Drosophila laminin: sequence of B2 subunit and expression of all three subunits during embryogenesis (original) (raw)
Abstract
In a previous study, we described the cloning of the genes encoding the three subunits of Drosophila laminin, a substrate adhesion molecule, and the cDNA sequence of the B1 subunit (Montell and Goodman, 1988). This analysis revealed the similarity of Drosophila laminin with the mouse and human complexes in subunit composition, domain structure, and amino acid sequence. In this paper, we report the deduced amino acid sequence of the B2 subunit. We then describe the expression and tissue distribution of the three subunits of laminin during Drosophila embryogenesis using both in situ hybridization and immunolocalization techniques, with particular emphasis on its expression in and around the developing nervous system.
Full Text
The Full Text of this article is available as a PDF (3.2 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Akam M. E. The location of Ultrabithorax transcripts in Drosophila tissue sections. EMBO J. 1983;2(11):2075–2084. doi: 10.1002/j.1460-2075.1983.tb01703.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ball E. E., Ho R. K., Goodman C. S. Development of neuromuscular specificity in the grasshopper embryo: guidance of motoneuron growth cones by muscle pioneers. J Neurosci. 1985 Jul;5(7):1808–1819. doi: 10.1523/JNEUROSCI.05-07-01808.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chi H. C., Hui C. F. Primary structure of the Drosophila laminin B2 chain and comparison with human, mouse, and Drosophila laminin B1 and B2 chains. J Biol Chem. 1989 Jan 25;264(3):1543–1550. [PubMed] [Google Scholar]
- Chi H. C., Hui C. F. cDNA and amino acid sequences of Drosophila laminin B2 chain. Nucleic Acids Res. 1988 Jul 25;16(14B):7205–7206. doi: 10.1093/nar/16.14.7205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chiu A. Y., Matthew W. D., Patterson P. H. A monoclonal antibody that blocks the activity of a neurite regeneration-promoting factor: studies on the binding site and its localization in vivo. J Cell Biol. 1986 Oct;103(4):1383–1398. doi: 10.1083/jcb.103.4.1383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crews S. T., Thomas J. B., Goodman C. S. The Drosophila single-minded gene encodes a nuclear protein with sequence similarity to the per gene product. Cell. 1988 Jan 15;52(1):143–151. doi: 10.1016/0092-8674(88)90538-7. [DOI] [PubMed] [Google Scholar]
- Edgar D., Timpl R., Thoenen H. The heparin-binding domain of laminin is responsible for its effects on neurite outgrowth and neuronal survival. EMBO J. 1984 Jul;3(7):1463–1468. doi: 10.1002/j.1460-2075.1984.tb01997.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
- Fessler L. I., Campbell A. G., Duncan K. G., Fessler J. H. Drosophila laminin: characterization and localization. J Cell Biol. 1987 Nov;105(5):2383–2391. doi: 10.1083/jcb.105.5.2383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ho R. K., Ball E. E., Goodman C. S. Muscle pioneers: large mesodermal cells that erect a scaffold for developing muscles and motoneurones in grasshopper embryos. Nature. 1983 Jan 6;301(5895):66–69. doi: 10.1038/301066a0. [DOI] [PubMed] [Google Scholar]
- Jacobs J. R., Goodman C. S. Embryonic development of axon pathways in the Drosophila CNS. I. A glial scaffold appears before the first growth cones. J Neurosci. 1989 Jul;9(7):2402–2411. doi: 10.1523/JNEUROSCI.09-07-02402.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobs J. R., Goodman C. S. Embryonic development of axon pathways in the Drosophila CNS. II. Behavior of pioneer growth cones. J Neurosci. 1989 Jul;9(7):2412–2422. doi: 10.1523/JNEUROSCI.09-07-02412.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobs J. R., Hiromi Y., Patel N. H., Goodman C. S. Lineage, migration, and morphogenesis of longitudinal glia in the Drosophila CNS as revealed by a molecular lineage marker. Neuron. 1989 Jun;2(6):1625–1631. doi: 10.1016/0896-6273(89)90051-2. [DOI] [PubMed] [Google Scholar]
- Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature. 1975 Aug 7;256(5517):495–497. doi: 10.1038/256495a0. [DOI] [PubMed] [Google Scholar]
- Lander A. D., Fujii D. K., Reichardt L. F. Purification of a factor that promotes neurite outgrowth: isolation of laminin and associated molecules. J Cell Biol. 1985 Sep;101(3):898–913. doi: 10.1083/jcb.101.3.898. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Letourneau P. C., Madsen A. M., Palm S. L., Furcht L. T. Immunoreactivity for laminin in the developing ventral longitudinal pathway of the brain. Dev Biol. 1988 Jan;125(1):135–144. doi: 10.1016/0012-1606(88)90066-8. [DOI] [PubMed] [Google Scholar]
- Liesi P. Do neurons in the vertebrate CNS migrate on laminin? EMBO J. 1985 May;4(5):1163–1170. doi: 10.1002/j.1460-2075.1985.tb03755.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mirre C., Cecchini J. P., Le Parco Y., Knibiehler B. De novo expression of a type IV collagen gene in Drosophila embryos is restricted to mesodermal derivatives and occurs at germ band shortening. Development. 1988 Feb;102(2):369–376. doi: 10.1242/dev.102.2.369. [DOI] [PubMed] [Google Scholar]
- Mitchison T. J., Sedat J. Localization of antigenic determinants in whole Drosophila embryos. Dev Biol. 1983 Sep;99(1):261–264. doi: 10.1016/0012-1606(83)90275-0. [DOI] [PubMed] [Google Scholar]
- Montell D. J., Goodman C. S. Drosophila substrate adhesion molecule: sequence of laminin B1 chain reveals domains of homology with mouse. Cell. 1988 May 6;53(3):463–473. doi: 10.1016/0092-8674(88)90166-3. [DOI] [PubMed] [Google Scholar]
- Patel N. H., Snow P. M., Goodman C. S. Characterization and cloning of fasciclin III: a glycoprotein expressed on a subset of neurons and axon pathways in Drosophila. Cell. 1987 Mar 27;48(6):975–988. doi: 10.1016/0092-8674(87)90706-9. [DOI] [PubMed] [Google Scholar]
- Pikkarainen T., Kallunki T., Tryggvason K. Human laminin B2 chain. Comparison of the complete amino acid sequence with the B1 chain reveals variability in sequence homology between different structural domains. J Biol Chem. 1988 May 15;263(14):6751–6758. [PubMed] [Google Scholar]
- Rogers S. L., Edson K. J., Letourneau P. C., McLoon S. C. Distribution of laminin in the developing peripheral nervous system of the chick. Dev Biol. 1986 Feb;113(2):429–435. doi: 10.1016/0012-1606(86)90177-6. [DOI] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sasaki M., Kato S., Kohno K., Martin G. R., Yamada Y. Sequence of the cDNA encoding the laminin B1 chain reveals a multidomain protein containing cysteine-rich repeats. Proc Natl Acad Sci U S A. 1987 Feb;84(4):935–939. doi: 10.1073/pnas.84.4.935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sasaki M., Kleinman H. K., Huber H., Deutzmann R., Yamada Y. Laminin, a multidomain protein. The A chain has a unique globular domain and homology with the basement membrane proteoglycan and the laminin B chains. J Biol Chem. 1988 Nov 15;263(32):16536–16544. [PubMed] [Google Scholar]
- Sasaki M., Yamada Y. The laminin B2 chain has a multidomain structure homologous to the B1 chain. J Biol Chem. 1987 Dec 15;262(35):17111–17117. [PubMed] [Google Scholar]
- Thomas J. B., Crews S. T., Goodman C. S. Molecular genetics of the single-minded locus: a gene involved in the development of the Drosophila nervous system. Cell. 1988 Jan 15;52(1):133–141. doi: 10.1016/0092-8674(88)90537-5. [DOI] [PubMed] [Google Scholar]