The University of Southampton
University of Southampton Institutional Repository

Immunolocalisation of the D-melanogaster Nramp homologue Malvolio to gut and Malpighian tubules provides evidence that Malvolio and Nramp2 are orthologous

Immunolocalisation of the D-melanogaster Nramp homologue Malvolio to gut and Malpighian tubules provides evidence that Malvolio and Nramp2 are orthologous
Immunolocalisation of the D-melanogaster Nramp homologue Malvolio to gut and Malpighian tubules provides evidence that Malvolio and Nramp2 are orthologous
Nramp (Slc11a1) genes in mammals are associated with the transport of iron and other divalent cations; Nramp1 in macrophages involved in the innate immune response against intracellular pathogens, and Nramp2 with duodenal iron uptake and the transferrin–transferrin-receptor pathway of iron assimilation. The Drosophila melanogaster Nramp-related gene is known as Malvolio. The localisation of Malvolio protein was inferred from the enhancer trap line initially used to isolate Malvolio in a screen for mutants with defects in taste perception. Here we describe the generation of a Malvolio-reactive polyclonal antibody and apply it to evaluate Malvolio localisation during stages of D. melanogaster development, and compare the results with the localisation of the enhancer trap line identified with beta-galactosidase. All immunolocalisation studies have been confirmed to be specific with Malvolio-blocking peptides. Our results demonstrated expression within Malpighian tubules, testis, brain, the amnioserosa of embryos, the larval and adult alimentary canal. Expression within the gut was of significant interest, as mammalian Nramp2 in the gut plays a primary role in the acquisition of dietary iron. We confirm expression within the central nervous system and in cells of the haematopoietic system. By immunohistochemistry we showed that expression within cells was either punctuate, diffuse cytoplasmic or plasma membrane associated, or both. The staining within the gut indicates a degree of conservation of components for iron acquisition between flies and mammals, suggesting that a comparable mechanism has been retained during evolution.
Nramp, divalent cation transport, Drosophila melanogaster, innate immunity, brain, haemocyte, Malpighian tubule, gut cell
0022-0949
1988-1995
Folwell, James L.
2744e089-bc3d-4a85-a53b-534ea4282966
Barton, C. Howard
5dfb4e1a-d559-4b58-9036-31de1e6c9ad8
Shepherd, David
11aa6858-d19c-4450-82ff-11dff9dcd9c4
Folwell, James L.
2744e089-bc3d-4a85-a53b-534ea4282966
Barton, C. Howard
5dfb4e1a-d559-4b58-9036-31de1e6c9ad8
Shepherd, David
11aa6858-d19c-4450-82ff-11dff9dcd9c4

Folwell, James L., Barton, C. Howard and Shepherd, David (2006) Immunolocalisation of the D-melanogaster Nramp homologue Malvolio to gut and Malpighian tubules provides evidence that Malvolio and Nramp2 are orthologous. Journal of Experimental Biology, 209 (10), 1988-1995. (doi:10.1242/jeb.02193).

Record type: Article

Abstract

Nramp (Slc11a1) genes in mammals are associated with the transport of iron and other divalent cations; Nramp1 in macrophages involved in the innate immune response against intracellular pathogens, and Nramp2 with duodenal iron uptake and the transferrin–transferrin-receptor pathway of iron assimilation. The Drosophila melanogaster Nramp-related gene is known as Malvolio. The localisation of Malvolio protein was inferred from the enhancer trap line initially used to isolate Malvolio in a screen for mutants with defects in taste perception. Here we describe the generation of a Malvolio-reactive polyclonal antibody and apply it to evaluate Malvolio localisation during stages of D. melanogaster development, and compare the results with the localisation of the enhancer trap line identified with beta-galactosidase. All immunolocalisation studies have been confirmed to be specific with Malvolio-blocking peptides. Our results demonstrated expression within Malpighian tubules, testis, brain, the amnioserosa of embryos, the larval and adult alimentary canal. Expression within the gut was of significant interest, as mammalian Nramp2 in the gut plays a primary role in the acquisition of dietary iron. We confirm expression within the central nervous system and in cells of the haematopoietic system. By immunohistochemistry we showed that expression within cells was either punctuate, diffuse cytoplasmic or plasma membrane associated, or both. The staining within the gut indicates a degree of conservation of components for iron acquisition between flies and mammals, suggesting that a comparable mechanism has been retained during evolution.

This record has no associated files available for download.

More information

Published date: 1 May 2006
Keywords: Nramp, divalent cation transport, Drosophila melanogaster, innate immunity, brain, haemocyte, Malpighian tubule, gut cell

Identifiers

Local EPrints ID: 56816
URI: http://eprints.soton.ac.uk/id/eprint/56816
ISSN: 0022-0949
PURE UUID: dba80c98-c50b-4700-ad2b-42dafbb24595
ORCID for David Shepherd: ORCID iD orcid.org/0000-0002-6961-7880

Catalogue record

Date deposited: 08 Aug 2008
Last modified: 06 Aug 2024 01:52

Export record

Altmetrics

Contributors

Author: James L. Folwell
Author: David Shepherd ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×