dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.

Proper organ patterning depends on a tight coordination between cell proliferation and differentiation. The patterning of Drosophila retina occurs both very fast and with high precision. This process is driven by the dynamic changes in signaling activity of the conserved Hedgehog (Hh) pathway, which...

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Main Authors: Catarina Brás-Pereira, Delphine Potier, Jelle Jacobs, Stein Aerts, Fernando Casares, Florence Janody
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4956209?pdf=render
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spelling doaj-5635e6f747d2444d9b2fe8d2e38f8b402020-11-25T02:06:06ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042016-07-01127e100620410.1371/journal.pgen.1006204dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.Catarina Brás-PereiraDelphine PotierJelle JacobsStein AertsFernando CasaresFlorence JanodyProper organ patterning depends on a tight coordination between cell proliferation and differentiation. The patterning of Drosophila retina occurs both very fast and with high precision. This process is driven by the dynamic changes in signaling activity of the conserved Hedgehog (Hh) pathway, which coordinates cell fate determination, cell cycle and tissue morphogenesis. Here we show that during Drosophila retinogenesis, the retinal determination gene dachshund (dac) is not only a target of the Hh signaling pathway, but is also a modulator of its activity. Using developmental genetics techniques, we demonstrate that dac enhances Hh signaling by promoting the accumulation of the Gli transcription factor Cubitus interruptus (Ci) parallel to or downstream of fused. In the absence of dac, all Hh-mediated events associated to the morphogenetic furrow are delayed. One of the consequences is that, posterior to the furrow, dac- cells cannot activate a Roadkill-Cullin3 negative feedback loop that attenuates Hh signaling and which is necessary for retinal cells to continue normal differentiation. Therefore, dac is part of an essential positive feedback loop in the Hh pathway, guaranteeing the speed and the accuracy of Drosophila retinogenesis.http://europepmc.org/articles/PMC4956209?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Catarina Brás-Pereira
Delphine Potier
Jelle Jacobs
Stein Aerts
Fernando Casares
Florence Janody
spellingShingle Catarina Brás-Pereira
Delphine Potier
Jelle Jacobs
Stein Aerts
Fernando Casares
Florence Janody
dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
PLoS Genetics
author_facet Catarina Brás-Pereira
Delphine Potier
Jelle Jacobs
Stein Aerts
Fernando Casares
Florence Janody
author_sort Catarina Brás-Pereira
title dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
title_short dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
title_full dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
title_fullStr dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
title_full_unstemmed dachshund Potentiates Hedgehog Signaling during Drosophila Retinogenesis.
title_sort dachshund potentiates hedgehog signaling during drosophila retinogenesis.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2016-07-01
description Proper organ patterning depends on a tight coordination between cell proliferation and differentiation. The patterning of Drosophila retina occurs both very fast and with high precision. This process is driven by the dynamic changes in signaling activity of the conserved Hedgehog (Hh) pathway, which coordinates cell fate determination, cell cycle and tissue morphogenesis. Here we show that during Drosophila retinogenesis, the retinal determination gene dachshund (dac) is not only a target of the Hh signaling pathway, but is also a modulator of its activity. Using developmental genetics techniques, we demonstrate that dac enhances Hh signaling by promoting the accumulation of the Gli transcription factor Cubitus interruptus (Ci) parallel to or downstream of fused. In the absence of dac, all Hh-mediated events associated to the morphogenetic furrow are delayed. One of the consequences is that, posterior to the furrow, dac- cells cannot activate a Roadkill-Cullin3 negative feedback loop that attenuates Hh signaling and which is necessary for retinal cells to continue normal differentiation. Therefore, dac is part of an essential positive feedback loop in the Hh pathway, guaranteeing the speed and the accuracy of Drosophila retinogenesis.
url http://europepmc.org/articles/PMC4956209?pdf=render
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