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Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development
Organisms that have evolved alternative modes of reproduction, complementary to the sexual mode, are found across metazoans. The chordate Botryllus schlosseri is an emerging model for asexual development studies. Botryllus can rebuild its entire body from a portion of adult epithelia in a continuous...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893630/ https://www.ncbi.nlm.nih.gov/pubmed/27264734 http://dx.doi.org/10.1038/srep27357 |
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author | Ricci, Lorenzo Chaurasia, Ankita Lapébie, Pascal Dru, Philippe Helm, Rebecca R. Copley, Richard R. Tiozzo, Stefano |
author_facet | Ricci, Lorenzo Chaurasia, Ankita Lapébie, Pascal Dru, Philippe Helm, Rebecca R. Copley, Richard R. Tiozzo, Stefano |
author_sort | Ricci, Lorenzo |
collection | PubMed |
description | Organisms that have evolved alternative modes of reproduction, complementary to the sexual mode, are found across metazoans. The chordate Botryllus schlosseri is an emerging model for asexual development studies. Botryllus can rebuild its entire body from a portion of adult epithelia in a continuous and stereotyped process called blastogenesis. Anatomy and ontogenies of blastogenesis are well described, however molecular signatures triggering this developmental process are entirely unknown. We isolated tissues at the site of blastogenesis onset and from the same epithelia where this process is never triggered. We linearly amplified an ultra-low amount of mRNA (<10ng) and generated three transcriptome datasets. To provide a conservative landscape of transcripts differentially expressed between blastogenic vs. non-blastogenic epithelia we compared three different mapping and analysis strategies with a de novo assembled transcriptome and partially assembled genome as references, additionally a self-mapping strategy on the dataset. A subset of differentially expressed genes were analyzed and validated by in situ hybridization. The comparison of different analyses allowed us to isolate stringent sets of target genes, including transcripts with potential involvement in the onset of a non-embryonic developmental pathway. The results provide a good entry point to approach regenerative event in a basal chordate. |
format | Online Article Text |
id | pubmed-4893630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48936302016-06-10 Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development Ricci, Lorenzo Chaurasia, Ankita Lapébie, Pascal Dru, Philippe Helm, Rebecca R. Copley, Richard R. Tiozzo, Stefano Sci Rep Article Organisms that have evolved alternative modes of reproduction, complementary to the sexual mode, are found across metazoans. The chordate Botryllus schlosseri is an emerging model for asexual development studies. Botryllus can rebuild its entire body from a portion of adult epithelia in a continuous and stereotyped process called blastogenesis. Anatomy and ontogenies of blastogenesis are well described, however molecular signatures triggering this developmental process are entirely unknown. We isolated tissues at the site of blastogenesis onset and from the same epithelia where this process is never triggered. We linearly amplified an ultra-low amount of mRNA (<10ng) and generated three transcriptome datasets. To provide a conservative landscape of transcripts differentially expressed between blastogenic vs. non-blastogenic epithelia we compared three different mapping and analysis strategies with a de novo assembled transcriptome and partially assembled genome as references, additionally a self-mapping strategy on the dataset. A subset of differentially expressed genes were analyzed and validated by in situ hybridization. The comparison of different analyses allowed us to isolate stringent sets of target genes, including transcripts with potential involvement in the onset of a non-embryonic developmental pathway. The results provide a good entry point to approach regenerative event in a basal chordate. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4893630/ /pubmed/27264734 http://dx.doi.org/10.1038/srep27357 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ricci, Lorenzo Chaurasia, Ankita Lapébie, Pascal Dru, Philippe Helm, Rebecca R. Copley, Richard R. Tiozzo, Stefano Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title | Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title_full | Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title_fullStr | Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title_full_unstemmed | Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title_short | Identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
title_sort | identification of differentially expressed genes from multipotent epithelia at the onset of an asexual development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893630/ https://www.ncbi.nlm.nih.gov/pubmed/27264734 http://dx.doi.org/10.1038/srep27357 |
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