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Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan

Asymmetric cell division is a ubiquitous feature during the development of higher organisms. Asymmetry is achieved by differential localization or activities of biological molecules such as proteins, and coding and non-coding RNAs. Here, we present subcellular transcriptomic and proteomic analyses a...

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Autores principales: Sindelka, Radek, Abaffy, Pavel, Qu, Yanyan, Tomankova, Silvie, Sidova, Monika, Naraine, Ravindra, Kolar, Michal, Peuchen, Elizabeth, Sun, Liangliang, Dovichi, Norman, Kubista, Mikael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974320/
https://www.ncbi.nlm.nih.gov/pubmed/29844480
http://dx.doi.org/10.1038/s41598-018-26592-1
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author Sindelka, Radek
Abaffy, Pavel
Qu, Yanyan
Tomankova, Silvie
Sidova, Monika
Naraine, Ravindra
Kolar, Michal
Peuchen, Elizabeth
Sun, Liangliang
Dovichi, Norman
Kubista, Mikael
author_facet Sindelka, Radek
Abaffy, Pavel
Qu, Yanyan
Tomankova, Silvie
Sidova, Monika
Naraine, Ravindra
Kolar, Michal
Peuchen, Elizabeth
Sun, Liangliang
Dovichi, Norman
Kubista, Mikael
author_sort Sindelka, Radek
collection PubMed
description Asymmetric cell division is a ubiquitous feature during the development of higher organisms. Asymmetry is achieved by differential localization or activities of biological molecules such as proteins, and coding and non-coding RNAs. Here, we present subcellular transcriptomic and proteomic analyses along the animal-vegetal axis of Xenopus laevis eggs. More than 98% of the maternal mRNAs could be categorized into four localization profile groups: animal, vegetal, extremely vegetal, and a newly described group of mRNAs that we call extremely animal, which are mRNAs enriched in the animal cortex region. 3′UTRs of localized mRNAs were analyzed for localization motifs. Several putative motifs were discovered for vegetal and extremely vegetal mRNAs, while no distinct conserved motifs for the extremely animal mRNAs were identified, suggesting different localization mechanisms. Asymmetric profiles were also found for proteins, with correlation to those of corresponding mRNAs. Based on unexpected observation of the profiles of the homoeologous genes exd2 we propose a possible mechanism of genetic evolution.
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spelling pubmed-59743202018-05-31 Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan Sindelka, Radek Abaffy, Pavel Qu, Yanyan Tomankova, Silvie Sidova, Monika Naraine, Ravindra Kolar, Michal Peuchen, Elizabeth Sun, Liangliang Dovichi, Norman Kubista, Mikael Sci Rep Article Asymmetric cell division is a ubiquitous feature during the development of higher organisms. Asymmetry is achieved by differential localization or activities of biological molecules such as proteins, and coding and non-coding RNAs. Here, we present subcellular transcriptomic and proteomic analyses along the animal-vegetal axis of Xenopus laevis eggs. More than 98% of the maternal mRNAs could be categorized into four localization profile groups: animal, vegetal, extremely vegetal, and a newly described group of mRNAs that we call extremely animal, which are mRNAs enriched in the animal cortex region. 3′UTRs of localized mRNAs were analyzed for localization motifs. Several putative motifs were discovered for vegetal and extremely vegetal mRNAs, while no distinct conserved motifs for the extremely animal mRNAs were identified, suggesting different localization mechanisms. Asymmetric profiles were also found for proteins, with correlation to those of corresponding mRNAs. Based on unexpected observation of the profiles of the homoeologous genes exd2 we propose a possible mechanism of genetic evolution. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974320/ /pubmed/29844480 http://dx.doi.org/10.1038/s41598-018-26592-1 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
Sindelka, Radek
Abaffy, Pavel
Qu, Yanyan
Tomankova, Silvie
Sidova, Monika
Naraine, Ravindra
Kolar, Michal
Peuchen, Elizabeth
Sun, Liangliang
Dovichi, Norman
Kubista, Mikael
Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title_full Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title_fullStr Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title_full_unstemmed Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title_short Asymmetric distribution of biomolecules of maternal origin in the Xenopus laevis egg and their impact on the developmental plan
title_sort asymmetric distribution of biomolecules of maternal origin in the xenopus laevis egg and their impact on the developmental plan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974320/
https://www.ncbi.nlm.nih.gov/pubmed/29844480
http://dx.doi.org/10.1038/s41598-018-26592-1
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