Boss/Sev Signaling from Germline to Soma Restricts Germline-Stem-Cell-Niche Formation in the Anterior Region of Drosophila Male Gonads

Developmental Cell

Volumn 13, Issue 1, 2007, Pages 151-159

  Kitadate, Yu ^a,b   Shigenobu, Shuji ^a,b   Arita, Kayo ^a   Kobayashi, Satoru ^a,b,c  

^a OKAZAKI INSTITUTE FOR INTEGRATIVE BIOSCIENCE   (Japan)

^b GRADUATE UNIVERSITY FOR ADVANCED STUDIES   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

DEVBIO; STEMCELL

Indexed keywords

BRIDE OF SEVENLESS PROTEIN; LIGAND; PROTEIN TYROSINE KINASE; SEVENLESS PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CONTROLLED STUDY; DROSOPHILA; EMBRYO; GERM LINE; GONAD DEVELOPMENT; MALE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEX DETERMINATION; SIGNAL TRANSDUCTION; SOMATIC CELL; STEM CELL; TESTIS;

ANIMALS; CELL ADHESION MOLECULES, NEURONAL; CELL DIFFERENTIATION; DROSOPHILA; DROSOPHILA PROTEINS; EYE PROTEINS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GERM CELLS; MALE; MEMBRANE GLYCOPROTEINS; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTORS, PEPTIDE; SIGNAL TRANSDUCTION; STEM CELLS; TESTIS;

EID: 34250845835     PISSN: 15345807     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.devcel.2007.05.001     Document Type: Article

References (46)

1. Alexson T.O., Hitoshi S., Coles B.L., Bernstein A., and van der Kooy D. Notch signaling is required to maintain all neural stem cell populations-irrespective of spatial or temporal niche. Dev. Neurosci. 28 (2006) 34-48
2. Basler K., Christen B., and Hafen E. Ligand-independent activation of the sevenless receptor tyrosine kinase changes the fate of cells in the developing Drosophila eye. Cell 64 (1991) 1069-1081
3. Biggs W.H., Zavitz K.H., Dickson B., Vanderstraten A., Brunner D., Hafen E., and Zipursky S.L. The Drosophila rolled locus encodes a MAP kinase required in the sevenless signal transduction pathway. EMBO J. 13 (1994) 1628-1635
4. Brand U., Fletcher J.C., Hobe M., Meyerowitz E.M., and Simon R. Dependence of stem cell fate in Arabidopsis on a feedback loop regulated by CLV3 activity. Science 289 (2000) 617-619
5. Brower D.L., Smith R.J., and Wilcox M. Differentiation within the gonads of Drosophila revealed by immunofluorescence. J. Embryol. Exp. Morphol. 63 (1981) 233-242
6. Burns C.E., Traver D., Mayhall E., Shepard J.L., and Zon L.I. Hematopoietic stem cell fate is established by the Notch-Runx pathway. Genes Dev. 19 (2005) 2331-2342
7. Calvi L.M., Adams G.B., Weibrecht K.W., Weber J.M., Olson D.P., Knight M.C., Martin R.P., Schipani E., Divieti P., Bringhurst F.R., et al. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature 425 (2003) 836-841
8. Campos L.S., Decker L., Taylor V., and Skarnes W. Notch, epidermal growth factor receptor, and β1-integrin pathways are coordinated in neural stem cells. J. Biol. Chem. 281 (2006) 5300-5309
9. Campos-Ortega J.A., and Hartenstein V. The Embryonic Development of Drosophila melanogaster. Second Edition (1997), Springer-Verlag, Berlin
10. DeFalco T.J., Verney G., Jenkins A.B., McCaffery J.M., Russell S., and Van Doren M. Sex-specific apoptosis regulates sexual dimorphism in the Drosophila embryonic gonad. Dev. Cell 5 (2003) 205-216
11. DeFalco T., Le Bras S., and Van Doren M. Abdominal-B is essential for proper sexually dimorphic development of the Drosophila gonad. Mech. Dev. 121 (2004) 1323-1333
12. Delorenzi M., and Bienz M. Expression of Abdominal-B homeoproteins in Drosophila embryos. Development 108 (1990) 323-329
13. Duncan I.W., and Kaufman T.C. Cytogenetic analysis of chromosome 3 in Drosophila melanogaster: mapping of the proximal portion of the right arm. Genetics 80 (1975) 733-752
14. Fre S., Huyghe M., Mourikis P., Robine S., Louvard D., and Artavanis-Tsakonas S. Notch signals control the fate of immature progenitor cells in the intestine. Nature 435 (2005) 964-968
15. Fuchs E., Tumbar T., and Guasch G. Socializing with the neighbors: stem cells and their niche. Cell 116 (2004) 769-778
16. Gilboa L., and Lehmann R. How different is Venus from Mars? The genetics of germ-line stem cells in Drosophila females and males. Development 131 (2004) 4895-4905
17. Gilboa L., and Lehmann R. Soma-germline interactions coordinate homeostasis and growth in the Drosophila gonad. Nature 443 (2006) 97-100
18. Gönczy P., and DiNardo S. The germ line regulates somatic cyst cell proliferation and fate during Drosophila spermatogenesis. Development 122 (1996) 2437-2447
19. Hafen E., Basler K., Edstroem J.E., and Rubin G.M. Sevenless, a cell-specific homeotic gene of Drosophila, encodes a putative transmembrane receptor with a tyrosine kinase domain. Science 236 (1987) 55-63
20. Hardy R.W., Tokuyasu K.T., Lindsley D.L., and Garavito M. The germinal proliferation center in the testis of Drosophila melanogaster. J. Ultrastruct. Res. 69 (1979) 180-190
21. Hart A.C., Krämer H., Van Vactor D.L., Paidhungat M., and Zipursky S.L. Induction of cell fate in the Drosophila retina: the bride of sevenless protein is predicted to contain a large extracellular domain and seven transmembrane segments. Genes Dev. 4 (1990) 1835-1847
22. Hayashi Y., Hayashi M., and Kobayashi S. Nanos suppresses somatic cell fate in Drosophila germ line. Proc. Natl. Acad. Sci. USA 101 (2004) 10338-10342
23. Kidd S., Baylies M.K., Gasic G.P., and Young M.W. Structure and distribution of the Notch protein in developing Drosophila. Genes Dev. 3 (1989) 1113-1129
24. Kiger A.A., Jones D.L., Schulz C., Rogers M.B., and Fuller M.T. Stem cell self-renewal specified by JAK-STAT activation in response to a support cell cue. Science 294 (2001) 2542-2545
25. Kobayashi S., Amikura R., Nakamura A., and Lasko P.F. Techniques for analyzing protein and RNA distribution in Drosophila ovaries and embryos at structural and ultrastructural resolution. In: Richter J. (Ed). A Comparative Methods Approach to the Study of Oocytes and Embryos (1999), Oxford University Press, New York 426-445
26. Le Bras S., and Van Doren M. Development of the male germline stem cell niche in Drosophila. Dev. Biol. 294 (2006) 92-103
27. Lehmann R., and Nüsslein-Volhard C. Abdominal segmentation, pole cell formation, and embryonic polarity require the localized activity of oskar, a maternal gene in Drosophila. Cell 47 (1986) 141-152
28. Luo D., Renault V.M., and Rando T.A. The regulation of Notch signaling in muscle stem cell activation and postnatal myogenesis. Semin. Cell Dev. Biol. 16 (2005) 612-622
29. Micchelli C.A., and Perrimon N. Evidence that stem cells reside in the adult Drosophila midgut epithelium. Nature 439 (2006) 475-479
30. Moore K.A., and Lemischka I.R. Stem cells and their niches. Science 311 (2006) 1880-1885
31. Mukai M., Kitadate Y., Arita K., Shigenobu S., and Kobayashi S. Expression of meiotic genes in the germline progenitors of Drosophila embryos. Gene Expr. Patterns 6 (2006) 256-266
32. Ohlstein B., and Spradling A. The adult Drosophila posterior midgut is maintained by pluripotent stem cells. Nature 439 (2006) 470-474
33. Ohlstein B., Kai T., Decotto E., and Spradling A. The stem cell niche: theme and variations. Curr. Opin. Cell Biol. 16 (2004) 693-699
34. Raabe T. The sevenless signaling pathway: variations of a common theme. Biochim. Biophys. Acta 1496 (2000) 151-163
35. Schoof H., Lenhard M., Haecker A., Mayer K.F.X., Jurgens G., and Laux T. The stem cell population of Arabidopsis shoot meristems is maintained by a regulatory loop between the CLAVATA and WUSCHEL genes. Cell 100 (2000) 635-644
36. Shigenobu S., Arita K., Kitadate Y., Noda C., and Kobayashi S. Isolation of germline cells from Drosophila embryos by flow cytometry. Dev. Growth Differ. 48 (2006) 49-57
37. Song X., Call G.B., Kirilly D., and Xie T. Notch signaling controls germline stem cell niche formation in the Drosophila ovary. Development 134 (2007) 1071-1080
38. Stanger B.Z., Datar R., Murtaugh L.C., and Melton D.A. Direct regulation of intestinal fate by Notch. Proc. Natl. Acad. Sci. USA 102 (2005) 12443-12448
39. Sundaram M.V. The love-hate relationship between Ras and Notch. Genes Dev. 19 (2005) 1825-1839
40. Tomlinson A., and Ready D.F. Sevenless: a cell-specific homeotic mutation of the Drosophila eye. Science 231 (1986) 400-402
41. Tulina N., and Matunis E. Control of stem cell self-renewal in Drosophila spermatogenesis by JAK-STAT signaling. Science 294 (2001) 2546-2549
42. Voas M.G., and Rebay I. Signal integration during development: insights from the Drosophila eye. Dev. Dyn. 229 (2004) 162-175
43. Ward E.J., Shcherbata H.R., Reynolds S.H., Fischer K.A., Hatfield S.D., and Ruohola-Baker H. Stem cells signal to the niche through the Notch pathway in the Drosophila ovary. Curr. Biol. 16 (2006) 2352-2358
44. Woodward W.A., Chen M.S., Behbod F., and Rosen J.M. On mammary stem cells. J. Cell Sci. 118 (2005) 3585-3594
45. Yamashita Y.M., Jones D.L., and Fuller M.T. Orientation of asymmetric stem cell division by the APC tumor suppressor and centrosome. Science 301 (2003) 1547-1550
46. Zhang J., Niu C., Ye L., Huang H., He X., Tong W.G., Ross J., Haug J., Johnson T., Feng J.Q., et al. Identification of the haematopoietic stem cell niche and control of the niche size. Nature 425 (2003) 836-841