Cargando…

Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc

The imaginal discs of the genetically tractable model organism Drosophila melanogaster have been used to study cell-fate specification and plasticity, including homeotic changes and regeneration-induced transdetermination. The identity of the reprogramming mechanisms that induce plasticity has been...

Descripción completa

Detalles Bibliográficos
Autores principales: Abidi, Syeda Nayab Fatima, Smith-Bolton, Rachel K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862905/
https://www.ncbi.nlm.nih.gov/pubmed/29563503
http://dx.doi.org/10.1038/s41598-018-23093-z
_version_ 1783308307510853632
author Abidi, Syeda Nayab Fatima
Smith-Bolton, Rachel K.
author_facet Abidi, Syeda Nayab Fatima
Smith-Bolton, Rachel K.
author_sort Abidi, Syeda Nayab Fatima
collection PubMed
description The imaginal discs of the genetically tractable model organism Drosophila melanogaster have been used to study cell-fate specification and plasticity, including homeotic changes and regeneration-induced transdetermination. The identity of the reprogramming mechanisms that induce plasticity has been of great interest in the field. Here we identify a change from antennal fate to eye fate induced by a Distal-less-GAL4 (DllGAL4) P-element insertion that is a mutant allele of Dll and expresses GAL4 in the antennal imaginal disc. While this fate change is not induced by tissue damage, it appears to be a hybrid of transdetermination and homeosis as the GAL4 expression causes upregulation of Wingless, and the Dll mutation is required for the fate change. Neither GAL4 expression nor a Dll mutation on its own is able to induce antenna-to-eye fate changes. This plasticity appears to be unique to the DllGAL4 line, possibly due to cellular stress induced by the high GAL4 expression combined with the severity of the Dll mutation. Thus, we propose that even in the absence of tissue damage, other forms of cellular stress caused by high GAL4 expression can induce determined cell fates to change, and selector gene mutations can sensitize the tissue to these transformations.
format Online
Article
Text
id pubmed-5862905
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58629052018-03-27 Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc Abidi, Syeda Nayab Fatima Smith-Bolton, Rachel K. Sci Rep Article The imaginal discs of the genetically tractable model organism Drosophila melanogaster have been used to study cell-fate specification and plasticity, including homeotic changes and regeneration-induced transdetermination. The identity of the reprogramming mechanisms that induce plasticity has been of great interest in the field. Here we identify a change from antennal fate to eye fate induced by a Distal-less-GAL4 (DllGAL4) P-element insertion that is a mutant allele of Dll and expresses GAL4 in the antennal imaginal disc. While this fate change is not induced by tissue damage, it appears to be a hybrid of transdetermination and homeosis as the GAL4 expression causes upregulation of Wingless, and the Dll mutation is required for the fate change. Neither GAL4 expression nor a Dll mutation on its own is able to induce antenna-to-eye fate changes. This plasticity appears to be unique to the DllGAL4 line, possibly due to cellular stress induced by the high GAL4 expression combined with the severity of the Dll mutation. Thus, we propose that even in the absence of tissue damage, other forms of cellular stress caused by high GAL4 expression can induce determined cell fates to change, and selector gene mutations can sensitize the tissue to these transformations. Nature Publishing Group UK 2018-03-21 /pmc/articles/PMC5862905/ /pubmed/29563503 http://dx.doi.org/10.1038/s41598-018-23093-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Abidi, Syeda Nayab Fatima
Smith-Bolton, Rachel K.
Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title_full Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title_fullStr Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title_full_unstemmed Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title_short Cell fate changes induced by a Distal-less enhancer-trap transgene in the Drosophila antennal imaginal disc
title_sort cell fate changes induced by a distal-less enhancer-trap transgene in the drosophila antennal imaginal disc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862905/
https://www.ncbi.nlm.nih.gov/pubmed/29563503
http://dx.doi.org/10.1038/s41598-018-23093-z
work_keys_str_mv AT abidisyedanayabfatima cellfatechangesinducedbyadistallessenhancertraptransgeneinthedrosophilaantennalimaginaldisc
AT smithboltonrachelk cellfatechangesinducedbyadistallessenhancertraptransgeneinthedrosophilaantennalimaginaldisc