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Assignment of the mouse desmin gene to chromosome 1 band C3

Published online by Cambridge University Press:  14 April 2009

Zhenlin Li ,
Marie-Geneviève Mattei ,
Jean-François Mattei  and
Denise Paulin
Zhenlin Li
Affiliation:
Laboratoire de Biologie Moléculaire de la Différenciation de l'Université Paris 7 et de l'Institut Pasteur – 25, rue du Docteur Roux – 75754, Paris
Marie-Geneviève Mattei
Affiliation:
INSERM U. 242 Centre de génétique médicale, Hôpital d'enfants de la Timone, 13385 Marseille Cedex, France
Jean-François Mattei
Affiliation:
INSERM U. 242 Centre de génétique médicale, Hôpital d'enfants de la Timone, 13385 Marseille Cedex, France
Denise Paulin*
Affiliation:
Laboratoire de Biologie Moléculaire de la Différenciation de l'Université Paris 7 et de l'Institut Pasteur – 25, rue du Docteur Roux – 75754, Paris
*
Corresponding author: Denise Paulin, Institut Pasteur SCME, 25 rue du Dr Roux, 75015 Paris.
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Summary

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The chromosomal localization of the mouse gene coding for desmin, one of the muscle-specific intermediate filament subunits, was determined by in situ hybridization using a specific 3H-labelled DNA probe. There is only one copy of the desmin gene and it is located on chromosome 1 in the band C3. This result adds an eleventh locus to a conserved gene cluster and confirms the partial homology that exists between the long arm of human chromosome 2 and chromosome 1 of the mouse.

Type
Research Article
Information
Genetics Research , Volume 55 , Issue 2 , April 1990 , pp. 101 - 105
Copyright
Copyright © Cambridge University Press 1990

References

Barton, D. E., Yan-Feng, T. L., Mason, A. J., Seeburg, P. H. & Francke, U. (1987). INHA, INHBA and INHBB. The loci for the three subunits of inhibin, mapped in mouse and man. Cytogenetics and Cell Genetics 46, 578.Google Scholar
Berger, R., Bloomfield, C. D. & Sutherland, G. R. (1985). Report on the committee on chromosome rearrangements in neoplasia and on fragile sites (Eighth International Workshop on Human Gene Mapping). Cytogenetics and Cell Genetics 40, 490–535.CrossRefGoogle Scholar
Brunet, J. F., Denizot, F., Luciani, M. F., Roux-Dosseto, M., Suzan, M., Mattei, M. G. & Golstein, P. (1987). A new member of the immunoglobulin superfamily CTLA- 4. Nature 328, 267–270.CrossRefGoogle ScholarPubMed
Buckle, V. J., Edwards, J. H., Evans, E. P., Jonasson, J. A., Lyon, M. F., Peters, J., Searle, A. G. & Wedd, N. S. (1984). Chromosome maps of man and mouse II. Clinical Genetics 26, 1–11.CrossRefGoogle ScholarPubMed
Chan, D., Goate, A. & Puck, T. (1989). Involvement of vimentin in the reverse transformation reaction. Proceedings of the National Academy of Sciences USA 86, 2747–2751.CrossRefGoogle ScholarPubMed
Cleveland, D. W., Hughes, S. H., Stubblefield, E., Kirschner, M. W. & Varmus, H. E. (1981). Multiple a and β tubulin genes represent unlinked and dispersed gene families. Journal of Biological Chemistry 256, 3130–3134.CrossRefGoogle ScholarPubMed
Cohen-Haguenauer, O., Barton, P. J. R., Merlie, J., Van Cong, N., Masset, M., de Tand, M. F. & Frezal, J. (1987). Localization of the human acetylcholine receptor gamma subunit gene to 2q32-qter. Cytogenetics and Cell Genetics 46, 595.Google Scholar
Dariavach, P., Mattei, M. G., Golstein, P. & Lefranc, M. P. (1988). Human Ig superfamily CTLA-4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains. European Journal of Immunology 18, 1901–1905.CrossRefGoogle ScholarPubMed
Dautigny, A., Pham-Dinh, D., Rouselle, G., Felix, J. L., Nussbaum, J. L. & Jolles, P. (1988). The large neurofilament subunit (NF-H). cDNA cloning and in situ detection. Biochemical and Biophysical Research Communications 154, 1099–1106.CrossRefGoogle ScholarPubMed
Ferrari, S., Battini, R., Kaczmarek, L., Rittling, S., Calabretta, B., De Reil, J. K., Philiponis, V., Wei-Fang, J. & Baserga, R. (1986). Coding sequence and growth regulation of the human vimentin gene. Molecular and Cellular Biochemistry 6, 3614–3620.Google ScholarPubMed
Ferrari, S., Cannizzaro, L. A., Batini, R., Huebner, K. & Baserga, R. (1987). The gene encoding human vimentin is located on the short arm of chromosome 10. American Journal of Human Genetics 41, 616–626.Google ScholarPubMed
Hanauer, A., Heilig, R., Levin, M., Moisan, J. P., Grzeschik, K. H. & Mandel, J. L. (1984). The actin gene family in man: assignment of the gene for skeletal muscle alpha- actin to chromosome 1, and presence of actin sequences on autosome 2 and 3, and on the X and Y chromosomes. Cytogenetics and Cell Genetics 37, 487–488.Google Scholar
Heidmann, O., Buonanno, A., Geoffrey, B., Robert, B., Guénet, J. L., Merlie, J. P. & Changeux, J. P. (1986). Chromosomal localization of muscle nicotinic acetylcholine receptor genes in the mouse. Science 234, 866–868.CrossRefGoogle ScholarPubMed
Hurst, J., Flavell, D., Julien, J. P., Meijer, P., Mushinski, W. & Grosveld, F. (1987). The human neurofilament gene (NF-L) is located on the short arm of chromosome 8. Cytogenetics and Cell Genetics 45, 30–32.CrossRefGoogle Scholar
Jhanwar, S. C, Jensen, J. T., Kaelbling, M., Chaganti, R. S. K. & Klinger, H. P. (1986). In situ localization of human fibronectin (FN) genes to chromosome regions 2q14-p16, 2q34-q36, and 11q12·1-q13·5 in germ line cells, but to chromosome 2 sites only in somatic cells. Cytogenetics and Cell Genetics 41, 47–53.CrossRefGoogle ScholarPubMed
Julien, J. P., Grosveld, F., Yazdanaksh, K., Flavell, D., Meijer, D. & Mushynski, W. E. (1987). The structure of a human neurofilament gene (NF-L) a unique exonintron organization in the intermediate filament gene family. Biochimica et Biophysica Acta 909, 10–20.CrossRefGoogle ScholarPubMed
Klinge, E. M., Sylvestre, Y. R., Freedberg, I. M. & Blumenberg, M. (1987). Evolution of keratin genes: different protein domains evolve by different pathways. Journal of Molecular Evolution 24, 319–329.CrossRefGoogle ScholarPubMed
Lalley, P. A., Davisson, M. T., Graves, J. A. M., O'Brien, S. J., Womack, J. E., Roderick, T. H., Creau-Goldberg, N., Hillyard, A. L., Doolittle, D. P. & Rogers, J. A. (1989). Report of the committee on comparative mapping (Tenth International Workshop on Human Gene Mapping). Cytogenetics and Cell Genetics 51, 503–532.CrossRefGoogle Scholar
Landon, F., Lemonnier, M., Benarous, R., Huc, C., Fiszman, M., Gros, F. & Portier, M. M. (1989). Multiple mRNA encode peripherin, a neuronal intermediate filament protein. EMBO Journal 8, 1719–1726.CrossRefGoogle ScholarPubMed
Leonard, W., Donlon, T. A., Lebo, R. V. & Green, W. C. (1985). Localization of the gene encoding the human interleukin-2 receptor on chromosome 10. Science 228, 1542–1549.CrossRefGoogle ScholarPubMed
Lewis, S. A., Balcarek, J. M., Krek, V., Shelanski, M. & Cowan, N. J. (1984). Sequence of a cDNA clone encoding mouse glial fibrillary acidic protein: structural conservation of intermediate filaments. Proceedings of the National Academy of Sciences USA 81, 2743–2746.CrossRefGoogle ScholarPubMed
Li, Z., Lilienbaum, A., Buttler-Browne, G. & Paulin, D. (1989). Human desmin coding gene: complete nucleotide sequence, characterization and regulation of expression during myogenesis and development. Gene 78, 242–254.Google ScholarPubMed
Lieberburg, I., Spinner, N., Snyder, S., Anderson, J., Goldaber, D., Smulowitz, N., Carrol, Z., Emmanuel, B., Breitner, J. & Rubin, L. (1989). Cloning of a cDNA encoding the high molecular weight neurofilament peptide (NF-H), Development and tissue expression in the rat and mapping of its human homologue to chromosomes 1 and 22. Proceedings of the National Academy of Sciences USA 86, 2463–2467.CrossRefGoogle ScholarPubMed
Lilienbaum, A., Li, Z., Butler-Browne, G., Bolmont, C., Grimaud, J. A. & Paulin, D. (1988). Human desmin gene: utilization as a marker of human muscle differentiation. Cellular and Molecular Biology 34, 663–672.Google ScholarPubMed
Lobos, E. A., Rudnick, C. H., Watson, M. S. & Isenberg, K. E. (1989). Linkage disequilibrium study of RFLPs detected at the human muscle nicotinic acetylcholine receptor subunit genes. American Journal of Human Genetics 44, 522–533.Google ScholarPubMed
Mattei, M. G., Philip, N., Passage, E., Moisan, J. P., Mandel, J. L. & Mattei, J. F. (1985). DNA probe localization at 18 p113 band by in situ hybridization and identification of a small supernumerary chromosome. Human Genetics 69, 268–271.CrossRefGoogle ScholarPubMed
Mattei, M. G., Dautigny, A., Pham-Dinh, D., Passage, E., Mattei, J. F. & Jolles, P. (1988). The gene encoding for the large human neurofilament subunit (NF-H) maps to the q12·1-q13·l region on the human chromosome 22. Human Genetics 80, 293–295.CrossRefGoogle Scholar
Mattei, M. G., Lilienbaum, A., Li, Z., Mattei, J. F. & Paulin, D. (1989). Chromosome localization of the mouse gene coding for the vimentin. Genetical Research 53, 183–185.CrossRefGoogle ScholarPubMed
Mattei, M. G., Duprey, P., Li, Z., Mattei, J. F. & Paulin, D. (1989). Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunit. Journal of Cell Biology, in press.Google ScholarPubMed
Moll, R., Franke, W. W., Schiller, D. L., Geiger, B. & Krepler, R. (1982). The catalog of human cytokeratins: patterns of expression in normal epithelial, tumors and cultured cells. Cell 31, 11–24.CrossRefGoogle ScholarPubMed
Narahara, K., Kimura, S., Kikkawa, K., Takahashi, Y., Wakita, Y., Kasai, R., Nagai, S., Nishibayashi, Y. & Kimoto, H. (1985). Probable assignment of soluble isocitrate dehydrogenase (IDH1) to 2q33–3. Human Genetics 71, 37–40.CrossRefGoogle ScholarPubMed
Perreau, J., Lilienbaum, A., Vasseur, M. & Paulin, D. (1988). Nucleotide sequence of the human vimentin gene and regulation of its transcription in tissues and cultured cells. Gene 62, 7–16.CrossRefGoogle ScholarPubMed
Quax, W., Van Der Heuvel, R., Vree Egberts, W., Quax-Jeuken, Y. & Bloemendal, H. (1984). Intermediate filament cDNAs from BHK-21 cells: demonstration of distinct genes for desmin and vimentin in all vertebrate classes. Proceedings of the National Academy of Sciences USA 81, 5970–5974.CrossRefGoogle ScholarPubMed
Quax, W., Meera Khan, P., Quax-Jeuken, Y. & Bloemendal, H. (1985). The human desmin and vimentin genes are located on different chromosomes. Gene 38, 189–196.CrossRefGoogle ScholarPubMed
Quax, W., Vree Egberts, W., Hendriks, W., Quax-Jeuken, Y. & Bloemendal, H. (1983). The structure of the vimentin gene. Cell 35, 215–223.CrossRefGoogle ScholarPubMed
Robert, B., Barton, P., Minty, A., Daubas, P., Weydert, A., Bonhomme, F., Catalan, J., Chazottes, D., Guénet, J. L. & Buckingham, M. (1985). Investigation of genetic linkage between myosin and actin genes using an interspecific backcross. Nature 314, 181–183.CrossRefGoogle Scholar
Rousseau-Merck, M. F., Simon-Chazottes, D., Arpin, M., Pringault, E., Louvard, D., Guénet, J. L. & Berger, R. (1988). Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1. Human Genetics 78, 130–133.CrossRefGoogle ScholarPubMed
Seldin, M. F., Kingsmore, S. F. & Moseley, W. S. (1989). Analyses of gene linkage relationships in the mouse using an interspecific cross: comparative mapping of genes localized to human chromosome 1. Human Gene Mapping 10. Ed. Karger, F.Google Scholar
Shiloh, Y., Donlon, T., Bruns, G., Breitman, M. L. & Tsui, L.-C. (1986). Assignment of the human gamma-crystallin gene cluster (Cryg) to the long arm of chromosome 2, region q33–36. Human Genetics 73, 17–19.CrossRefGoogle Scholar
Skow, L. C, Adkison, L., Womack, J. E., Beamer, W. G. & Taylor, B. A. (1987). Mapping of the mouse fibronectin gene to chromosome 1. Conservation of the Idh-1-Cryg Fn synteny group in mammals. Genomics 1, 283, 286.CrossRefGoogle ScholarPubMed
Serero, S., Barton, P., Van Cong., N., Cohen-Haguenauer, O., Robert, B., Buckingham, P. & Frezal, J. (1987). Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLS3F) to 2q321- 2qter. Cytogenetics and Cell Genetics 46, 690.Google Scholar
Solomon, E., Hiorns, L. R., Spurr, N., Kurkien, M., Barlow, D. & Hogan, B. L. M. (1985). Chromosomal assignments of the genes coding for human types II, III and IV collagen: a dispersed gene family. Proceedings of the National Academy of Sciences USA 82, 3330–3334.CrossRefGoogle ScholarPubMed
Soriano, P., Szabo, P. & Bernardi, G. (1982). The scattered distribution of actin genes in the mouse and human genomes. EMBO Journal 1, 579–583.CrossRefGoogle ScholarPubMed
Steinert, P. M., Steven, A. C. & Roop, D. R. (1985). The molecular biology of intermediate filaments. Cell 42, 411–419.CrossRefGoogle ScholarPubMed
Viegas-Péquignot, E., Li, Z., Dutrillaux, B., Apiou, F. & Paulin, D. (1989). Assignment of human desmin gene to band 2q35 by non radioactive in situ hybridization. Human Genetics 83, 33–36.CrossRefGoogle Scholar
Zehner, Z. E. & Paterson, B. M. (1983). Characterization of the 15 chicken vimentin gene: single copy gene producing multiple mRNAs. Proceedings of the National Academy of Sciences USA 80, 911–915.CrossRefGoogle Scholar
Zneimer, S. M. & Womack, J. E. (1988). Comparative chromosomal localization of the fibronectin and gamma crystallin genes in three mammalian species: human, mouse and cow. American Journal of Human Genetics 43, (Suppl): A164.Google Scholar