The elimination of an adult segment by the Hox gene Abdominal-B
- PMID: 26259679
- DOI: 10.1016/j.mod.2015.08.002
The elimination of an adult segment by the Hox gene Abdominal-B
Abstract
Hox gene activity leads to morphological diversity of organs or structures in different species. One special case of Hox function is the elimination of a particular structure. The Abdominal-B Hox gene of Drosophila melanogaster provides an example of such activity, as this gene suppresses the formation of the seventh abdominal segment in the adult. This elimination occurs only in males, and is characteristic of more advanced Diptera. The elimination requires the differential expression or activity of genes that are downstream Abdominal-B, or that work together with it, and which regulate cell proliferation or cell extrusion. Here, we review the mechanisms responsible for such elimination and provide some new data on processes taking place within this segment.
Keywords: Abdomen; Abdominal-B; Drosophila; Hox genes.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.
Similar articles
-
The lines gene of Drosophila is required for specific functions of the Abdominal-B HOX protein.Development. 1998 Apr;125(7):1269-74. doi: 10.1242/dev.125.7.1269. Development. 1998. PMID: 9477325
-
Hox-mediated regulation of doublesex sculpts sex-specific abdomen morphology in Drosophila.Dev Dyn. 2012 Jun;241(6):1076-90. doi: 10.1002/dvdy.23791. Epub 2012 Apr 26. Dev Dyn. 2012. PMID: 22488883
-
Direct integration of Hox and segmentation gene inputs during Drosophila development.Nature. 2004 Oct 7;431(7009):653-9. doi: 10.1038/nature02946. Nature. 2004. PMID: 15470419
-
Cellular analysis of newly identified Hox downstream genes in Drosophila.Eur J Cell Biol. 2010 Feb-Mar;89(2-3):273-8. doi: 10.1016/j.ejcb.2009.11.012. Epub 2009 Dec 16. Eur J Cell Biol. 2010. PMID: 20018403 Review.
-
Beyond homeosis--HOX function in morphogenesis and organogenesis.Differentiation. 2003 Oct;71(8):461-76. doi: 10.1046/j.1432-0436.2003.7108004.x. Differentiation. 2003. PMID: 14641327 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases