The EGF-like homeotic protein dlk affects cell growth and interacts with growth-modulating molecules in the yeast two-hybrid system.

Levels of dlk, an EGF-like homeotic protein, are critical for several differentiation processes. Because growth and differentiation are, in general, exclusive of each other, and increasing evidence indicates that Dlk1 expression changes in tumorigenic processes, we studied whether dlk could also affect cell growth. We found that, in response to glucocorticoids, Balb/c 3T3 cells with diminished levels of dlk expression develop foci-like cells that have lost contact inhibition, display altered morphology, and grow faster than control cell lines. Balb/c 3T3 cells spontaneously growing more rapidly are also dlk-negative cells. Moreover, screening by the yeast two-hybrid system, using Dlk1 constructs as baits, resulted in the isolation of GAS1 and acrogranin cDNAs. Interestingly, these proteins are cysteine-rich molecules involved in the control of cell growth. Taken together, these observations suggest that dlk may participate in a network of interactions controlling how the cells respond to growth or differentiation signals.

[1]  V. Baladrón,et al.  dlk modulates mitogen-activated protein kinase signaling to allow or prevent differentiation. , 2002, Experimental cell research.

[2]  R. Kageyama,et al.  dlk Inhibits Stem Cell Factor‐Induced Colony Formation of Murine Hematopoietic Progenitors: Hes‐1‐Independent Effect , 2001, Stem cells.

[3]  K. Boon,et al.  SAGE analysis of neuroblastoma reveals a high expression of the human homologue of the Drosophila Delta gene. , 2000, Medical and pediatric oncology.

[4]  M. Yamazaki,et al.  Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3 , 2000, Genes to cells : devoted to molecular & cellular mechanisms.

[5]  S. Murphy,et al.  Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation. , 2000, Genome research.

[6]  M. E. Ruaro,et al.  Analysis of the domain requirement in Gas1 growth suppressing activity , 2000, FEBS letters.

[7]  M. E. Ruaro,et al.  The growth suppressing gas1 product is a GPI‐linked protein , 2000, FEBS letters.

[8]  S. Tilghman,et al.  The Dlk1 and Gtl2 genes are linked and reciprocally imprinted. , 2000, Genes & development.

[9]  V. Baladrón,et al.  Assignment of dlk (Dlk1) to mouse chromosome band 12E–F1 by in situ hybridization , 2000, Cytogenetic and Genome Research.

[10]  G. Serrero,et al.  Inhibition of PC cell-derived growth factor (PCDGF, epithelin/granulin precursor) expression by antisense PCDGF cDNA transfection inhibits tumorigenicity of the human breast carcinoma cell line MDA-MB-468. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[11]  H. Nakauchi,et al.  A Role for Pref-1 and HES-1 in Thymocyte Development , 2000, The Journal of Immunology.

[12]  J. Laborda,et al.  The role of the epidermal growth factor-like protein dlk in cell differentiation. , 2000, Histology and histopathology.

[13]  V. Baladrón,et al.  Assignment1 of DLK1 to human chromosome band 14q32 by in situ hybridization , 1999, Cytogenetic and Genome Research.

[14]  J. Laborda,et al.  Adipocyte differentiation is modulated by secreted delta-like (dlk) variants and requires the expression of membrane-associated dlk. , 1999, Differentiation; research in biological diversity.

[15]  R. J. Fleming,et al.  Structural conservation of Notch receptors and ligands. , 1998, Seminars in cell & developmental biology.

[16]  H. Sul,et al.  Transcriptional Control of the pref-1 Gene in 3T3-L1 Adipocyte Differentiation , 1998, The Journal of Biological Chemistry.

[17]  U. Lendahl,et al.  Notch and neurogenesis , 1998, Journal of neuroscience research.

[18]  S. Bauer,et al.  Modulated Expression of the Epidermal Growth Factor-Like Homeotic Protein dlk Influences Stromal-Cell–Pre-B-Cell Interactions, Stromal Cell Adipogenesis, and Pre-B-Cell Interleukin-7 Requirements , 1998, Molecular and Cellular Biology.

[19]  A. Bateman,et al.  Granulins: the structure and function of an emerging family of growth factors. , 1998, The Journal of endocrinology.

[20]  M. Okamoto,et al.  Cloning of a membrane-spanning protein with epidermal growth factor-like repeat motifs from adrenal glomerulosa cells. , 1998, Endocrinology.

[21]  A. Evdokiou,et al.  Growth-regulatory activity of the growth arrest-specific gene, GAS1, in NIH3T3 fibroblasts. , 1998, Experimental cell research.

[22]  X. Xia,et al.  Identification of cell surface binding sites for PC-cell-derived growth factor, PCDGF, (epithelin/granulin precursor) on epithelial cells and fibroblasts. , 1998, Biochemical and biophysical research communications.

[23]  A. Evdokiou,et al.  Tumor‐suppressive activity of the growth arrest‐specific gene GAS1 in human tumor cell lines , 1998, International journal of cancer.

[24]  N. Watanabe,et al.  Positive and negative thymocyte selection. , 1998, Critical reviews in immunology.

[25]  D. Spandidos,et al.  Expression of ras proto-oncogenes: regulation and implications in the development of human tumors. , 1997, Critical reviews in oncology/hematology.

[26]  A. Levine,et al.  A proline-rich motif in p53 is required for transactivation-independent growth arrest as induced by Gas1. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[27]  Cleavage of membrane-associated pref-1 generates a soluble inhibitor of adipocyte differentiation. , 1997, Molecular and cellular biology.

[28]  E. Craig,et al.  Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. , 1996, Genetics.

[29]  D. Spandidos,et al.  The association of the H-ras oncogene and steroid hormone receptors in gynecological cancer. , 1996, Journal of experimental therapeutics & oncology.

[30]  D. Spandidos,et al.  Glucocorticoid and Estrogen Receptors Have Elevated Activity in Human Endometrial and Ovarian Tumors as Compared to the Adjacent Normal Tissues and Recognize Sequence Elements of the H‐ras Proto‐oncogene , 1996, Japanese journal of cancer research : Gann.

[31]  P. Gruppuso,et al.  Regulation of preadipocyte factor-1 gene expression during 3T3-L1 cell differentiation. , 1996, Endocrinology.

[32]  H. Sul,et al.  Characterization of Pref-1 and its inhibitory role in adipocyte differentiation. , 1996, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.

[33]  A. Levine,et al.  Gas1-induced growth suppression requires a transactivation-independent p53 function , 1995, Molecular and cellular biology.

[34]  R. Umek,et al.  Differential expression of gas and gadd genes at distinct growth arrest points during adipocyte development. , 1995, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[35]  L. Helman,et al.  dlk, pG2 and Pref-1 mRNAs encode similar proteins belonging to the EGF-like superfamily. Identification of polymorphic variants of this RNA. , 1995, Biochimica et biophysica acta.

[36]  O. MacDougald,et al.  Transcriptional regulation of gene expression during adipocyte differentiation. , 1995, Annual review of biochemistry.

[37]  H. Sul,et al.  Structural characterization and alternate splicing of the gene encoding the preadipocyte EGF-like protein pref-1. , 1994, Biochemistry.

[38]  M. E. Ruaro,et al.  Structure, function, and chromosome mapping of the growth-suppressing human homologue of the murine gas1 gene. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[39]  S. Fields The Two-Hybrid System to Detect Protein-Protein Interactions , 1993 .

[40]  H. Sul,et al.  Pref-1, a protein containing EGF-like repeats, inhibits adipocyte differentiation , 1993, Cell.

[41]  S. Elledge,et al.  The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit. , 1993, Genes & development.

[42]  G. Gerton,et al.  Acrogranin, an acrosomal cysteine‐rich glycoprotein, is the precursor of the growth‐modulating peptides, granulins, and epithelins, and is expressed in somatic as well as male germ cells , 1993, Molecular reproduction and development.

[43]  E. Sausville,et al.  dlk, a putative mammalian homeotic gene differentially expressed in small cell lung carcinoma and neuroendocrine tumor cell line. , 1993, The Journal of biological chemistry.

[44]  M. E. Ruaro,et al.  The growth arrest-specific gene, gas1, is involved in growth suppression , 1992, Cell.

[45]  K. Matsumoto,et al.  In vitro activation of distinct molecular and cellular phenotypes after induction of differentiation in a human neuroblastoma cell line. , 1992, Cancer research.

[46]  Y. Kassir,et al.  A simple and highly efficient procedure for rescuing autonomous plasmids from yeast. , 1992, Nucleic acids research.

[47]  R. J. Fleming,et al.  Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor , 1991, Cell.

[48]  M. Israel,et al.  Human neuroblastoma tumor cell lines correspond to the arrested differentiation of chromaffin adrenal medullary neuroblasts. , 1990, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[49]  F. Hoffmann,et al.  Homologs of vertebrate growth factors in Drosophila melanogaster and other invertebrates. , 1990, Current topics in developmental biology.

[50]  J. Engel EGF‐like domains in extracellular matrix proteins: Localized signals for growth and differentiation? , 1989, FEBS letters.

[51]  E Ruoslahti,et al.  New perspectives in cell adhesion: RGD and integrins. , 1987, Science.

[52]  L. Kopelovich,et al.  Kinetic analysis of hydrocortisone effect on the neodifferentiation of Kirsten murine sarcoma virus-transformed human skin fibroblasts to adipose cells. , 1987, Cancer investigation.

[53]  G. Carpenter,et al.  Epidermal growth factor, its receptor, and related proteins. , 1986, Experimental cell research.

[54]  L. Kopelovich,et al.  Hydrocortisone promotes the neodifferentiation of Kirsten murine sarcoma virus transformed human skin fibroblasts to adipose cells: relevance to oncogenic mechanisms. , 1986, Experimental cell biology.

[55]  O. Rosen,et al.  Organelle relationships in cultured 3T3-L1 preadipocytes , 1980, The Journal of cell biology.