A temperature-sensitive brain tumor suppressor mutation of Drosophila melanogaster: developmental studies and molecular localization of the gene
- PMID: 8507589
- DOI: 10.1016/0925-4773(93)90052-y
A temperature-sensitive brain tumor suppressor mutation of Drosophila melanogaster: developmental studies and molecular localization of the gene
Abstract
The recessive-lethal, temperature-sensitive (ts) mutation of the tumor suppressor gene lethal(3)malignant brain tumor (l(3)mbt) causes in a single step the malignant transformation of the adult optic neuroblasts and ganglion mother cells in the larval brain at the restrictive temperature of 29 degrees C. The transformed cells are differentiation-incompetent and grow autonomously in a lethal and invasive fashion in situ in the brain as well as after transplantation in vivo into wild-type adult hosts. The imaginal discs show epithelial overgrowth. At the permissive temperature of 22 degrees C development is completely normal. The ts-period of gene activity responsible for 100% brain tumor suppression and normal imaginal disc development encompasses the first six hours of embryonic development. The l(3)mbt gene function is, however, also required thereafter for the proper differentiation of the brain and the imaginal discs. The l(3)mbt gene is located cytologically in the salivary gland chromosome bands 97E8-F11, and in molecular terms in 29 kb of DNA detected via a P-element insertional deletion.
Similar articles
-
The Drosophila melanogaster tumor suppressor gene lethal(3)malignant brain tumor encodes a proline-rich protein with a novel zinc finger.Mech Dev. 1995 Sep;53(1):141-54. doi: 10.1016/0925-4773(95)00431-9. Mech Dev. 1995. PMID: 8555106
-
Genetic, cytogenetic and developmental analysis of the Drosophila melanogaster tumor suppressor gene lethal(2)tumorous imaginal discs (1(2)tid).Differentiation. 1992 Oct;51(2):91-104. doi: 10.1111/j.1432-0436.1992.tb00685.x. Differentiation. 1992. PMID: 1473626
-
A human homolog of Drosophila lethal(3)malignant brain tumor (l(3)mbt) protein associates with condensed mitotic chromosomes.Oncogene. 1999 Jul 1;18(26):3799-809. doi: 10.1038/sj.onc.1202732. Oncogene. 1999. PMID: 10445843
-
Drosophila as a model system for molecular analysis of tumorigenesis.Environ Health Perspect. 1991 Jun;93:63-71. doi: 10.1289/ehp.919363. Environ Health Perspect. 1991. PMID: 1773803 Free PMC article. Review.
-
Drosophila differentiation genes instrumental in tumor suppression.Int J Dev Biol. 1996 Feb;40(1):149-56. Int J Dev Biol. 1996. PMID: 8735924 Review.
Cited by
-
Stromal barriers and strategies for the delivery of nanomedicine to desmoplastic tumors.J Control Release. 2015 Dec 10;219:192-204. doi: 10.1016/j.jconrel.2015.08.017. Epub 2015 Aug 12. J Control Release. 2015. PMID: 26277065 Free PMC article. Review.
-
Functional interactions between the Moses corepressor and DHR78 nuclear receptor regulate growth in Drosophila.Genes Dev. 2007 Feb 15;21(4):450-64. doi: 10.1101/gad.1519007. Genes Dev. 2007. PMID: 17322404 Free PMC article.
-
l(3)malignant brain tumor and three novel genes are required for Drosophila germ-cell formation.Genetics. 2003 Dec;165(4):1889-900. doi: 10.1093/genetics/165.4.1889. Genetics. 2003. PMID: 14704174 Free PMC article.
-
An unregulated regulator: Vasa expression in the development of somatic cells and in tumorigenesis.Dev Biol. 2016 Jul 1;415(1):24-32. doi: 10.1016/j.ydbio.2016.05.012. Epub 2016 May 11. Dev Biol. 2016. PMID: 27179696 Free PMC article. Review.
-
Mercury chloride exposure induces DNA damage, reduces fertility, and alters somatic and germline cells in Drosophila melanogaster ovaries.Environ Sci Pollut Res Int. 2019 Nov;26(31):32322-32332. doi: 10.1007/s11356-019-06449-4. Epub 2019 Oct 9. Environ Sci Pollut Res Int. 2019. PMID: 31598926
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Miscellaneous