This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Robbins, J
Right arrow Articles by Callahan, R
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Robbins, J
Right arrow Articles by Callahan, R

 Previous Article

J Virol. 1992 April; 66(4): 2594-2599

Mouse mammary tumor gene int-3: a member of the notch gene family transforms mammary epithelial cells.

J Robbins, B J Blondel, D Gallahan and R Callahan

Laboratory of Tumor Immunology and Biology, National Cancer Institute, Bethesda, Maryland 20892.

ABSTRACT

Expression of a 2.3-kb RNA species is induced in mammary tumors as a consequence of insertional mutagenesis at the int-3 locus by the mouse mammary tumor virus. The nucleotide sequence and biological activity of this mammary tumor-specific int-3 RNA species were determined. It contains an open reading frame which encodes a 57-kDa protein. The translated protein possesses six nearly contiguous 32-amino-acid repeats which are related to a similar motif in the Saccharomyces cerevisiae cdc-10-encoded cell cycle protein. In addition, the int-3 cdc-10 repeats are bounded by the PEST amino acid sequence motif which is commonly found in proteins having a rapid turnover and may represent sites for phosphorylation. The int-3 cdc-10 repeat sequences are 50% identical to a portion of the intracellular domain of the neurogenic Drosophila notch gene product. Activation of expression of a recombinant int-3 genomic DNA fragment encoding the 2.3-kb RNA species in HC11 mouse mammary epithelial cells in vitro induces anchorage-independent growth in soft agar.


J Virol. 1992 April; 66(4): 2594-2599




This article has been cited by other articles:

  • Theodosiou, A., Arhondakis, S., Baumann, M., Kossida, S. (2009). Evolutionary Scenarios of Notch Proteins. Mol Biol Evol 26: 1631-1640 [Abstract] [Full Text]  
  • Luther, K. B., Schindelin, H., Haltiwanger, R. S. (2009). Structural and Mechanistic Insights into Lunatic Fringe from a Kinetic Analysis of Enzyme Mutants. J. Biol. Chem. 284: 3294-3305 [Abstract] [Full Text]  
  • Yamaguchi, N., Oyama, T., Ito, E., Satoh, H., Azuma, S., Hayashi, M., Shimizu, K., Honma, R., Yanagisawa, Y., Nishikawa, A., Kawamura, M., Imai, J.-i., Ohwada, S., Tatsuta, K., Inoue, J.-i., Semba, K., Watanabe, S. (2008). NOTCH3 Signaling Pathway Plays Crucial Roles in the Proliferation of ErbB2-Negative Human Breast Cancer Cells. Cancer Res. 68: 1881-1888 [Abstract] [Full Text]  
  • Katoh, M., Katoh, M. (2007). WNT Signaling Pathway and Stem Cell Signaling Network. Clin. Cancer Res. 13: 4042-4045 [Abstract] [Full Text]  
  • Wu, J., Bresnick, E. H. (2007). Glucocorticoid and Growth Factor Synergism Requirement for Notch4 Chromatin Domain Activation. Mol. Cell. Biol. 27: 2411-2422 [Abstract] [Full Text]  
  • Hu, C., Dievart, A., Lupien, M., Calvo, E., Tremblay, G., Jolicoeur, P. (2006). Overexpression of Activated Murine Notch1 and Notch3 in Transgenic Mice Blocks Mammary Gland Development and Induces Mammary Tumors. Am. J. Pathol. 168: 973-990 [Abstract] [Full Text]  
  • Stylianou, S., Clarke, R. B., Brennan, K. (2006). Aberrant Activation of Notch Signaling in Human Breast Cancer. Cancer Res. 66: 1517-1525 [Abstract] [Full Text]  
  • Reedijk, M., Odorcic, S., Chang, L., Zhang, H., Miller, N., McCready, D. R., Lockwood, G., Egan, S. E. (2005). High-level Coexpression of JAG1 and NOTCH1 Is Observed in Human Breast Cancer and Is Associated with Poor Overall Survival. Cancer Res. 65: 8530-8537 [Abstract] [Full Text]  
  • Nakakura, E. K., Sriuranpong, V. R., Kunnimalaiyaan, M., Hsiao, E. C., Schuebel, K. E., Borges, M. W., Jin, N., Collins, B. J., Nelkin, B. D., Chen, H., Ball, D. W. (2005). Regulation of Neuroendocrine Differentiation in Gastrointestinal Carcinoid Tumor Cells by Notch Signaling. J. Clin. Endocrinol. Metab. 90: 4350-4356 [Abstract] [Full Text]  
  • Cuevas, I. C., Slocum, A. L., Jun, P., Costello, J. F., Bollen, A. W., Riggins, G. J., McDermott, M. W., Lal, A. (2005). Meningioma Transcript Profiles Reveal Deregulated Notch Signaling Pathway. Cancer Res. 65: 5070-5075 [Abstract] [Full Text]  
  • Pece, S., Serresi, M., Santolini, E., Capra, M., Hulleman, E., Galimberti, V., Zurrida, S., Maisonneuve, P., Viale, G., Di Fiore, P. P. (2004). Loss of negative regulation by Numb over Notch is relevant to human breast carcinogenesis. JCB 167: 215-221 [Abstract] [Full Text]  
  • Vercauteren, S. M., Sutherland, H. J. (2004). Constitutively active Notch4 promotes early human hematopoietic progenitor cell maintenance while inhibiting differentiation and causes lymphoid abnormalities in vivo. Blood 104: 2315-2322 [Abstract] [Full Text]  
  • Das, I., Craig, C., Funahashi, Y., Jung, K.-M., Kim, T.-W., Byers, R., Weng, A. P., Kutok, J. L., Aster, J. C., Kitajewski, J. (2004). Notch Oncoproteins Depend on {gamma}-Secretase/Presenilin Activity for Processing and Function. J. Biol. Chem. 279: 30771-30780 [Abstract] [Full Text]  
  • Wang, X.-D., Shou, J., Wong, P., French, D. M., Gao, W.-Q. (2004). Notch1-expressing Cells Are Indispensable for Prostatic Branching Morphogenesis during Development and Re-growth Following Castration and Androgen Replacement. J. Biol. Chem. 279: 24733-24744 [Abstract] [Full Text]  
  • Tetzlaff, M. T., Yu, W., Li, M., Zhang, P., Finegold, M., Mahon, K., Harper, J. W., Schwartz, R. J., Elledge, S. J. (2004). Inaugural Article, From The Cover: Defective cardiovascular development and elevated cyclin E and Notch proteins in mice lacking the Fbw7 F-box protein. Proc. Natl. Acad. Sci. USA 101: 3338-3345 [Abstract] [Full Text]  
  • Weng, A. P., Nam, Y., Wolfe, M. S., Pear, W. S., Griffin, J. D., Blacklow, S. C., Aster, J. C. (2003). Growth Suppression of Pre-T Acute Lymphoblastic Leukemia Cells by Inhibition of Notch Signaling. Mol. Cell. Biol. 23: 655-664 [Abstract] [Full Text]  
  • Jeffries, S., Robbins, D. J., Capobianco, A. J. (2002). Characterization of a High-Molecular-Weight Notch Complex in the Nucleus of Notchic-Transformed RKE Cells and in a Human T-Cell Leukemia Cell Line. Mol. Cell. Biol. 22: 3927-3941 [Abstract] [Full Text]  
  • Sriuranpong, V., Borges, M. W., Strock, C. L., Nakakura, E. K., Watkins, D. N., Blaumueller, C. M., Nelkin, B. D., Ball, D. W. (2002). Notch Signaling Induces Rapid Degradation of Achaete-Scute Homolog 1. Mol. Cell. Biol. 22: 3129-3139 [Abstract] [Full Text]  
  • Hendrix, M. J. C., Seftor, R. E. B., Seftor, E. A., Gruman, L. M., Lee, L. M. L., Nickoloff, B. J., Miele, L., Sheriff, D. D., Schatteman, G. C. (2002). Transendothelial Function of Human Metastatic Melanoma Cells: Role of the Microenvironment in Cell-Fate Determination. Cancer Res. 62: 665-668 [Abstract] [Full Text]  
  • Orlandi, R., Cattaneo, M., Troglio, F., Casalini, P., Ronchini, C., Menard, S., Biunno, I. (2002). SEL1L Expression Decreases Breast Tumor Cell Aggressiveness in Vivo and in Vitro. Cancer Res. 62: 567-574 [Abstract] [Full Text]  
  • Wu, G., Lyapina, S., Das, I., Li, J., Gurney, M., Pauley, A., Chui, I., Deshaies, R. J., Kitajewski, J. (2001). SEL-10 Is an Inhibitor of Notch Signaling That Targets Notch for Ubiquitin-Mediated Protein Degradation. Mol. Cell. Biol. 21: 7403-7415 [Abstract] [Full Text]  
  • Xia, X., Qian, S., Soriano, S., Wu, Y., Fletcher, A. M., Wang, X.-J., Koo, E. H., Wu, X., Zheng, H. (2001). Loss of presenilin 1 is associated with enhanced beta -catenin signaling and skin tumorigenesis. Proc. Natl. Acad. Sci. USA 10.1073/pnas.191284198v1 [Abstract] [Full Text]  
  • Gordadze, A. V., Peng, R., Tan, J., Liu, G., Sutton, R., Kempkes, B., Bornkamm, G. W., Ling, P. D. (2001). Notch1IC Partially Replaces EBNA2 Function in B Cells Immortalized by Epstein-Barr Virus. J. Virol. 75: 5899-5912 [Abstract] [Full Text]  
  • Gridley, T. (2001). Notch signaling during vascular development. Proc. Natl. Acad. Sci. USA 98: 5377-5378 [Full Text]  
  • Ansieau, S., Strobl, L. J., Leutz, A. (2001). Activation of the Notch-regulated transcription factor CBF1/RBP-J{kappa} through the 13SE1A oncoprotein. Genes Dev. 15: 380-385 [Abstract] [Full Text]  
  • Jeffries, S., Capobianco, A. J. (2000). Neoplastic Transformation by Notch Requires Nuclear Localization. Mol. Cell. Biol. 20: 3928-3941 [Abstract] [Full Text]  
  • Krebs, L. T., Xue, Y., Norton, C. R., Shutter, J. R., Maguire, M., Sundberg, J. P., Gallahan, D., Closson, V., Kitajewski, J., Callahan, R., Smith, G. H., Stark, K. L., Gridley, T. (2000). Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 14: 1343-1352 [Abstract] [Full Text]  
  • Strobl, L. J., Höfelmayr, H., Marschall, G., Brielmeier, M., Bornkamm, G. W., Zimber-Strobl, U. (2000). Activated Notch1 Modulates Gene Expression in B Cells Similarly to Epstein-Barr Viral Nuclear Antigen 2. J. Virol. 74: 1727-1735 [Abstract] [Full Text]  
  • Hamada, Y, Kadokawa, Y, Okabe, M, Ikawa, M, Coleman, J., Tsujimoto, Y (1999). Mutation in ankyrin repeats of the mouse Notch2 gene induces early embryonic lethality. Development 126: 3415-3424 [Abstract]  
  • Halder, S. K., Takemori, H., Hatano, O., Nonaka, Y., Wada, A., Okamoto, M. (1998). Cloning of a Membrane-Spanning Protein with Epidermal Growth Factor-Like Repeat Motifs from Adrenal Glomerulosa Cells. Endocrinology 139: 3316-3328 [Abstract] [Full Text]  
  • Go, M., Eastman, D., Artavanis-Tsakonas, S (1998). Cell proliferation control by Notch signaling in Drosophila development. Development 125: 2031-2040 [Abstract]  
  • Hubbard, E. J. A., Wu, G., Kitajewski, J., Greenwald, I. (1997). sel-10, a negative regulator of lin-12 activity in Caenorhabditis elegans, encodes a member of the CDC4 family of proteins. Genes Dev. 11: 3182-3193 [Abstract] [Full Text]  
  • Garces, C., Ruiz-Hidalgo, M. J., de Mora, J. F., Park, C., Miele, L., Goldstein, J., Bonvini, E., Porras, A., Laborda, J. (1997). Notch-1 Controls the Expression of Fatty Acid-activated Transcription Factors and Is Required for Adipogenesis. J. Biol. Chem. 272: 29729-29734 [Abstract] [Full Text]  
  • Chen, H., Thiagalingam, A., Chopra, H., Borges, M. W., Feder, J. N., Nelkin, B. D., Baylin, S. B., Ball, D. W. (1997). Conservation of the Drosophila lateral inhibition pathway in human lung cancer: A hairy-related protein (HES-1) directly represses achaete-scute homolog-1 expression. Proc. Natl. Acad. Sci. USA 94: 5355-5360 [Abstract] [Full Text]  
  • Berry, L., Westlund, B, Schedl, T (1997). Germ-line tumor formation caused by activation of glp-1, a Caenorhabditis elegans member of the Notch family of receptors. Development 124: 925-936 [Abstract]  
  • Goode, S., Perrimon, N. (1997). Brainiac and Fringe Are Similar Pioneer Proteins That Impart Specificity to Notch Signaling during Drosophila Development. Cold Spring Harb Symp Quant Biol 62: 177-184 [Abstract]  
  • Milner, L. A., Bigas, A., Kopan, R., Brashem-Stein, C., Bernstein, I. D., Martin, D. I. K. (1996). Inhibition of granulocytic differentiation by mNotch1. Proc. Natl. Acad. Sci. USA 93: 13014-13019 [Abstract] [Full Text]  
  • Girard, L, Hanna, Z, Beaulieu, N, Hoemann, C D, Simard, C, Kozak, C A, Jolicoeur, P (1996). Frequent provirus insertional mutagenesis of Notch1 in thymomas of MMTVD/myc transgenic mice suggests a collaboration of c-myc and Notch1 for oncogenesis.. Genes Dev. 10: 1930-1944 [Abstract]  
  • Uyttendaele, H, Marazzi, G, Wu, G, Yan, Q, Sassoon, D, Kitajewski, J (1996). Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene. Development 122: 2251-2259 [Abstract]  
  • Fitzgerald, K, Greenwald, I (1995). Interchangeability of Caenorhabditis elegans DSL proteins and intrinsic signalling activity of their extracellular domains in vivo. Development 121: 4275-4282 [Abstract]  
  • Oka, C, Nakano, T, Wakeham, A, de la Pompa, J., Mori, C, Sakai, T, Okazaki, S, Kawaichi, M, Shiota, K, Mak, T., Honjo, T (1995). Disruption of the mouse RBP-J kappa gene results in early embryonic death. Development 121: 3291-3301 [Abstract]  
  • Nye, J. S., Kopan, R., Axel, R. (1994). An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells. Development 120: 2421-2430 [Abstract]  
  • Swiatek, P J, Lindsell, C E, del Amo, F F, Weinmaster, G, Gridley, T (1994). Notch1 is essential for postimplantation development in mice.. Genes Dev. 8: 707-719 [Abstract]  
  • Aster, J., Pear, W., Hasserjian, R., Erba, H., Davi, F., Luo, B., Scott, M., Baltimore, D., Sklar, J. (1994). Functional Analysis of the TAN-1 Gene, a Human Homolog of Drosophila Notch. Cold Spring Harb Symp Quant Biol 59: 125-136 [Abstract]  
  • Fitzgerald, K., Wilkinson, H. A., Greenwald, I. (1993). glp-1 can substitute for lin-12 in specifying cell fate decisions in Caenorhabditis elegans. Development 119: 1019-1027 [Abstract]  
  • Lieber, T, Kidd, S, Alcamo, E, Corbin, V, Young, M W (1993). Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei.. Genes Dev. 7: 1949-1965 [Abstract]  
  • Weinmaster, G., Roberts, V. J., Lemke, G. (1992). Notch2: a second mammalian Notch gene. Development 116: 931-941 [Abstract]  
  • Del Amo, F., Smith, D., Swiatek, P., Gendron-Maguire, M, Greenspan, R., McMahon, A., Gridley, T (1992). Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development. Development 115: 737-744 [Abstract]  
  • Kimble, J., Crittenden, S., Lambie, E., Kodoyianni, V., Mango, S., Troemel, E. (1992). Regulation of Induction by GLP1, a Localized Cell Surface Receptor in Caenorhabditis elegans. Cold Spring Harb Symp Quant Biol 57: 401-407 [Abstract]  
  • Xia, X., Qian, S., Soriano, S., Wu, Y., Fletcher, A. M., Wang, X.-J., Koo, E. H., Wu, X., Zheng, H. (2001). Loss of presenilin 1 is associated with enhanced beta -catenin signaling and skin tumorigenesis. Proc. Natl. Acad. Sci. USA 98: 10863-10868 [Abstract] [Full Text]