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Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs
Embryonic development depends on a highly coordinated shift in transcription programs known as the maternal-to-zygotic transition (MZT). It remains unclear how haploid and diploid embryo coordinate their genomic activation and embryonic development during MZT in haplodiploid animals. Here, we applie...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377728/ https://www.ncbi.nlm.nih.gov/pubmed/34422813 http://dx.doi.org/10.3389/fcell.2021.690167 |
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author | Wang, Miao Chen, Dong Zheng, Huoqing Zhao, Liuwei Xue, Xiaofeng Yu, Fengyun Zhang, Yu Cheng, Chao Niu, Qingsheng Wang, Shuai Zhang, Yi Wu, Liming |
author_facet | Wang, Miao Chen, Dong Zheng, Huoqing Zhao, Liuwei Xue, Xiaofeng Yu, Fengyun Zhang, Yu Cheng, Chao Niu, Qingsheng Wang, Shuai Zhang, Yi Wu, Liming |
author_sort | Wang, Miao |
collection | PubMed |
description | Embryonic development depends on a highly coordinated shift in transcription programs known as the maternal-to-zygotic transition (MZT). It remains unclear how haploid and diploid embryo coordinate their genomic activation and embryonic development during MZT in haplodiploid animals. Here, we applied a single-embryo RNA-seq approach to characterize the embryonic transcriptome dynamics in haploid males vs. diploid females of the haplodiploid insect honeybee (Apis mellifera). We observed typical zygotic genome activation (ZGA) occurred in three major waves specifically in female honeybee embryos; haploid genome activation was much weaker and occurred later. Strikingly, we also observed three waves of transcriptional activation for thousands of long non-coding transcripts (lncRNA), 73% of which are transcribed from intronic regions and 65% were specific to female honeybee embryos. These findings support a model in which introns encode thousands of lncRNAs that are expressed in a diploid-embryo-specific and ZGA-triggered manner that may have potential functions to regulate gene expression during early embryonic development in the haplodiploid insect honeybee. |
format | Online Article Text |
id | pubmed-8377728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83777282021-08-21 Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs Wang, Miao Chen, Dong Zheng, Huoqing Zhao, Liuwei Xue, Xiaofeng Yu, Fengyun Zhang, Yu Cheng, Chao Niu, Qingsheng Wang, Shuai Zhang, Yi Wu, Liming Front Cell Dev Biol Cell and Developmental Biology Embryonic development depends on a highly coordinated shift in transcription programs known as the maternal-to-zygotic transition (MZT). It remains unclear how haploid and diploid embryo coordinate their genomic activation and embryonic development during MZT in haplodiploid animals. Here, we applied a single-embryo RNA-seq approach to characterize the embryonic transcriptome dynamics in haploid males vs. diploid females of the haplodiploid insect honeybee (Apis mellifera). We observed typical zygotic genome activation (ZGA) occurred in three major waves specifically in female honeybee embryos; haploid genome activation was much weaker and occurred later. Strikingly, we also observed three waves of transcriptional activation for thousands of long non-coding transcripts (lncRNA), 73% of which are transcribed from intronic regions and 65% were specific to female honeybee embryos. These findings support a model in which introns encode thousands of lncRNAs that are expressed in a diploid-embryo-specific and ZGA-triggered manner that may have potential functions to regulate gene expression during early embryonic development in the haplodiploid insect honeybee. Frontiers Media S.A. 2021-08-06 /pmc/articles/PMC8377728/ /pubmed/34422813 http://dx.doi.org/10.3389/fcell.2021.690167 Text en Copyright © 2021 Wang, Chen, Zheng, Zhao, Xue, Yu, Zhang, Cheng, Niu, Wang, Zhang and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Wang, Miao Chen, Dong Zheng, Huoqing Zhao, Liuwei Xue, Xiaofeng Yu, Fengyun Zhang, Yu Cheng, Chao Niu, Qingsheng Wang, Shuai Zhang, Yi Wu, Liming Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title | Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title_full | Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title_fullStr | Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title_full_unstemmed | Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title_short | Sex-Specific Development in Haplodiploid Honeybee Is Controlled by the Female-Embryo-Specific Activation of Thousands of Intronic LncRNAs |
title_sort | sex-specific development in haplodiploid honeybee is controlled by the female-embryo-specific activation of thousands of intronic lncrnas |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377728/ https://www.ncbi.nlm.nih.gov/pubmed/34422813 http://dx.doi.org/10.3389/fcell.2021.690167 |
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