trends in Cell Biol. 1993; 3: 118–128
   PubMedGoogle Scholar
• Prelich G., Tan C-K., Kostura M., Mathews M B., So A H., Downey K M., Stillman B. Functional identity of proliferating cell nuclear antigen and a DNA polymerase 5 auxiliary protein. Nature 1987b; 326: 517–520
   PubMed Web of Science ®Google Scholar
• Bravo R., Frank R., Blundell P A., Macdonald-Bravo H. Cyclin/PCNA is the auxiliary protein of DNA polymerase 8. Nature 1987; 326: 515–517
   PubMed Web of Science ®Google Scholar
• Prelich G., Kostura M., Marshak D R., Mathews M B., Stillman B. The cell-cycle regulated proliferating cell nuclear antigen is required for SV40 DNA replication in vitro. Nature 1987a; 326: 471–475
   PubMed Web of Science ®Google Scholar
• Jaskulski D., DeReil J K., Mercer W E., Calabretta B., Baserga R. Inhibition of cellular proliferation by antisense oligodeoxynucleotides to PCNA cyclin. Science 1988; 240: 1544–1546
   PubMed Web of Science ®Google Scholar
• Zuber M., Tan E M., Ryoji M. Involvement of proliferating cell nuclear antigen (cyclin) in DNA replication in living cells. Mol. Cell. Biol. 1989; 9: 57–66
   PubMedGoogle Scholar
• Shiviji M K.K., Kenny M K., Wood R D. Proliferating cell nuclear antigen is required for DNA excision repair. Cell 1992; 69: 367–374
   Google Scholar
• Tuffanelli D., McKeon F., Kleinsmith D M., Burnham T K., Kirschner M. Anti-centrosome and anti-centriole antibodies in the scleroderma spectrum. Arch. Dermatol. 1983; 119: 560–566
   PubMed Web of Science ®Google Scholar
• Calarco-Gillam P D., Siebert M C., Hubble R., Mitchison T., Kirschner M. Centrosome development in early mouse embroys as defined by an autoantibody against peri-centriolar material. Cell 1983; 35: 621–629
   PubMed Web of Science ®Google Scholar
• Clayton L., Black CM., Lloyd C W. Microtubule nucleating sites in higher plant cells identified by an autoantibody against pericentriolar material. J. Cell Biol. 1985; 101: 319–324
   PubMed Web of Science ®Google Scholar
• Bastmeyer M., Steffen W., Fuge H. Immunostaining of spindle components in tipulid spermatocytes using a serum against pericentriolar material. Eur. J. Cell Biol. 1986; 42: 305–310
   PubMedGoogle Scholar
• Snyder M., Davis R W. SPA1: A gene important for chromosomal segregation and other mitotic functions in S. cerevisiae. Cell 1988; 54: 743–754
   PubMedGoogle Scholar
• Doxsey S J., Stein P., Evans L., Calarco P D., Kirschner M. Pericentrin, a highly conserved centrosome protein involved in microtubule organisation. Cell 1994; 76: 639–650
   PubMed Web of Science ®Google Scholar
• Oliver J M., Sager P R., Senecal J-L., Rothfield N L. A mitotic-specific autoantibody in human serum. J. Cell Biol. 1983; 97: 43a
   Google Scholar
• Senecal J-L., Oliver J M., Rothfield N. Anticytoskeletal autoantibodies in connective tissue diseases. Arthritis Rheum. 1985; 28: 889–994
   PubMed Web of Science ®Google Scholar
• Sager P R., Rothfield N L., Oliver J M., Berlin R D. A novel mitotic spindle pole component that originates from the cytoplasm during prophase. J. Cell Biol. 1986; 103: 1863–1872
   Google Scholar
• Rattner J B., Martin L., Waisman D M., Johnstone S A., Fritzler M J. Autoantibodies to the centrosome (centri-ole) react with determinants present in the glycolytic enzyme enolase. J. Immunol. 1991; 146: 2341–2344
   PubMed Web of Science ®Google Scholar
• Balczon R., West K. The identification of mammalian centrosomal antigens using human autoimmune anticen-trosome antisera. Cell Motility and the Cytoskeleton 1991; 20: 121–135
   Google Scholar
• Balczon R., Bao L., Zimmer W E. PCM-1, a 228 kDa centrosome autoantigen with a distinct cell cycle distribution. J. Cell Biol. 1994; 124: 783–793
   PubMedGoogle Scholar
• Yeo J P., Alderuccio F., Toh B H. A new chromosomal protein essential for mitotic spindle assembly. Nature 1994; 367: 288–291
   PubMed Web of Science ®Google Scholar
• Karsenti E. Mitotic spindle morphogenesis in animal cells. Sem. in Cell Biol. 1991; 2: 251–260
   PubMedGoogle Scholar
• Yeo J P., Forer A., Toh B H. A homologue of human regulator of mitotic spindle assembly protein (RMSA-1) is present in Crane fly and associated with meiotic chromosomes. J CellSci. 1994; 107: 1845–1851
   PubMed Web of Science ®Google Scholar
• Moir R D., Goldman R D. Lamin dynamics. Curr. Opin. Cell Biol. 1993; 5: 408–411
   Google Scholar
• McKeon F D., Tuffaneli D A., Fikuyama K., Kirschner M W. Autoimmune response directed against conserved determinants of nuclear envelope proteins in a patient with linear scleroderma. Proc. Natl. Scad. Sci. USA 1983; 80: 4374–4378
   PubMedGoogle Scholar
• Reeves W H., Chaudhary N., Salerno A., Blobel G., Lamin B. autoantibodies in sera from patients of certain patients with systemic lupus erythematosus. J. Exp. Med. 1987; 165: 750–762
   PubMedGoogle Scholar
• Guilly M-N., Danon F., Brouet J-C, Bornens M., Courvalin J-C. Autoantibodies to nuclear lamin B in a patient with thrombopenia. Eur. J. Cell Biol. 1987; 43: 266–272
   PubMedGoogle Scholar
• Lassoued S., Oksman E., Fournie B., Danon F., Fournie A., Lassoued K. Autoantibodies to lamins in rheumatoid arthritis. Arthritis Rheum. 1990; 33: 877–879
   Google Scholar
• Lassoued K., Guilly M-N., Danon F., Andre C, Dhumeaux D., Clavel J-P., Brouet J-C, Seligmann M., Courvalin J-C. Antinuclear autoantibodies specific for nuclear lamins: Characterisation and clinical significance. Ann. Intern. Med. 1988; 108: 829–833
   PubMedGoogle Scholar
• Konstantinov K., Halberg P., Wilk A., Hoier-Madsen M., Wantzin P., Ullman S., Galchcva-Gargova Z. Clinical manifestations of patients with autoantibodies specific for nuclear lamin proteins. Clin. Immunol. Immunopathol. 1992; 62: 112–118
   Google Scholar
• Wesierska-Gadck J., Penner E., Hitchman E., Sauer-Mann G. Antibodies to nuclear lamins in autoimmune liver diseases. Clin. Immunol. Immunopathol. 1988; 49: 107–115
   Google Scholar
• Wesierska-Gadek J., Penner E., Hitchman E., Sauer-Mann G. Antibodies to nuclear lamin C in chronic hepatitis delta virus infection. Hepathology 1990; 12: 1129–1133
   Google Scholar
• Chou C-H., Reeves W H. Recognition of multiple epitopes in the coiled-coil domain of lamin B by human autoantibodies. Mol. Immunol. 1992; 29: 1055–1064
   Google Scholar
• Mariette X., Brouet J-L., Danon F., Tsapis A., Las-Soued K. Nucleotide sequence analysis of the VI and Vh domains of five human IgM directed to lamin B. Arthritis Rheum. 1993; 36: 1315–1324
   PubMedGoogle Scholar
• Senecal J.-L., Raymond Y. Autoantibodies to major and minor nuclear lamins are not restricted to autoimmune diseases. Clin. Immunol. Immunopathol. 1982; 63: 115–125
   Google Scholar
• Moroi Y., Peebles M J., Fritzler M J., Tan E M. Autoantibody to centromere (kinetochores) in scleroderma sera. Proc. Natl. Acad. Sci. USA 1980; 77: 1627–1631
   PubMed Web of Science ®Google Scholar
• Tan E M., Rodana G P., Garcia I., Moroi Y., Fritzler M J., Peebles C. Diversity of antinuclear antibodies in progressive systemic sclerosis: anti-centromere antibody and its relationship to CREST syndrome. Arthritis Rheum. 1980; 23: 617–625
   PubMed Web of Science ®Google Scholar
• Kallenberg C G.M., Pastoor G W., Wouda A A., The T H. Antinuclear antibodies in patients with Raynaud's phenomenon: clinical significance of anticentromere antibodies. Ann. Rheum. Dis. 1982; 41: 382–387
   PubMed Web of Science ®Google Scholar
• Bernstein R M., Callender M E., Neuberger J M., Hughes C R.V., Williams R. Anticentromere antibody in primary biliary cirrhosis. Ann. Rheum. Dis. 1982; 41: 612–614
   PubMed Web of Science ®Google Scholar
• Lee S-L., Tsay G J., Tsai R-T. Anticentromere antibodies in subjects with no apparent connective tissue disease. Ann. Rheum. Dis. 1993; 52: 586–589
   PubMed Web of Science ®Google Scholar
• Palmer D K., O'Day K., Trong H L., Charbonneau H., Margolis R L. Purification of the centromere-specific protein CENT-A and demonstration that it is a distinctive histone. Proc. Natl. Acad. Sci. USA 1991; 88: 3734–3738
   PubMedGoogle Scholar
• Masumoto H., Masukata H., Muro Y., Nozaki N., Okazaki T. A human centromere antigen (CENT-B) interacts with a short specific sequence in alphoid DNA, a human centromeric satellite. J. Cell Biol. 1990; 109: 1963–1973
   Google Scholar
• Earnshaw W C., Sullivan K F., Machlin P S., Cooke C A., Kaiser D A., Pollard T D., Rothfield N F., Cleveland D W. Molecular cloning of cDNA for CENT-B, the major human centromere autoantigen. J. Cell Biol. 1987; 104: 817–829
   PubMed Web of Science ®Google Scholar
• Saitoh H., Tomkiel J., Cooke C. A., Ratrie H., Maurer M., Rothfield N F., Earnshaw W C. CENT-C, an autoantigen in scleroderma, is a component of the inner kinetochore plate. Cell 1992; 70: 115–125
   PubMedGoogle Scholar
• Bischoff F R., Maier G., Tilz G., Ponstingl H. A 47 kd human nuclear protein recognised by antikinetochore sera is homologous with the protein encoded by RCC1, a gene implicated in onset of chromosome condensation. Proc. Natl. Acad. Sci. USA 1990; 87: 8617–8621
   PubMedGoogle Scholar
• Simerly C, Balczon R., Brinklcy B R., Schatten G. Microinjected kinetochore antibodies interfere with chromosome movement in meiotic and mitotic mouse oocytes. J. Cell Biol. 1990; 111: 1491–1504
   PubMed Web of Science ®Google Scholar
• Bernat R L., Delannoy M R., Rothfield N F., Earnshaw W C. Disruption of centromere assembly during interphase inhibits kinetochore morphogenesis and function in mitosis. Cell 1991; 66: 1229–1238
   PubMedGoogle Scholar
• Wise D A., Lakshmisri B. Antikinetochore antibodies interfere with prometaphase but not anaphase chromosome movement in living PtK2 cells. Cell Motility and Cytoskel-eton 1992; 23: 157–167
   Google Scholar
• Nishimoto T., Eilen E., Basilico C. Premature chromosome condensation in a ts DNA-mutant of BHK cells. Cell 1978; 15: 475–483
   PubMedGoogle Scholar
• Bischoff F R., Ponstingl H. Mitotic regulator protein RCC1 is complexcd with a nuclear ras-related polypeptide. Proc. Natl. Acad. Sci. USA 1991; 88: 10830–10834
   PubMed Web of Science ®Google Scholar
• Bischoff F R., Ponstingl H. Catalysis of guanine nucleotide exchange on Ran by the mitotic regulator RCC1. Nature 1991; 354: 80–82
   PubMed Web of Science ®Google Scholar
• Dasso M. RCC1 in the cell cycle: the regulator of chromosome condensation takes on new roles. TIBS 1993; 18: 96–101
   PubMed Web of Science ®Google Scholar
• Guldner H H., Lakomek H J., Bautz F B. Human anti-centromere sera recognize a 19.5 non-histone chromosomal protein from HeLa cells. Clin. Exp. Immunol. 1984; 58: 13–20
   PubMedGoogle Scholar
• Earnshaw W L., Rothfield N. Identification of a family of human centromere proteins using autoimmune sera from patients with scleroderma. Chromosoma 1985; 91: 313–321
   PubMed Web of Science ®Google Scholar
• Saunders W S., Chue C, Goebl M., Craig C, Clark R F., Powers J A., Eissenberg J C., Elgin S C., Rothfield N F., Earnshaw W C. Molecular cloning of a human homo-logue of Drosophila hcterochromatin protein HP1 using anti-centromere autoantibodies with anti-chromo specificity. J. Cell Sci. 1993; 104: 573–583
   PubMed Web of Science ®Google Scholar
• Lynderson B., Pettijohn D. Human-specific nuclear protein that associates with the polar region of the mitotic apparatus: distribution in a human/hamster hybrid cell. Cell 1980; 22: 489–499
   Google Scholar
• McCarty G A., Valencia D W., Fritzler M J. Antibody to the mitotic spindle: immunologic characteristics and cytologic studies. J. Rheumatology 1984; 11: 213–218
   PubMedGoogle Scholar
• Yang C H., Lambie E J., Snyder M. NuMA: An unsu-ally long coiled-coiled related protein in the mammalian nucleus. J. Cell Biol. 1992; 116: 1303–1317
   PubMedGoogle Scholar
• Compton D A., Szilak I., Cleveland D W. Primary structure of NuMA, an intranuclear protein that defines a novel pathway for segregation of proteins at mitosis. J. Cell Biol. 1992; 116: 1395–1408
   PubMed Web of Science ®Google Scholar
• Tousson A., Zeng B., Brinkley B R., Valdivia K. Centro-philin: a novel mitotic spindle protein involved in microtubule nucleation. J. Cell Biol. 1991; 112: 427–440
   Google Scholar
• Maekawa T., Leslie R., Kuriyama R. Identification of a minus-end-specific microtubule-associated protein located at the mitotic poles in cultured mammalian cells. Eur. J. Cell Biol. 1991; 54: 255–267
   Google Scholar
• Kallajoki M., Weber K., Osborn M. A 210 kD nuclear matrix protein is a functional part of the mitotic spindle: a microinjection study using SPN monoclonal antibodies. EMBOJ. 1991; 10: 3351–3362
   PubMedGoogle Scholar
• Lind K., Hoier-Madsen M., Wilk A. Autoantibodies to the mitotic spindle apparatus in Mycoplasma pneumoniae disease. Infection and Immunity 1988; 56: 714–715
   Google Scholar
• Buck R C., Tisdale J M. The fine structure of the midbody of the rat erythrocyte. J. Cell Biol. 1962; 13: 109–115
   PubMedGoogle Scholar
• Kingwell B., Fritzler M., Decoteau J., Rattner J B. Identification and characterisation of a protein associated with the stembody using autoimmune sera from patients with systemic sclerosis. Cell Mold. Cytoskeleton 1987; 8: 360–367
   Google Scholar
• Cooke C A., Heck M M.S., Earnshaw W C. The IN-CENP antigens: movement from the inner centromere to the midbody during mitosis. J. Cell Biol. 1987; 105: 2053–2067
   PubMed Web of Science ®Google Scholar
• Yen T J., Li G., Schaar B T., Szilak I., Cleveland D W. CENT-E is a putative kinetochore motor that accumulates just before mitosis. Nature 1992; 359: 536–539
   PubMed Web of Science ®Google Scholar
• Nislow C, Lombillo V A., Kuriyama R., McIntosh J R. A plus-end directed motor enzyme that moves antipar-allel microtubules in vitro localises to the interzone of mitotic spindles. Nature 1992; 359: 543–547
   PubMed Web of Science ®Google Scholar
• Rattner J B., Wang T., Mack M., Martin L., Fritzler M J. MSA-35: a protein identified by human autoantibodies that colocalises with microtubules. Biochem. Cell Biol. 1992; 70: 1115–1122
   Google Scholar
• Rattner J B., Wang T., Mack M., Fritzler M J., Martin L., Valencia D. MSA-36: A chromosomal and mitotic spindle-associated protein. Chromosoma 1992; 101: 625–633
   Google Scholar
• Earnshaw W C., Bernat R L. Chromosomal passengers: Toward an integregated view of mitosis. Chromosoma 1991; 100: 139–146
   PubMedGoogle Scholar
• Gordon T., Topfer F., Keech C, Reynolds P., Chen W., Rischmueller M., McCluskey J. How does autoimmunity to La and Ro initiate and spread?. Autoimmunity 1994
   Google Scholar
• Toh B H. Anti-cytoskeletal autoantibodies: diagnosis significance for liver diseases, infections and systemic autoimmune diseases. Autoimmunity 1991; 11: 119–125
   PubMed Web of Science ®Google Scholar