Expression and promoter analysis of mouse mastrin gene

Biochemical and Biophysical Research Communications

Volumn 307, Issue 3, 2003, Pages 491-497

  Chang, Mau Sun ^a,b   Chen, Chiung Ya ^a   Huang, Chang Jen ^c   Fan, Chi Chen ^a   Chu, Jien Ming ^a   Yang, Yuh Cheng ^a,d  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL TAIPEI UNIVERSITY OF TECHNOLOGY   (Taiwan)

^c INSTITUTE OF BIOLOGICAL CHEMISTRY   (Taiwan)

^d TAIPEI MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Astrin; Genomic structure; Mastrin; Microtubule

Indexed keywords

ASTRIN; MASTRIN; MICROTUBULE ASSOCIATED PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA FLANKING REGION; ENZYME LINKED IMMUNOSORBENT ASSAY; EXON; GENE DELETION; GENE ISOLATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; IMMUNOFLUORESCENCE; MITOSIS; MITOSIS SPINDLE; MOLECULAR CLONING; MOUSE; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; TATA BOX;

EID: 0042171511     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-291X(03)01220-8     Document Type: Article

References (31)

1. Compton D.A. Spindle assembly in animal cells. Annu. Rev. Biochem. 69:2000;95-114.
2. Wittmann T., Hyman A., Desai A. The spindle: a dynamic assembly of microtubules and motors. Nature Cell Biol. 3:2001;E28-E34.
3. Karsenti E., Vernos I. The mitotic spindle: a self-made machine. Science. 294:2001;543-547.
4. Heald R. Motor function in the mitotic spindle. Cell. 102:2000;399-402.
5. Sharp D.J., Rogers G.C., Scholey J.M. Microtubule motors in mitosis. Nature. 407:2000;41-47.
6. Andersen S.S., Buendia B., Dominguez J.E., Sawyer A., Karsenti E. Effect on microtubule dynamics of XMAP230, a microtubule-associated protein present in Xenopus laevis eggs and dividing cells. J. Cell Biol. 27:1994;1289-1299.
7. Andersen S.S., Karsenti E. XMAP310, a Xenopus rescue-promoting factor localized to the mitotic spindle. J. Cell Biol. 139:1997;975-983.
8. Charrasse S.M., Schroeder M., Gauthier-Rouviere C., Ango F., Cassimeris L., Gard D.L., Larroque C. The TOGp protein is a new human microtubule-associated protein homologous to the Xenopus XMAP215. J. Cell Biol. 111:1998;1371-1383.
9. Belmont L., Mitchison T.J. Identification of a protein that interacts with tubulin dimers and increases the catastrophe rate of microtubules. Cell. 84:1996;623-631.
10. McNally F.J., Okawa K., Iwamatsu A., Valve R.D. Katanin, the microtubule-severing ATPase, is concentrated at centrosomes. J. Cell Sci. 109:1996;561-567.
11. Compton D.A., Cleveland D.W. NuMA, a nuclear protein involved in mitosis and nuclear reformation. Curr. Opin. Cell Biol. 6:1994;343-346.
12. Wittmann T., Wilm M., Karsenti E., Vernos I. TPX2, A novel Xenopus MAP involved in spindle pole organization. J. Cell Biol. 149:2000;1405-1418.
13. Gergely F., Karlsson C., Still I., Cowell J., Kilmartin J., Raff J.W. The TACC domain identifies a family of centrosomal proteins that can interact with microtubules. Proc. Natl. Acad. Sci. USA. 97:2000;14352-14357.
14. Inoue Y.H., do armo Avides M., Shiraki M., Deak P., Yamaguchi M., Nishimoto Y., Matsukage A., Glover D.M. Orbit, a novel microtubule-associated protein essential for mitosis in Drosophila melanogaster. J. Cell Biol. 149:2000;153-166.
15. Mack G.J., Compton D.A. Analysis of mitotic microtubule-associated proteins using mass spectrometry identifies astrin, a spindle-associated protein. Proc. Natl. Acad. USA. 97:2001;14352-14357.
16. Gruber J., Harborth J., Schnabel J., Weber K., Hatzfeld M. The mitotic-spindle associated protein astrin is essential for progression through mitosis. J. Cell Sci. 115:2002;4053-4059.
17. Chang M.-S., Huang C.-J., Chen, M.-L., Chen S.-T., Fan C.-C., Chu, J.-M., Lin W.-C., Yang Y.-C. Cloning and characterization of hMAP126, a new member of mitotic spindle-associated proteins. Biochem. Biophys. Res. Commun. 287:2001;116-121.
18. Smale S.T. Transcription initiation from TATA-less promoters within eukaryotic protein-coding genes. Biochim. Biophy. Acta. 1351:1997;73-88.
19. Shao X., Xue J., van der Hoorn F.A. Testicular protein Spag5 has similarity to mitotic spindle protein Deepest and binds outer dense fiber protein Odf1. Mol. Reprod. Dev. 59:2001;410-416.
20. Xue J., Shao X., Rancourt D.E., van der Hoorn F.A. Targeted disruption of the Testicular Spag5/Deepest protein does not affect spermatogenesis or fertility. Mol. Cell. Biol. 22:2002;1993-1997.
21. Zwicker J., Gross C., Lucibello F.C., Truss M., Ehlert F., Engeland K., Muller R. Cell cycle regulation of cdc25C transcription is mediated by the periodic repression of the glutamine-rich activators NF-Y and Sp1. Nucleic Acids Res. 23:1995;3822-3830.
22. Zwicker J., Lucibello F.C., Wolfraim L.A., Gross C., Truss M., Engeland K., Muller R. Cell cycle regulation of the cyclin A, cdc25C and cdc2 genes is based on a common mechanism of transcriptional repression. EMBO J. 14:1995;4514-4522.
23. Shimizu M., Ichikawa E., Inoue U., Nakamura T., Nakajima T., Nojima H., Okayama H., Oda K. The G1/S boundary-specific enhancer of the rat cdc2 promoter. Mol. Cell. Biol. 15:1995;2882-2892.
24. Huet X., Rech J., Plet A., Vie A., Blanchard J.M. Cyclin A expression is under negative transcriptional control during the cell cycle. Mol. Cell. Biol. 16:1996;3789-3798.
25. Katula K.S., Wright K.L., Paul H., Surman D.R., Nuckolls F.J., Smith J.W., Ting J.P., Yates J., Cogswell J.P. Cyclin-dependent kinase activation and S-phase induction of the cyclin B1 gene are linked through the CCAAT elements. Cell Growth Differ. 8:1997;811-820.
26. Farina A., Manni I., Fontemaggi G., Tiainen M., Cenciarelli C., Bellorini M., Mantovani R., Sacchi A., Piaggio G. Down-regulation of cyclin B1 gene transcription in terminally differentiated skeletal muscle cells is associated with loss of functional CCAAT-binding NF-Y complex. Oncogene. 18:1999;2818-2827.
27. Suske G. The Sp-family of transcription factors. Gene. 238:1999;291-300.
28. Mantovani R. A survey of 178 NF-Y binding CCAAT boxes. Nucleic Acid Res. 26:1998;1135-1143.
29. Rice P.A. Making DNA do a U-turn: IHF and related proteins. Curr. Opin. Struct. Biol. 7:1997;86-93.
30. Trojanowska M. Ets factors and regulation of the extracellular matrix. Oncogene. 19:2000;6464-6471.
31. Merika M., Orkin S.H. DNA-binding specificity of GATA family transcription factors. Mol. Cell. Biol. 13:1993;3999-4010.