Mapping of human non-muscle type cofilin (CFL1) to chromosome 11q13 and muscle-type cofilin (CFL2) to chromosome 14

Annals of Human Genetics

Volumn 60, Issue 3, 1996, Pages 201-211

  Gillett, G T ^a,c   Fox, M F ^a   Rowe, P S N ^a,b   Casimir, G M ^a   Povey, S ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b NATIONAL HEALTH SERVICE   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COFILIN;

ARTICLE; CHROMOSOME 11Q; CHROMOSOME 14; CONTROLLED STUDY; GENE MAPPING; HUMAN; HUMAN CELL; HYBRID CELL; MOLECULAR CLONING; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SEQUENCE HOMOLOGY;

EID: 0029740151     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-1809.1996.tb00423.x     Document Type: Article

References (58)

1. ABE, H. & OBIXATA, T. (1989). An actin-depolymerising protein in embryonic chicken-skeletal-muscle: purification and characterization. J. Biochem. (Tokyo) 106, 172-180.
2. ABE, H., ENDO, T., YAMAMOTO, K. & OBIXATA, T. (1990). Sequence of cDNAs encoding actin depolymerizing factor and cofilin of embryonic chicken skeletal muscle : two functionally distinct actin-regulatory proteins exhibit high structural homology. Biochemistry 29, 7420-5.
3. ADAMS, M. D., KERLAVAGE, A. R., FLEISCHMAXX, R.D., FULDXER, R. A., BULT, C. J., LEE, N., KIRKXESS, E. F. & WEIXSTOCK, K. G. et al.. (1995). Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence Nature 377 (Supp.): 3-17.
4. AXDREWS, P., KXOWLES, B. & GOODFELLOW, P. (1981). A human cell-surface antigen defined by a monoclonal antibody and controlled by a gene on chromosome 12. Somat. Cell. Genet. 7, 435-443.
5. BOYD, Y., BUCKLE, V., HOLT, S., MUXRO, B., HUXTER, D. & CRAIG, I. (1987). Molecular heterogeneity of translocations associated with muscular dystrophy. Clin. Genet. 31, 84-91.
6. BURKE, R. D., MA, P. & SMITH, K. D. (1985). Characterization and evolution of a single-copy sequence from the human Y chromosome. Molec. Cell.BioL 5, 576-581.
7. CHIAXG, Y. L., LEY, T. J., SANDERSHAIGH, L. & AXDERsox, W. F. (1984). Human globin gene-expression in hybrid 2s mel × human fibroblast cells. Somal. Cell Mol. Genet. 10, 399-407.
8. COX, D., BUEMEISTER, M., PRICE, E. R., KIM, S. & MYERS, R. M. (1990). Radiation hybrid mapping: a somatic cell genetic method for constructing highresolution maps of mammalian chromosomes. Science 250, 245-250.
9. 2+. Biochem. J. 301, 41-47.
10. DAVIES, R. W., ROBERTS, A. B., JIoRRis, A. J., GRIFFITH, G. W., JERECIC, J., GHAXDI, S., KAISER, K. & SAVIOZ, A. (1994). Enhanced access to rare brain cDNAs by prescreening libraries : 207 new mouse brain ESTs. Genomics 24, 456-463.
11. DE KLEIN, A., VAN KESSEL, A. G., GROSVELD, G., BARTRAM, C. R., HAGEMEIJER, A., BOOTSMA, D., SPURR, X. K., HEISTERKAMP, N., GROFFEX, J. & STEPHEXSON, J. R. (1982). A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia. Nature 300, 765-767.
12. FISHER, J. H., KAO, F. T., JOXES, C., WHITE, R. T., BEXSOX, B. J. & 3IASOX, R. J. (1987). The coding sequence for the 32,000-Dalton pulmonarj- surfactantassociated protein A is located on chromosome 10 and identifies two separate restriction-fragment-length polymorphisms. Am. J. Hum. Genet. 40, 503-511.
13. FLETCHER, J. 31., EVAXS, K., BAILLIE, D., BYED, P., HANRATTY, D., LEACH, S., JULIER, C., GOSDEX, J. R., 3IuiR, W., PORTEOUS, D. J., ST CLAIR, D. & VAX HEYXIXGEX, V. (1993). Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources. Am. J. Hum. Genet. 52, 478-90.
14. GCG. (1994). Program manual for the Wisconsin package. Madison, Genetics Computer Group.
15. GEXEXPRESS. (1995). The Genexpress cDXA program [unpublished]. GenBank, XCBI, Bethesda, USA.
16. GILLETT, G. T., McCoxviLLE, C. 31., BYRD, P. J., STAXKOVIC, T., TAYLOR, A. M., HUNT, D. M., WEST, L. F., Fox, 31. F., POVEY, S. & BEXHAM, F. J. (1993). Irradiation hybrids for human chromosome 11 : characterization and use for generating region-specific markers in 11q14-q23. Genomics 15, 332-341.
17. GLASER, T., HOUSMAX, D., LEWIS, W. H., GERHARD, D. & JOXES, C. (1989). A fine structure deletion map of human chromosome lip: analysis of Jl series hybrids. Somat. Cell Molec. Genet. 15, 477-501.
18. GOODFELLOW, P. X., BANTING, G., TROWSDALE, J., CHAMBERS, S. & SOLOMON, E. (1982). Introduction of a human X-6 translocation chromosome into a mouse teratocarcinoma: investigation of control of H LA-A, B, C expression. Proc. Natl. Acad. Sei. USA 79, 1190-1194.
19. GRIFFO, G., HAMOX-BEXAIS, C., AXGRAXD, P.-O., Fox, 31., WEST, L., LECOQ, O., POVEY, S., CASSIO, D. & WEISS, 31. (1993). HXF4 and HXF1 as well as a panel of hepatic functions are extinguished and reexpressed in parallel in chromosomally reduced rat hepatomahuman fibroblast hybrids. J. Cell BioL 121, 887-898.
20. GUERTS VAX KESSEL, A., TUKCCAKEL, C., DEKLEIN, A., GKOSVELD, G., LENOIR, G. & BOOTSMA, D. (1985). Translocation of oncogene c-sis from chromosome-22 to chromosome-11 in a Ewing sarcoma-derived cellline. Mol. Cell, Biol. 5, 427-429.
21. HUMPHRIES, P., BARTON, D., McKAY, A. M., HUMPHRIES, M. M. & CARRITT, B. (1983). Isolation of a polymorphic DXA segment unique to human chromosome 7 bv molecular cloning of hybrid cell DNA. Mol. Gen. Genet. 190, 143-149.
22. HUNG, W.-Y., DENO, H.-X., HE, X.-X., HENTATI, A. & SIDDIQUE, T. (1994). Localization of cofilin gene to 1q25. (Abstract 204G). Am. J. Hum. Genet. 55, A349.
23. HUNT, D., VAN HEYNINGEN, V., JONES, C., MCONVILLE, C. & BENIIAM, F. J. (1994). Physical mapping of 38 highly informative genetic markers to 10 intervals of chromosome 11q: integration of the physical and genetic maps. Ann. Hum. Genet. 58, 81-85.
24. IlDA, K., MOKIYAMA, K., MATSUMOTO, S., KAWASAKI, H., XISHIDA, E. & YAHARA, I. (1993). Isolation of a yeast essential gene, COF1, that encodes a homologue of mammalian cofilin, a low-M(r) actin-binding and depolymerizing protein. Gene 124, 115-120.
25. JAMES, M. R., RICHARD III, C. W., SCHOTT, J.-J., YOUSRY, C., CLARK, K., BELL, J., TERWILLIGER, J. D., KAZAN, J., DUBAY, C., VIGNAL, A., AGRAPART, M., IMAI, T., NAKAMURA, Y., POLYMEROPOULOS, M., WEISSENBACH, J., Cox, D. R. & LATHROP, G. M. (1994). A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nature Genet. 8, 70-76.
26. JONES, C. & KAO, F. T. (1984). Regional mapping of the folylpolyglutamate synthetase gene (FPGS) to 9cen q34 [abstract]. Cytogenet. Cell Genet. 37, 499-500.
27. 2-microglobulin on human-mouse hybrids. Somal. Cell Genet. 2, 483-496.
28. KAO, F. T., JONES C. & PUCK, T. T. (1976). Genetics of somatic mammalian cells. Genetic, immunologie, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes. Proc. Natl. Acad. Sei. USA 73, 193-197.
29. KIELTY, C. M., POVEY, S. & HOPKINSON, D. A. (1982). Regulation of expression of liver specific enzymes, III. Further analysis of a series of rat hepatoma and human somatic cell hybrids. Ann. Hum. Genet. 46, 307-327.
30. KOEFFLER, H. P., SPARKES, R. S., STANG, H. & MOHANDAS, T. (1981). Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome-16. Proc. Natl. Acad. Sei. USA 78, 7015-7018.
31. LARSSON, C., SKOGSEID, B., OBERG, K., XAKAMURA, Y. & XORDENSKJOLD, M. (1988). Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 332, 85-87.
32. MATSUZAKI, F., MATSUMOTO, S., YAHARA, I., YONEZAWA, N., NISHIDA E. & SAKAI, H. (1988). Cloning and characterization of porcine brain cofilin cDXA. Cofilin contains the nuclear transport signal sequence. J. liiol. Cliem. 263, 11564-11568.
33. MOON, A. L., JANMEY, P. A., LOUIE, K. A. & DRUBIN, D. G. (1993). Cofilin is an essential component of the yeast cortical cytoskclcton. J. Cell Biol. 120, 421-435.
34. MORIYAMA, K., MATSUMOTO, S., XlSHIDA, E., SAKAI, H. & YAHARA, I. (1990). Nucleotide sequence of mouse cofilin cDXA. Nucleic Adds Res. 18, 3053.
35. MULLEY, J. C. & CALLEN, D. F. (1980). New regional localisations for HAGH and PGP on human chromosome 16. Hum. Genet. 74, 423-424.
36. MUXEYUKI, F., NlSHIDA, E., SUTOH, K. & SAKAI, H. (1985). Purification of cofilin, a 21,000 molecularweight actin-binding protein, from porcine kidney and identification of the cofilin-binding site in the actin sequence. J. Biocfiem. 97, 503-568.
37. NAGARAJAX, L., LOUIE, E., TSUJIMOTO, Y., ARRUSHDI, A., HUEBXER K. & CROCE, G. M. (1980). Localization of the human PIM oncogene (PIM) to a region of chromosome 6 involved in translocations in acute leukemias. Proc. Natl. Acad. Sei. USA 83, 2556-2500.
38. NIGMS. (1994). 1994/1995 Catalog of Cell Lines. National Intitules of Health, US Department of Health and Human Services, Bethesda.
39. NISHIDA, E., MAEKAWA, S. & SAKAI, H. (1984). Cofilin, a protein in porcine brain that binds to actin-filaments and inhibits their interactions with myosin and tropomyosin. Biochemistry 23, 5307-5313.
40. NISHIDA, E., IIDA, K., YOXEZAWA, N., KOYASU, S., YAHARA, I. & SAKAI, H. (1987). Cofilin is a component of intranuclear and cytoplasmic actin rods induced in cultured-cells. Proc. Nail. Acad. Sei. USA 84, 5262-5266.
41. NIZETIC, D., ZEHETNER, G., MONACO, A. P., GELLEN, L., Youxo, B. D. & LEHRACH, H. (1991). Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries. Proc. Null. Acad. Sei. USA 88, 3233-3237.
42. OGAWA, K., TASHIMA, M., YUMOTO, Y., OKUDA, T., SAWADA, H., OKUMA, M. & MARUYAMA, Y. (1990). Coding sequence of human placenta cofilin cDNA. Nucleic Acids Res. 18, 7169.
43. OHTA, Y., NISHIDA, E., SAKAI, H. & MIYAMOTO, E. (1989). Dephosphorylation of cofilin accompanies heat shock-induced nuclear accumulation of cofilin. J. Biol. Chem. 264, 10143-10148.
44. ONO, S., MINAMI, N., ABE, H. & OBINATA, T. (1994). Characterization of a novel cofilin isoform that is predominantly expressed in skeletal muscle. J. Biol. Chem. 269, 15280-15286.
45. PORTEOUS, D., WlLKINSON, M., FLETCHER, J. & VAX HEYNINGEN, V. (1989). Human mouse hybrids carrying fragments of single human chromosomes selected by tumour growth. Genomics 5, 680-684.
46. PURDUE, P. E., LUMB, M. J., Fox, M., GRIFFO, G., HAMON-BENAIS, C., POVEY, S. & DANPURE, C. J. (1991). Characterization and chromosomal mapping of a genomic clone encoding human alanine: glyoxalate aminotransferase. Genomics 10, 34-42.
47. RICHARD, C. W., WITHERS, D. A., MEEKER, T. C., MAURER, S., EVANS, G. A., MYERS, K. M. & Cox, D. R. (1991). A radiation hybrid map of the proximal long arm of human chromosome 11 containing the MEN-1 and bcl-1 disease loci. Am. J. Hum. Genet. 49, 1189-1196.
48. SACCHI, N., WATSON, D. K., VAN KESSEL, A. H. M. G., HAGEMEIJER, A., KERSEY, J., DKABKIN, H. D., PATTERSOX, D. & PAPAS, T. S. (19S6). Hu-ets-l and hu-ets-2 genes arc transposed in acute leukemias with (4-11) and (8-21) transloeations. Science 231, 379-382.
49. SAMSTAG, Y., ECKERSKORN, C., WESSELBORG, S., HENNING, S., WALLICH, R. & MEUER, S.O. (1994). Costimulatory signals for human T-cell activation induce nuclear translocation of ppl9/cofilin. Proc. Nail. Acad. Sei. USA 91, 4494-8.
50. SHIRASAWA, T., TAKAHASHI, H., SAKAMOTO, K., KAWASHIMA, A. & AKASHI, T. (1991). Xuclcotide sequence of the rat cofilin cDXA [unpublished]. GenBank, NCBI, Bethesda, USA.
51. SOLOMON, E., SWALLOW, D. M., BURGESS, S. & EVANS, L. (1979). Assignment of the human acid α-glucosidase gene (α GLU) to chromosome 17 using somatic cell hybrids. Ann. Hum. Genet. 42, 273-281.
52. SWALLOW, D. M., GENOLER, S., GRIFFITHS, B., KEARNEY, A., POVEY, S., SHEER, D., PALMER, R. \V. & TAYLOR-PAPADIMITRIOU, J. (1987). The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region lq21-24. Ann. Hum. Genet. 51, 289-294.
53. WILLIAMS, B. P., SHIPLEY, J. P., SPURR, N. K., SMITH, D. R., HAYMAN M. J. & GOODFELLOW, P. N. (1988). A human sequence homologous to vsea maps to chromosome 11, band q!3. Oncogene 3, 345-348.
54. WOXG, Z., WILSON, V., I'ATEL, I., POVEY, S. & JEFFREYS, A. J. (1987). Characterization of a panel of highly variable minisatellites cloned from human DNA. Ann Hum. Genet. 51, 269-288.
55. YONEZAIVA, N., NISHIDA, E. & SAKAI, H. (1985). Ph control of actin polymerization bv cofilin. J. Biol. Chem. 260, 4410-4412.
56. YONEZAWA, N., NISHIDA, E., IIDA, K., YAHARA, I. & SAKAI, H. (1990). Inhibition of the interactions of cofilin, destrin, and deoxyribonuclease I with actin by phosphoinositides. J. DioL Chem. 265, 8382-8380.
57. YONEZAWA, N., HOMMA, Y., YAHARA, I., SAKAI, H. & NISHIDA, E. (1991). A short sequence responsible for both phosphoinositide binding and actin binding activities of cofilin. J. Biol. Chem. 266, 17218-17221.
58. ZHONG, S., WOLF, C. R. & SPURR, X. (1992). Chromosomal assignment and linkage analysis of the human glutathione S-transferase μ gene (GSTM1) using intron specific polymerase chain reaction. Hum. Genet. 90, 435-439.