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Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals

Hox genes are highly conserved transcription factors renowned for their roles in the segmental patterning of the embryonic anterior-posterior (A/P) axis. We report functions for Hox genes in A/P tissue segmentation and transverse fission behavior underlying asexual reproduction in adult planarian fl...

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Autores principales: Arnold, Christopher P., Lozano, Analí Migueles, Mann, Frederick G., Nowotarski, Stephanie H., Haug, Julianna O., Lange, Jeffrey J., Seidel, Chris W., Alvarado, Alejandro Sánchez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602322/
https://www.ncbi.nlm.nih.gov/pubmed/34795249
http://dx.doi.org/10.1038/s41467-021-26986-2
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author Arnold, Christopher P.
Lozano, Analí Migueles
Mann, Frederick G.
Nowotarski, Stephanie H.
Haug, Julianna O.
Lange, Jeffrey J.
Seidel, Chris W.
Alvarado, Alejandro Sánchez
author_facet Arnold, Christopher P.
Lozano, Analí Migueles
Mann, Frederick G.
Nowotarski, Stephanie H.
Haug, Julianna O.
Lange, Jeffrey J.
Seidel, Chris W.
Alvarado, Alejandro Sánchez
author_sort Arnold, Christopher P.
collection PubMed
description Hox genes are highly conserved transcription factors renowned for their roles in the segmental patterning of the embryonic anterior-posterior (A/P) axis. We report functions for Hox genes in A/P tissue segmentation and transverse fission behavior underlying asexual reproduction in adult planarian flatworms, Schmidtea mediterranea. Silencing of each of the Hox family members identifies 5 Hox genes required for asexual reproduction. Among these, silencing of hox3 genes results in supernumerary fission segments, while silencing of post2b eliminates segmentation altogether. The opposing roles of hox3 and post2b in segmentation are paralleled in their respective regulation of fission behavior. Silencing of hox3 increases the frequency of fission behavior initiation while silencing of post2b eliminates fission behavior entirely. Furthermore, we identify a network of downstream effector genes mediating Hox gene functions, providing insight into their respective mechanisms of action. In particular, we resolve roles for post2b and effector genes in the functions of the marginal adhesive organ in fission behavior regulation. Collectively, our study establishes adult stage roles for Hox genes in the regulation of tissue segmentation and behavior associated with asexual reproduction.
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spelling pubmed-86023222021-11-19 Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals Arnold, Christopher P. Lozano, Analí Migueles Mann, Frederick G. Nowotarski, Stephanie H. Haug, Julianna O. Lange, Jeffrey J. Seidel, Chris W. Alvarado, Alejandro Sánchez Nat Commun Article Hox genes are highly conserved transcription factors renowned for their roles in the segmental patterning of the embryonic anterior-posterior (A/P) axis. We report functions for Hox genes in A/P tissue segmentation and transverse fission behavior underlying asexual reproduction in adult planarian flatworms, Schmidtea mediterranea. Silencing of each of the Hox family members identifies 5 Hox genes required for asexual reproduction. Among these, silencing of hox3 genes results in supernumerary fission segments, while silencing of post2b eliminates segmentation altogether. The opposing roles of hox3 and post2b in segmentation are paralleled in their respective regulation of fission behavior. Silencing of hox3 increases the frequency of fission behavior initiation while silencing of post2b eliminates fission behavior entirely. Furthermore, we identify a network of downstream effector genes mediating Hox gene functions, providing insight into their respective mechanisms of action. In particular, we resolve roles for post2b and effector genes in the functions of the marginal adhesive organ in fission behavior regulation. Collectively, our study establishes adult stage roles for Hox genes in the regulation of tissue segmentation and behavior associated with asexual reproduction. Nature Publishing Group UK 2021-11-18 /pmc/articles/PMC8602322/ /pubmed/34795249 http://dx.doi.org/10.1038/s41467-021-26986-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Arnold, Christopher P.
Lozano, Analí Migueles
Mann, Frederick G.
Nowotarski, Stephanie H.
Haug, Julianna O.
Lange, Jeffrey J.
Seidel, Chris W.
Alvarado, Alejandro Sánchez
Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title_full Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title_fullStr Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title_full_unstemmed Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title_short Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
title_sort hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602322/
https://www.ncbi.nlm.nih.gov/pubmed/34795249
http://dx.doi.org/10.1038/s41467-021-26986-2
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