Cargando…

Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling

The pattern of the Drosophila melanogaster adult wing is heavily influenced by the expression of proteins that dictate cell fate decisions between intervein and vein during development. dSRF (Blistered) expression in specific regions of the larval wing disc promotes intervein cell fate, whereas EGFR...

Descripción completa

Detalles Bibliográficos
Autores principales: Klebanow, Lindsey R., Peshel, Emanuela C., Schuster, Andrew T., De, Kuntal, Sarvepalli, Kavitha, Lemieux, Madeleine E., Lenoir, Jessica J., Moore, Adrian W., McDonald, Jocelyn A., Longworth, Michelle S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004906/
https://www.ncbi.nlm.nih.gov/pubmed/27317808
http://dx.doi.org/10.1242/dev.133686
_version_ 1782450839258923008
author Klebanow, Lindsey R.
Peshel, Emanuela C.
Schuster, Andrew T.
De, Kuntal
Sarvepalli, Kavitha
Lemieux, Madeleine E.
Lenoir, Jessica J.
Moore, Adrian W.
McDonald, Jocelyn A.
Longworth, Michelle S.
author_facet Klebanow, Lindsey R.
Peshel, Emanuela C.
Schuster, Andrew T.
De, Kuntal
Sarvepalli, Kavitha
Lemieux, Madeleine E.
Lenoir, Jessica J.
Moore, Adrian W.
McDonald, Jocelyn A.
Longworth, Michelle S.
author_sort Klebanow, Lindsey R.
collection PubMed
description The pattern of the Drosophila melanogaster adult wing is heavily influenced by the expression of proteins that dictate cell fate decisions between intervein and vein during development. dSRF (Blistered) expression in specific regions of the larval wing disc promotes intervein cell fate, whereas EGFR activity promotes vein cell fate. Here, we report that the chromatin-organizing protein CAP-D3 acts to dampen dSRF levels at the anterior/posterior boundary in the larval wing disc, promoting differentiation of cells into the anterior crossvein. CAP-D3 represses KNOT expression in cells immediately adjacent to the anterior/posterior boundary, thus blocking KNOT-mediated repression of EGFR activity and preventing cell death. Maintenance of EGFR activity in these cells depresses dSRF levels in the neighboring anterior crossvein progenitor cells, allowing them to differentiate into vein cells. These findings uncover a novel transcriptional regulatory network influencing Drosophila wing vein development, and are the first to identify a Condensin II subunit as an important regulator of EGFR activity and cell fate determination in vivo.
format Online
Article
Text
id pubmed-5004906
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-50049062016-09-13 Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling Klebanow, Lindsey R. Peshel, Emanuela C. Schuster, Andrew T. De, Kuntal Sarvepalli, Kavitha Lemieux, Madeleine E. Lenoir, Jessica J. Moore, Adrian W. McDonald, Jocelyn A. Longworth, Michelle S. Development Research Article The pattern of the Drosophila melanogaster adult wing is heavily influenced by the expression of proteins that dictate cell fate decisions between intervein and vein during development. dSRF (Blistered) expression in specific regions of the larval wing disc promotes intervein cell fate, whereas EGFR activity promotes vein cell fate. Here, we report that the chromatin-organizing protein CAP-D3 acts to dampen dSRF levels at the anterior/posterior boundary in the larval wing disc, promoting differentiation of cells into the anterior crossvein. CAP-D3 represses KNOT expression in cells immediately adjacent to the anterior/posterior boundary, thus blocking KNOT-mediated repression of EGFR activity and preventing cell death. Maintenance of EGFR activity in these cells depresses dSRF levels in the neighboring anterior crossvein progenitor cells, allowing them to differentiate into vein cells. These findings uncover a novel transcriptional regulatory network influencing Drosophila wing vein development, and are the first to identify a Condensin II subunit as an important regulator of EGFR activity and cell fate determination in vivo. The Company of Biologists Ltd 2016-08-01 /pmc/articles/PMC5004906/ /pubmed/27317808 http://dx.doi.org/10.1242/dev.133686 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Klebanow, Lindsey R.
Peshel, Emanuela C.
Schuster, Andrew T.
De, Kuntal
Sarvepalli, Kavitha
Lemieux, Madeleine E.
Lenoir, Jessica J.
Moore, Adrian W.
McDonald, Jocelyn A.
Longworth, Michelle S.
Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title_full Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title_fullStr Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title_full_unstemmed Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title_short Drosophila Condensin II subunit Chromosome-associated protein D3 regulates cell fate determination through non-cell-autonomous signaling
title_sort drosophila condensin ii subunit chromosome-associated protein d3 regulates cell fate determination through non-cell-autonomous signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004906/
https://www.ncbi.nlm.nih.gov/pubmed/27317808
http://dx.doi.org/10.1242/dev.133686
work_keys_str_mv AT klebanowlindseyr drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT peshelemanuelac drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT schusterandrewt drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT dekuntal drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT sarvepallikavitha drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT lemieuxmadeleinee drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT lenoirjessicaj drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT mooreadrianw drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT mcdonaldjocelyna drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling
AT longworthmichelles drosophilacondensiniisubunitchromosomeassociatedproteind3regulatescellfatedeterminationthroughnoncellautonomoussignaling