Genetic analyses of Tattered, an X-linked dominant, developmental mouse mutation

Springer Science and Business Media LLC - Tập 6 Số 4 - Trang 291-294 - 1995
Kevin Merrell1, Juanita C. Gonzales2, Sandra M. Wells3, Kathryn Calame3, Gail E. Herman2
1Integrated Program in Molecular Biology and Cellular Biophysics, Columbia College of Physicians and Surgeons, New York, New York, USA
2Department of Molecular and Human Genetics, One Baylor Plaza 821T, 77030, Houston, Texas, USA
3Department of Microbiology, Columbia College of Physicians and Surgeons, New York, New York, USA

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Blair, H.J., Boyd, Y. (1994). Positioning of 14 simple sequence repeat loci relative to markers on the gene-based map of the mouse X chromosome. Mouse Genome 92, 127?129.

Blair, H.J., Reed, V., Laval, S.H., Boyd, Y. (1994a). New insights into the man-mouse comparative map of the X chromosome. Genomics 19, 215?220.

Blair, P.J., Carpenter, D.A., Godfrey, V.L., Russell, L.B., Rinchik, E.M. (1994b). The scurfy (sf) mutation is tightly linked to Gatal/Tfe3 on the proximal X chromosome. Mamm. Genome 5, 652?654.

Brown, S.D.M., Avner, P., Boyd, Y., Chapman, V., Rastan, S., Sefton, L., Thomas, J.D., Herman, G.E. (1993). Mouse X Chromosome. Mamm. Genome 4 (Suppl.), S269-S281.

Cattanach, B.M. (1982a). A new X-linked mutation. Mouse News Lett 66, 61?62.

Cattanach, B.M. (1982b). Location of tattered (Td). Mouse News Lett. 67, 19.

Chirgwin, J.M., Przybyla, A.E., MacDonald, R.J., Rutter, W.J. (1979). Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18, 5294?5299.

Cremin, S.M., Greer, W.L., Bodok-Nutzati, R., Schwartz, M., Peacocke, M., Siminovitch, K.A. (1993). Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region. Hum. Genet. 92, 250?253.

Derry, J.M.J., Ochs, H.D., Francke, U. (1994). Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 78, 635?644.

Faust, C.J., Herman, G.E. (1991). Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28. Genomics 11, 154?164.

Glover, T.W., Verga, V., Rafael, J., Barcroft, C., Gorski, J.L., Bawle, E.V., Higgins, J.V. (1993). Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Hum. Mol. Genet. 2, 1717?1718.

Herman, G.E., Walton, S.J. (1990). Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics 7, 307?312.

Hodgkinson, C.A., Moore, K.J., Nakayama, A., Steingrimsson, E., Copeland, N.G., Jenkins, N.A., Arnheiter, H. (1993). Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74, 395?404.

Kantor, A.B., Stall, A.M., Adams, A., Herzenberg, L.A., Herzenberg, L.A. (1992). Differential development of progenitor activity for three B cell lineages. Proc. Natl. Acad. Sci. USA 89, 3320?3324.

Laval, S.H., Boyd, Y. (1993). Partial inversion of gene order within a homologous segment on the X Chromosome. Mamm. Genome 4, 119?123.

Nahm, M.H., Paslay, J.W., Davie, J.M. (1983). Unbalanced X chromosome mosaicism in B cells of mice with X-linked immunodeficiency. J. Exp. Med. 158, 920?931.

Pevny, L., Simon, M.C., Robertson, E., Klein, W.H., Tsai, S.-F., D'Agati, V., Orkin, S.H., Constantini, F. (1991). Erythroid differentiation in chimaeric mice blocked by a targeted gene mutation for transcription factor GATA1. Nature 349, 257?260.

Rawlings, D.J., Saffran, D.C., Tsukada, S., Largaespada, D.A., Grimaldi, J.C., Cohen, L., Mohr, R.N., Bazan, F., Howard, M., Copeland, N.G., Jenkins, N.A., Witte, O.N. (1993). Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice. Science 261, 358?361.

Roman, C., Lohn, L., Calame, K. (1991). Creation of a trans-dominant negative form of transcription activator in TFE3 by differential splicing. Science 254, 94?97.

Roman, C., Matera, A.G., Cooper, C., Artandi, S., Blain, S., Ward, D.C., Calame, K. (1992). mTFE3, an X-linked transcriptional activator containing basic helix-loop-helix and zipper domains, utilizes the zipper to stabilize both DNA binding and multimerization. Mol. Cell. Biol. 12, 817?827.

Sybert, V.P. (1994). Incontinentia pigmenti nomenclature. Am. J. Hum. Genet. 55, 209?211.

Thomas, J.D., Sideras, P., Edward Smith, C.I., Vorechovsky, I., Chapman, V., Paul, W.E. (1993). Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes. Science 261, 355?358.