Larval optic neuropils inChaoborus Further arguments for homology between Bolwig's organ and stemmata of primitive dipterans

Bolwig's organ is the larval light-sensing system consisting of 12 photoreceptors and its development requires atonal activity. Here, we showed that Bolwig's organ formation and atonal expression are controlled by the concerted function of hedgehog, eyes absent and sine oculis. Bolwig's organ primordium was first detected as a cluster of about 14 Atonal-positive cells at the posterior edge of the ocular segment in embryos and hence, atonal expression may define the region from which a few Atonal-positive founder cells (future primary photoreceptor cells) are generated by lateral specification. In Bolwig's organ development, neural differentiation precedes photoreceptor specification, since Elav, a neuron-specific antigen, whose expression is under the control of atonal, is expressed in virtually all early-Atonal-positive cells prior to the establishment of founder cells. Neither Atonal expression nor Bolwig's organ formation occurred in the absence of hedgehog, eyes absent or sine oculis activity. Genetic and histochemical analyses indicated that (1) responsible Hedgehog signals derive from the ocular segment, (2) Eyes absent and Sine oculis act downstream of or in parallel with Hedgehog signaling and (3) the Hedgehog signaling pathway required for Bolwig's organ development is a new type and lacks Fused kinase and Cubitus interruptus as downstream components.

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Interaction between EGFR signaling and DE-cadherin during nervous system morphogenesis

Development ◽

10.1242/dev.129.17.3983 ◽

2002 ◽

Vol 129 (17) ◽

pp. 3983-3994 ◽

Cited By ~ 2

Author(s):

Karin Dumstrei ◽

Fay Wang ◽

Diana Shy ◽

Ulrich Tepass ◽

Volker Hartenstein

Keyword(s):

Cell Adhesion ◽

Visual System ◽

Egf Receptor ◽

Genetic Interaction ◽

Apoptotic Cell ◽

Egfr Signaling ◽

Surface Ectoderm ◽

Egfr Ligand ◽

Wingless Signaling ◽

Bolwig's Organ

Dynamically regulated cell adhesion plays an important role during animal morphogenesis. Here we use the formation of the visual system in Drosophila embryos as a model system to investigate the function of the Drosophila classic cadherin, DE-cadherin, which is encoded by the shotgun (shg) gene. The visual system is derived from the optic placode which normally invaginates from the surface ectoderm of the embryo and gives rise to two separate structures, the larval eye (Bolwig’s organ) and the optic lobe. The optic placode dissociates and undergoes apoptotic cell death in the absence of DE-cadherin, whereas overexpression of DE-cadherin results in the failure of optic placode cells to invaginate and of Bolwig’s organ precursors to separate from the placode. These findings indicate that dynamically regulated levels of DE-cadherin are essential for normal optic placode development. It was shown previously that overexpression of DE-cadherin can disrupt Wingless signaling through titration of Armadillo out of the cytoplasm to the membrane. However, the observed defects are likely the consequence of altered DE-cadherin mediated adhesion rather than a result of compromising Wingless signaling, as overexpression of a DE-cadherin-α-catenin fusion protein, which lacks Armadillo binding sites, causes similar defects as DE-cadherin overexpression. We further studied the genetic interaction between DE-cadherin and the Drosophila EGF receptor homolog, EGFR. If EGFR function is eliminated, optic placode defects resemble those following DE-cadherin overexpression, which suggests that loss of EGFR results in an increased adhesion of optic placode cells. An interaction between EGFR and DE-cadherin is further supported by the finding that expression of a constitutively active EGFR enhances the phenotype of a weak shg mutation, whereas a mutation in rhomboid (rho) (an activator of the EGFR ligand Spitz) partially suppresses the shg mutant phenotype. Finally, EGFR can be co-immunoprecipitated with anti-DE-cadherin and anti-Armadillo antibodies from embryonic protein extracts. We propose that EGFR signaling plays a role in morphogenesis by modulating cell adhesion.

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Neuroendocrine Control of Drosophila Larval Light Preference

Science ◽

10.1126/science.1241210 ◽

2013 ◽

Vol 341 (6150) ◽

pp. 1113-1116 ◽

Cited By ~ 60

Author(s):

Naoki Yamanaka ◽

Nuria M. Romero ◽

Francisco A. Martin ◽

Kim F. Rewitz ◽

Mu Sun ◽

...

Keyword(s):

Drosophila Melanogaster ◽

Adult Development ◽

Juvenile Stage ◽

Neuroendocrine Control ◽

Animal Development ◽

Bolwig's Organ ◽

Innate Behaviors ◽

Light Avoidance ◽

Light Preference ◽

Class Iv

Animal development is coupled with innate behaviors that maximize chances of survival. Here, we show that the prothoracicotropic hormone (PTTH), a neuropeptide that controls the developmental transition from juvenile stage to sexual maturation, also regulates light avoidance in Drosophila melanogaster larvae. PTTH, through its receptor Torso, acts on two light sensors—the Bolwig’s organ and the peripheral class IV dendritic arborization neurons—to regulate light avoidance. We found that PTTH concomitantly promotes steroidogenesis and light avoidance at the end of larval stage, driving animals toward a darker environment to initiate the immobile maturation phase. Thus, PTTH controls the decisions of when and where animals undergo metamorphosis, optimizing conditions for adult development.

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sine oculis is a homeobox gene required for Drosophila visual system development.

Genetics ◽

10.1093/genetics/138.4.1137 ◽

1994 ◽

Vol 138 (4) ◽

pp. 1137-1150 ◽

Cited By ~ 3

Author(s):

M A Serikaku ◽

J E O'Tousa

Keyword(s):

Embryonic Development ◽

Visual System ◽

Gene Product ◽

Optic Lobe ◽

System Development ◽

Photoreceptor Cells ◽

P Element ◽

Sine Oculis ◽

Visual System Development ◽

Bolwig's Organ

Abstract The somda (sine oculis-medusa) mutant is the result of a P element insertion at position 43C on the second chromosome. somda causes aberrant development of the larval photoreceptor (Bolwig's) organ and the optic lobe primordium in the embryo. Later in development, adult photoreceptors fail to project axons into the optic ganglion. Consequently optic lobe development is aborted and photoreceptor cells show age-dependent retinal degeneration. The so gene was isolated and characterized. The gene encodes a homeodomain protein expressed in the optic lobe primordium and Bolwig's organ of embryos, in the developing adult visual system of larvae, and in photoreceptor cells and optic lobes of adults. In addition, the SO product is found at invagination sites during embryonic development: at the stomadeal invagination, the cephalic furrow, and at segmental boundaries. The mutant somda allele causes severe reduction of SO embryonic expression but maintains adult visual system expression. Ubiquitous expression of the SO gene product in 4-8-hr embryos rescues all somda mutant abnormalities, including the adult phenotypes. Thus, all deficits in adult visual system development and function results from failure to properly express the so gene during embryonic development. This analysis shows that the homeodomain containing SO gene product is involved in the specification of the larval and adult visual system development during embryogenesis.

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Embryonic Expression of the Divergent Drosophila β3-Tubulin Isoform Is Required for Larval Behavior

Genetics ◽

10.1093/genetics/158.1.253 ◽

2001 ◽

Vol 158 (1) ◽

pp. 253-263 ◽

Cited By ~ 1

Author(s):

Robert W Dettman ◽

F Rudolf Turner ◽

Henry D Hoyle ◽

Elizabeth C Raff

Keyword(s):

Differential Expression ◽

Larval Stage ◽

Larval Behavior ◽

Microtubule Organization ◽

Microtubule Cytoskeleton ◽

Behavioral Abnormalities ◽

Gut Function ◽

Different Types ◽

Bolwig's Organ ◽

Larval Lethality

Abstract We have sought to define the developmental and cellular roles played by differential expression of distinct β-tubulins. Drosophila β3-tubulin (β3) is a structurally divergent isoform transiently expressed during midembryogenesis. Severe β3 mutations cause larval lethality resulting from failed gut function and consequent starvation. However, mutant larvae also display behavioral abnormalities consistent with defective sensory perception. We identified embryonic β3 expression in several previously undefined sites, including different types of sensory organs. We conclude that abnormalities in foraging behavior and photoresponsiveness exhibited by prelethal mutant larvae reflect defective β3 function in the embryo during development of chordotonal and other mechanosensory organs and of Bolwig’s organ and nerve. We show that microtubule organization in the cap cells of chordotonal organs is altered in mutant larvae. Thus transient zygotic β3 expression has permanent consequences for the architecture of the cap cell microtubule cytoskeleton in the larval sensilla, even when β3 is no longer present. Our data provide a link between the microtubule cytoskeleton in embryogenesis and the behavioral phenotype manifested as defective proprioreception at the larval stage.

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The control of cell fate in the embryonic visual system by atonal, tailless and EGFR signaling

Development ◽

10.1242/dev.126.13.2945 ◽

1999 ◽

Vol 126 (13) ◽

pp. 2945-2954 ◽

Cited By ~ 5

Author(s):

A. Daniel ◽

K. Dumstrei ◽

J.A. Lengyel ◽

V. Hartenstein

Keyword(s):

Visual System ◽

Cell Fate ◽

Optic Lobe ◽

Egfr Signaling ◽

Phenotypic Analysis ◽

Eyes Absent ◽

Sine Oculis ◽

Bolwig's Organ ◽

Encoding Genes

We describe here the role of the transcription factors encoding genes tailless (tll), atonal (ato), sine oculis (so), eyeless (ey) and eyes absent (eya), and EGFR signaling in establishing the Drosophila embryonic visual system. The embryonic visual system consists of the optic lobe primordium, which, during later larval life, develops into the prominent optic lobe neuropiles, and the larval photoreceptor (Bolwig's organ). Both structures derive from a neurectodermal placode in the embryonic head. Expression of tll is normally confined to the optic lobe primordium, whereas ato appears in a subset of Bolwig's organ cells that we call Bolwig's organ founders. Phenotypic analysis, using specific markers for Bolwig's organ and the optic lobe, of tll loss- and gain-of-function mutant embryos reveals that tll functions to drive cells to optic lobe as opposed to Bolwig's organ fate. Similar experiments indicate that ato has the opposite effect, namely driving cells to a Bolwig's organ fate. Since we can show that tll and ato do not regulate each other, we propose a model wherein tll expression restricts the ability of cells to respond to signaling arising from ato-expressing Bolwig's organ pioneers. Our data further suggest that the Bolwig's organ founder cells produce Spitz (the Drosophila TGFalpha homolog) signal, which is passed to the neighboring secondary Bolwig's organ cells where it activates the EGFR signaling cascade and maintains the fate of these secondary cells. The regulators of tll expression in the embryonic visual system remain elusive, as we were unable to find evidence for regulation by the ‘early eye genes’ so, eya and ey, or by EGFR signaling.

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