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The Homeodomain Protein Ladybird Late Regulates Synthesis of Milk Proteins during Pregnancy in the Tsetse Fly (Glossina morsitans).
- Source :
- PLoS Neglected Tropical Diseases; 4/24/2014, Vol. 8 Issue 4, p1-11, 11p
- Publication Year :
- 2014
-
Abstract
- Regulation of tissue and development specific gene expression patterns underlies the functional specialization of organs in multi-cellular organisms. In the viviparous tsetse fly (Glossina), the female accessory gland is specialized to generate nutrients in the form of a milk-like secretion to support growth of intrauterine larva. Multiple milk protein genes are expressed specifically in the female accessory gland and are tightly linked with larval development. Disruption of milk protein synthesis deprives developing larvae of nutrients and results in extended larval development and/or in abortion. The ability to cause such a disruption could be utilized as a tsetse control strategy. Here we identify and delineate the regulatory sequence of a major milk protein gene (milk gland protein 1:mgp1) by utilizing a combination of molecular techniques in tsetse, Drosophila transgenics, transcriptomics and in silico sequence analyses. The function of this promoter is conserved between tsetse and Drosophila. In transgenic Drosophila the mgp1 promoter directs reporter gene expression in a tissue and stage specific manner orthologous to that of Glossina. Analysis of the minimal required regulatory region of mgp1, and the regulatory regions of other Glossina milk proteins identified putative homeodomain protein binding sites as the sole common feature. Annotation and expression analysis of Glossina homeodomain proteins identified ladybird late (lbl) as being accessory gland/fat body specific and differentially expressed between lactating/non-lactating flies. Knockdown of lbl in tsetse resulted in a significant reduction in transcript abundance of multiple milk protein genes and in a significant loss of fecundity. The role of Lbl in adult reproductive physiology is previously unknown. These results suggest that Lbl is part of a conserved reproductive regulatory system that could have implications beyond tsetse to other vector insects such as mosquitoes. This system is critical for tsetse fecundity and provides a potential target for development of a reproductive inhibitor. Author Summary: Female tsetse flies (Diptera: Glossina) harbor and give birth to live young. To do this, they nourish their intrauterine larvae with milk secretions. This work focuses upon understanding the regulation of tsetse milk proteins, which are essential for fecundity and are expressed in a temporally and spatially specific manner by pregnant females. We identified the minimal upstream regulatory DNA sequence of the major milk protein gene mgp1, which confers tissue specific expression in the female accessory glands of reproductively active flies. This regulatory sequence functions similarly in transgenic fruit flies (Drosophila melanogaster) and drives expression of reporter gene products in the adult female accessory gland. Comparison of this regulatory sequence with sequences from other characterized milk proteins indicates that conserved homeodomain transcription factors may be responsible for regulating these genes. Analysis of Glossina homeodomain proteins identified an accessory gland/fat body specific factor, Ladybird late (lbl), which appears to regulate the expression of multiple milk proteins. Reduction of lbl levels interferes with milk protein gene expression, which in turn reduces Glossina fecundity. These results suggest that milk proteins in Glossina are regulated by a conserved regulatory system mediated in part by the homeodomain transcription factor lbl. Components of this system could provide a target for development of a tsetse reproductive inhibitor. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 19352727
- Volume :
- 8
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- PLoS Neglected Tropical Diseases
- Publication Type :
- Academic Journal
- Accession number :
- 174305693
- Full Text :
- https://doi.org/10.1371/journal.pntd.0002645