A CONSERVED SIGNALING PATHWAY: The Drosophila Toll-Dorsal Pathway

Annual Review of Cell and Developmental Biology - Tập 12 Số 1 - Trang 393-416 - 1996
Marcia Belvin1, Kathryn V. Anderson1
1Genetics Division, Department of Molecular and Cell Biology, University of California, Berkeley, California 94720

Tóm tắt

▪ Abstract  The Toll-Dorsal pathway in Drosophila and the interleukin-1 receptor (IL-1R)-NF-κB pathway in mammals are homologous signal transduction pathways that mediate several different biological responses. In Drosophila, genetic analysis of dorsal-ventral patterning of the embryo has defined the series of genes that mediate the Toll-Dorsal pathway. Binding of extracellular ligand activates the transmembrane receptor Toll, which requires the novel protein Tube to activate the cytoplasmic serine/threonine kinase Pelle. Pelle activity controls the degradation of the Cactus protein, which is present in a cytoplasmic complex with the Dorsal protein. Once Cactus is degraded in response to signal, Dorsal is free to move into the nucleus where it regulates transcription of specific target genes. The Toll, tube, pelle, cactus, and dorsal genes also appear to be involved in Drosophila immune response. Because the IL-1R-NF-κB pathway plays a role in vertebrate innate immunity and because plant homologues of the Toll-Dorsal pathway are important in plant disease resistance, it is likely that this pathway arose before the divergence of plants and animals as a defense against pathogens.

Từ khóa


Tài liệu tham khảo

10.1128/MCB.15.3.1294

10.1016/0092-8674(85)90274-0

10.1038/311223a0

Anderson KV, Nüsslein-Volhard C. 1986. Dorsal-group genes of Drosophila. InGametogenesis and the Early Embryo, ed. J Gall, pp. 177–94. New York: Liss

Åsling B, 1995, 36th Annu. Drosophila Res. Conf.

10.1016/0092-8674(88)90382-0

10.1128/MCB.13.6.3301

10.1101/gad.9.22.2736

10.1038/376167a0

10.1101/gad.9.7.783

Betts JC, 1993, J. Biol. Chem., 268, 25624, 10.1016/S0021-9258(19)74435-4

10.1126/science.7878466

10.1126/science.271.5252.1128

10.1101/gad.9.13.1586

Ciechanover A, 1994, Biol. Chem. Hoppe-Seyler, 375, 565

10.1042/bj3000567

10.1074/jbc.270.28.16514

10.1128/MCB.15.3.1302

10.1006/jmbi.1993.1392

Fey GH, Gauldie J. 1990. InProgress in Liver Disease, ed. H Topper, F Schaffner, pp. 89–116. Philadelphia: Saunders

Galindo RL, 1995, Development, 121, 2209, 10.1242/dev.121.7.2209

10.1091/mbc.3.12.1339

10.1016/0092-8674(92)90595-4

Gerttula S, 1988, Genetics, 119, 123, 10.1093/genetics/119.1.123

10.1128/MCB.14.6.3559

10.1016/B978-0-08-030804-3.50017-0

10.1128/MCB.16.3.1103

10.1038/372563a0

10.1006/dbio.1995.1134

Hashimoto C, 1991, Development, 111, 1021, 10.1242/dev.111.4.1021

10.1016/0092-8674(88)90516-8

10.1016/0092-8674(91)90022-Q

10.1002/j.1460-2075.1993.tb05939.x

Hecht PM, 1993, Genetics, 135, 405, 10.1093/genetics/135.2.405

Heguy A, 1992, J. Biol. Chem., 267, 2605, 10.1016/S0021-9258(18)45924-8

10.1038/365182a0

10.1016/0092-8674(92)90083-O

10.1016/0952-7915(95)80022-0

10.1016/0168-9525(93)90165-E

10.1016/0092-8674(91)90651-E

10.1016/0959-437X(94)90133-N

10.1101/gad.6.9.1728

10.1101/gad.6.8.1518

10.1016/0092-8674(93)90495-C

10.1073/pnas.91.12.5350

10.1101/gad.6.4.619

10.1128/MCB.15.4.2166

10.1016/0092-8674(93)90402-C

10.1002/j.1460-2075.1992.tb05387.x

10.1126/science.7973631

10.1002/j.1460-2075.1993.tb05800.x

10.1002/j.1460-2075.1990.tb07878.x

10.1016/0092-8674(92)90596-5

Koj A. 1985. Liver response to inflammation and synthesis of acute-phase plasma proteins. InThe Acute-Phase Response to Injury and Infection. Research Monographs in Cell and Tissue Physiology, ed. AH Gordon, A Koj, pp. 139–246. Amsterdam: Elsevier

10.1016/S0065-2776(08)60618-5

10.1073/pnas.89.17.8145

10.1073/pnas.92.22.10242

10.1038/371175a0

10.1002/j.1460-2075.1995.tb07029.x

10.1073/pnas.88.3.810

10.1002/j.1460-2075.1993.tb06019.x

10.1073/pnas.92.2.552

10.1016/0012-1606(79)90065-4

10.1126/science.7902614

10.1105/tpc.6.11.1543

10.1002/eji.1830240717

10.1073/pnas.90.21.10193

10.1073/pnas.91.26.12740

10.1016/S0065-230X(08)60257-2

10.1016/0092-8674(94)90507-X

10.1146/annurev.genet.29.1.371

10.1016/0014-5793(95)00541-G

10.1101/gad.6.9.1654

10.1016/0092-8674(92)90426-D

10.1101/gad.5.10.1892

10.1016/0968-0004(94)90115-5

10.1002/j.1460-2075.1995.tb07317.x

Rechsteiner M, 1990, Semin. Cell Biol., 1, 433

Reichhart JM, 1993, CR Acad. Sci. III, 316, 1218

10.1002/j.1460-2075.1992.tb05191.x

10.1128/MCB.15.5.2413

10.1126/science.2876518

Roth S, 1991, Development, 112, 371, 10.1242/dev.112.2.371

10.1016/0092-8674(89)90774-5

10.1016/0092-8674(89)90772-1

10.1073/pnas.90.19.8842

10.1073/pnas.92.24.11259

10.1101/gad.5.5.797

Schneider DS, 1994, Development, 120, 1243, 10.1242/dev.120.5.1243

10.1128/MCB.15.7.3960

10.1016/0092-8674(95)90415-8

10.1016/0092-8674(93)90071-W

10.1146/annurev.cb.10.110194.002201

Sipe JD. 1985. Cellular and humoral components of the early inflammatory reaction. InThe Acute-Phase Response to Injury and Infection. Research Monographs in Cell and Tissue Physiology, ed. AH Gordon, A Koj, pp. 3–21. Amsterdam: Elsevier

10.1126/science.270.5243.1804

10.1126/science.7732374

10.1126/science.3118464

10.1016/0092-8674(89)90773-3

Sun SC, 1991, J. Biol. Chem., 266, 6644, 10.1016/S0021-9258(18)38165-1

10.1128/MCB.15.7.3627

10.1016/0092-8674(91)90014-P

10.1002/j.1460-2075.1994.tb06878.x

10.1016/0092-8674(95)90416-6

10.1083/jcb.123.3.523

10.1016/0092-8674(94)90283-6

10.1016/0092-8674(95)90208-2