A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.

Planarian regeneration requires positional information to specify the identity of tissues to be replaced as well as pluripotent neoblasts capable of differentiating into new cell types. We found that wounding elicits rapid expression of a gene encoding a Forkhead-family transcription factor, FoxD. W...

Full description

Bibliographic Details
Main Authors: M Lucila Scimone, Sylvain W Lapan, Peter W Reddien
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3886891?pdf=render
id doaj-0de535a53004446cb8cdce7534aa2879
record_format Article
spelling doaj-0de535a53004446cb8cdce7534aa28792020-11-25T00:24:21ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042014-01-01101e100399910.1371/journal.pgen.1003999A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.M Lucila ScimoneSylvain W LapanPeter W ReddienPlanarian regeneration requires positional information to specify the identity of tissues to be replaced as well as pluripotent neoblasts capable of differentiating into new cell types. We found that wounding elicits rapid expression of a gene encoding a Forkhead-family transcription factor, FoxD. Wound-induced FoxD expression is specific to the ventral midline, is regulated by Hedgehog signaling, and is neoblast-independent. FoxD is subsequently expressed within a medial subpopulation of neoblasts at wounds involving head regeneration. Ultimately, FoxD is co-expressed with multiple anterior markers at the anterior pole. Inhibition of FoxD with RNA interference (RNAi) results in the failure to specify neoblasts expressing anterior markers (notum and prep) and in anterior pole formation defects. FoxD(RNAi) animals fail to regenerate a new midline and to properly pattern the anterior blastema, consistent with a role for the anterior pole in organizing pattern of the regenerating head. Our results suggest that wound signaling activates a forkhead transcription factor at the midline and, if the head is absent, FoxD promotes specification of neoblasts at the prior midline for anterior pole regeneration.http://europepmc.org/articles/PMC3886891?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author M Lucila Scimone
Sylvain W Lapan
Peter W Reddien
spellingShingle M Lucila Scimone
Sylvain W Lapan
Peter W Reddien
A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
PLoS Genetics
author_facet M Lucila Scimone
Sylvain W Lapan
Peter W Reddien
author_sort M Lucila Scimone
title A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
title_short A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
title_full A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
title_fullStr A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
title_full_unstemmed A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
title_sort forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2014-01-01
description Planarian regeneration requires positional information to specify the identity of tissues to be replaced as well as pluripotent neoblasts capable of differentiating into new cell types. We found that wounding elicits rapid expression of a gene encoding a Forkhead-family transcription factor, FoxD. Wound-induced FoxD expression is specific to the ventral midline, is regulated by Hedgehog signaling, and is neoblast-independent. FoxD is subsequently expressed within a medial subpopulation of neoblasts at wounds involving head regeneration. Ultimately, FoxD is co-expressed with multiple anterior markers at the anterior pole. Inhibition of FoxD with RNA interference (RNAi) results in the failure to specify neoblasts expressing anterior markers (notum and prep) and in anterior pole formation defects. FoxD(RNAi) animals fail to regenerate a new midline and to properly pattern the anterior blastema, consistent with a role for the anterior pole in organizing pattern of the regenerating head. Our results suggest that wound signaling activates a forkhead transcription factor at the midline and, if the head is absent, FoxD promotes specification of neoblasts at the prior midline for anterior pole regeneration.
url http://europepmc.org/articles/PMC3886891?pdf=render
work_keys_str_mv AT mlucilascimone aforkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
AT sylvainwlapan aforkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
AT peterwreddien aforkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
AT mlucilascimone forkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
AT sylvainwlapan forkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
AT peterwreddien forkheadtranscriptionfactoriswoundinducedattheplanarianmidlineandrequiredforanteriorpoleregeneration
_version_ 1725352482858598400