» Articles » PMID: 18328473

Shape and Function of the Bicoid Morphogen Gradient in Dipteran Species with Different Sized Embryos

Overview
Journal Dev Biol
Publisher Elsevier
Date 2008 Mar 11
PMID 18328473
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

The Bicoid morphogen evolved approximately 150 MYA from a Hox3 duplication and is only found in higher dipterans. A major difference between dipteran species, however, is the size of the embryo, which varies up to 5-fold. Although the expression of developmental factors scale with egg length, it remains unknown how this scaling is achieved. To test whether scaling is accounted for by the properties of Bicoid, we expressed eGFP fused to the coding region of bicoid from three dipteran species in transgenic Drosophila embryos using the Drosophila bicoid cis-regulatory and mRNA localization sequences. In such embryos, we find that Lucilia sericata and Calliphora vicina Bicoid produce gradients very similar to the endogenous Drosophila gradient and much shorter than what they would have produced in their own respective species. The common shape of the Drosophila, Lucilia and Calliphora Bicoid gradients appears to be a conserved feature of the Bicoid protein. Surprisingly, despite their similar distributions, we find that Bicoid from Lucilia and Calliphora do not rescue Drosophila bicoid mutants, suggesting that that Bicoid proteins have evolved species-specific functional amino acid differences. We also found that maternal expression and anteriorly localization of proteins other than Bcd does not necessarily give rise to a gradient; eGFP produced a uniform protein distribution. However, a shallow gradient was observed using eGFP-NLS, suggesting nuclear localization may be necessary but not sufficient for gradient formation.

Citing Articles

Scale invariance in early embryonic development.

Nikolic M, Antonetti V, Liu F, Muhaxheri G, Petkova M, Scheeler M Proc Natl Acad Sci U S A. 2024; 121(46):e2403265121.

PMID: 39514304 PMC: 11572962. DOI: 10.1073/pnas.2403265121.


Long-range formation of the Bicoid gradient requires multiple dynamic modes that spatially vary across the embryo.

Athilingam T, Nelanuthala A, Breen C, Karedla N, Fritzsche M, Wohland T Development. 2024; 151(3).

PMID: 38345326 PMC: 10911119. DOI: 10.1242/dev.202128.


Scale invariance in early embryonic development.

Nikolic M, Antonetti V, Liu F, Muhaxheri G, Petkova M, Scheeler M ArXiv. 2024; .

PMID: 38235065 PMC: 10793483.


The impact of cell size on morphogen gradient precision.

Adelmann J, Vetter R, Iber D Development. 2023; 150(10).

PMID: 37249125 PMC: 10281552. DOI: 10.1242/dev.201702.


Patterning precision under non-linear morphogen decay and molecular noise.

Adelmann J, Vetter R, Iber D Elife. 2023; 12.

PMID: 37102505 PMC: 10139688. DOI: 10.7554/eLife.84757.


References
1.
Driever W, Nusslein-Volhard C . The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner. Cell. 1988; 54(1):95-104. DOI: 10.1016/0092-8674(88)90183-3. View

2.
Ruvinsky I, Ruvkun G . Functional tests of enhancer conservation between distantly related species. Development. 2003; 130(21):5133-42. DOI: 10.1242/dev.00711. View

3.
HAZELRIGG T, Liu N, Hong Y, Wang S . GFP expression in Drosophila tissues: time requirements for formation of a fluorescent product. Dev Biol. 1998; 199(2):245-9. DOI: 10.1006/dbio.1998.8922. View

4.
Driever W, Nusslein-Volhard C . The bicoid protein is a positive regulator of hunchback transcription in the early Drosophila embryo. Nature. 1989; 337(6203):138-43. DOI: 10.1038/337138a0. View

5.
Schroder R, Sander K . A comparison of transplantable bicoid activity and partial bicoid homeobox sequences in several Drosophila and blowfly species (Calliphoridae). Rouxs Arch Dev Biol. 2017; 203(1-2):34-43. DOI: 10.1007/BF00539888. View