Abstract
We present here the genetic mapping of the α-skeletal actin locus (Actsk-1) on mouse Chromosome (Chr) 8, on the basis of the PCR analysis of a microsatellite in an interspecific backcross. Linkage and genetic distances were established for four loci by analysis of 192 (or 222) meiotic events and indicated the following gene order: (centromere)-Es-1-11.7 cM-Tat-8.3 cM-Actsk-1-0.5 cM-Aprt. Mapping of ACTSK to human Chr 1 and of TAT and APRT to human Chr 16 demonstrates the existence of a new short region of homology between mouse Chr 8 and human Chr 1. Intermingling on this scale between human and mouse chromosomal homologies that occurred during evolution creates disorders in comparative linkage studies.
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Abonia, J.P., Abel, K.J., Eddy, R.L., Elliott, R.W., Chapman, V.M., Shows, T.B., and Gross, K.W.: Linkage of Agt and Actsk-1 to distal mouse Chromosome 8 loci: a new conserved linkage. Mammalian Genome 4: 25–32, 1993.
Alonso, S., Garner, I., Vandekerckhove, J., and Buckingham, M.: A genetic analysis of the interaction between cardiac and skeletal actin gene expression in striated muscle of the mouse. J Mol Biol 211: 727–738, 1990.
Barton, D.E., Yang-Feng, T.L., and Francke, U.: The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22-q24) by somatic cell hybrid analysis and in situ hybridization. Hum Genet 72: 221–224, 1986.
Ceci, J.D.: Mouse Chromosome 8. Mammalian Genome 1 (Suppl): S112-S126, 1991.
Chien-Tsung Hu, M., Sharp, S.B., and Davidson, N.: The complete sequence of the mouse skeletal α-actin gene reveals several conserved and inverted repeat sequences outside of the protein-coding region. Mol Cell Biol 6: 15–25, 1986.
Clouston, W.M., Fournier, R.E.K., and Richards, R.I.: The angiotensinogen gene is located on mouse chromosome 8. FEBS Lett 255: 419–422, 1989.
Crosby, J.L., Phillips, S., and Nadeau, J.H.: The cardiac actin locus (Actc-1) is not on mouse chromosome 17 but is linked to β2-microglobulin on chromosome 2. Genomics 5: 19–23, 1989.
Czosnek, H., Nudel, U., Shani, M., Barker, P.E., Pravtcheva, D.D., Ruddle, F.H., and Yaffe, D.: The genes coding for the muscle contractile proteins, myosin heavy chain, myosin light chain 2, and skeletal muscle actin are located on three different mouse chromosomes. EMBO J 1: 1299–1305, 1982.
Czosnek, H., Nudel, U., Mayer, Y., Barker, P.E., Pravtcheva, D.D., Ruddle, F.H., and Yaffe, D.: The genes coding for the cardiac muscle actin, the skeletal muscle actin and the cytoplasmic β-actin are located on three different mouse chromosomes. EMBO J 2: 1977–1979, 1983.
Dush, M.K., Sikela, J.M., Khan, S.A., Tischfield, J.A., and Stambrook, P.J.: Nucleotide sequence and organization of the mouse adenine phosphoribosyltransferase gene: presence of a coding region common to animal and bacterial phosphoribosyl-transferases that has a variable intron/exon arrangement. Proc Natl Acad Sci USA 82: 2731–2735, 1985.
Guénet, J.-L., Simon-Chazottes, D., and Avner, P.R.: The use of interspecific mouse crosses for gene localization: present status and future perspectives. Curr Top Microbiol Immunol 137: 13–17, 1988.
Gunning, P., Ponte, P., Kedes, L., Eddy, R., and Shows, T.: Chromosomal location of the co-expressed human skeletal and cardiac actin genes. Proc Natl Acad Sci USA 81: 1813–1817, 1984.
Hanauer, A., Levin, M., Heilig, R., Daegelen, D., Khan, A., and Mandel, J.-L.: Isolation and characterization of cDNA clones for human skeletal muscle α actin. Nucleic Acids Res 11: 3503–3516, 1983.
Hidaka, Y., Tarlé, S.A., O'Toole, T.E., Kelley, W.N., and Palella, T.D.: Nucleotide sequence of the human APRT gene. Nucleic Acids Res 15: 9086–9086, 1987.
Howard, T.A., Rochelle, J.M., Saunders, A.M., and Seldin, M.F.: A linkage map of mouse chromosome 8: further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19. Genomics 10: 207–213, 1991.
Humphries, S.E., Whittall, R., Minty, A., Buckingham, M., and Williamson, R.: There are approximately 20 actin genes in the human genome. Nucleic Acids Res 9: 4895–4908, 1981.
Isa, M.N., Boyd, E., Morrison, N., Harrap, S., Clauser, E., and Connor, J.M.: Assignment of the human angiotensin gene to chromosome 1q42-q43 by nonisotopic in situ hybridization. Genomics 8: 598–600, 1990.
Julier, C., Nakamura, Y., Lathrop, M., O'Connell, P., Leppert, M., Mohandas, T., Lalouel, J.-M., and White, R.: A primary map of 24 loci on human chromosome 16. Genomics 6: 419–427, 1990.
Lyon, M.F., and Kirby, M.C.: Mouse chromosome atlas. Mouse Genome 90(1): 22–44, 1992.
Minty, A.J., Alonso, S., Caravatti, M., and Buckingham, M.E.: A fetal skeletal muscle actin mRNA in the mouse and its identity with cardiac actin mRNA. Cell 30: 185–192, 1982.
Minty, A.J., Alonso, S., Guénet, J.-L., and Buckingham, M.E.: Number and organization of actin-related sequences in the mouse genome. J Mol Biol 167: 77–101, 1983.
Montagutelli, X.: Gene-link: a program in Pascal for backcross genetic linkage analysis. J Hered 81: 490–491, 1990.
Müller, G., Scherer, G., Zentgraf, H., Ruppert, S., Herrmann, B., Lehrach, H., and Schütz G.: Isolation, characterization and chromosomal mapping of the mouse tyrosine aminotransferase gene. J Mol Biol 184: 367–373, 1985.
Muscat, G.E.O., Gustafson, T.A., and Kedes, L.: A common factor regulates skeletal and cardiac α-actin gene transcription in muscle. Mol Cell Biol 8: 4120–4133, 1988.
Nadeau, J.H., Davisson, M.T., Doolittle, D.P., Grant, P., Hillyard, A.L., Kosowsky, M., and Roderick, T.H.: Comparative map for mice and humans. Mammalian Genome 1 (Suppl): S461-S515, 1991.
Nesterova, T.B., Borodin, P.M., Zakian, S.M., and Serov, O.L.: Assignment of the gene for adenine phosphoribosyltransferase on the genetic map of mouse chromosome 8. Biochem Genet 25: 563–568, 1987.
Ponte, P., Gunning, P., Blau, H., and Kedes, L.: Human actin genes are single copy for α-skeletal and α-cardiac actin but multicopy for β- and γ-cytoskeletal genes: 3′ untranslated regions are isotype specific but are conserved in evolution. Mol Cell Biol 3: 1783–1791, 1983.
Robert, B., Barton, P., Minty, A., Daubas, P., Weydert, A., Bonhomme, F., Catalan, J., Chazottes, D., Guénet, J.-L., and Buckingham, M.: Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross. Nature 314: 181–183, 1985.
Scherer, G., Bausch, E., Gaa, A., and von Deimling, O.: Gene mapping on mouse chromosome 8 by interspecific crosses: new data on a linkage group conserved on human chromosome 16q. Genomics 5: 275–282, 1989.
Smeets, H.J.M., Brunner, H.G., Ropers, H.H., and Wieringa, B.: Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy. Hum Genet 83: 245–251, 1989.
Soriano, P., Szabo, P., and Bernardi, G.: The scattered distribution of actin genes in the mouse and human genomes. EMBO J 1: 579–583, 1982.
Vandekerckhove, J. and Weber, K.: The complete amino acid sequence of actins from bovine aorta, bovine heart, bovine fast skeletal muscle, and rabbit slow skeletal muscle. Differentiation 14: 123–133, 1979.
Yap, E.P.H. and O'D.McGee, J.: Short PCR product yields improved by lower denaturation temperatures. Nucleic Acids Res 19: 1713, 1991.
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Alonso, S., Montagutelli, X., Simon-Chazottes, D. et al. Re-localization of Actsk-1 to mouse Chromosome 8, a new region of homology with human Chromosome 1. Mammalian Genome 4, 15–20 (1993). https://doi.org/10.1007/BF00364657
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DOI: https://doi.org/10.1007/BF00364657