Cargando…

Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation

Germ cells in Drosophila melanogaster are specified maternally shortly after fertilization and are transcriptionally quiescent until their zygotic genome is activated to sustain further development. To understand the molecular basis of this process, we analyzed the progressing transcriptomes of earl...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yi-Ru, Lai, Hsiao Wen, Huang, Hsiao Han, Chen, Hsing-Chun, Fugmann, Sebastian D., Yang, Shu Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168578/
https://www.ncbi.nlm.nih.gov/pubmed/33858841
http://dx.doi.org/10.1101/gr.271148.120
_version_ 1783701902918156288
author Li, Yi-Ru
Lai, Hsiao Wen
Huang, Hsiao Han
Chen, Hsing-Chun
Fugmann, Sebastian D.
Yang, Shu Yuan
author_facet Li, Yi-Ru
Lai, Hsiao Wen
Huang, Hsiao Han
Chen, Hsing-Chun
Fugmann, Sebastian D.
Yang, Shu Yuan
author_sort Li, Yi-Ru
collection PubMed
description Germ cells in Drosophila melanogaster are specified maternally shortly after fertilization and are transcriptionally quiescent until their zygotic genome is activated to sustain further development. To understand the molecular basis of this process, we analyzed the progressing transcriptomes of early male and female germ cells at the single-cell level between germline specification and coalescence with somatic gonadal cells. Our data comprehensively cover zygotic activation in the germline genome, and analyses on genes that exhibit germline-restricted expression reveal that polymerase pausing and differential RNA stability are important mechanisms that establish gene expression differences between the germline and soma. In addition, we observe an immediate bifurcation between the male and female germ cells as zygotic transcription begins. The main difference between the two sexes is an elevation in X Chromosome expression in females relative to males, signifying incomplete dosage compensation, with a few select genes exhibiting even higher expression increases. These indicate that the male program is the default mode in the germline that is driven to female development with a second X Chromosome.
format Online
Article
Text
id pubmed-8168578
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-81685782021-12-01 Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation Li, Yi-Ru Lai, Hsiao Wen Huang, Hsiao Han Chen, Hsing-Chun Fugmann, Sebastian D. Yang, Shu Yuan Genome Res Research Germ cells in Drosophila melanogaster are specified maternally shortly after fertilization and are transcriptionally quiescent until their zygotic genome is activated to sustain further development. To understand the molecular basis of this process, we analyzed the progressing transcriptomes of early male and female germ cells at the single-cell level between germline specification and coalescence with somatic gonadal cells. Our data comprehensively cover zygotic activation in the germline genome, and analyses on genes that exhibit germline-restricted expression reveal that polymerase pausing and differential RNA stability are important mechanisms that establish gene expression differences between the germline and soma. In addition, we observe an immediate bifurcation between the male and female germ cells as zygotic transcription begins. The main difference between the two sexes is an elevation in X Chromosome expression in females relative to males, signifying incomplete dosage compensation, with a few select genes exhibiting even higher expression increases. These indicate that the male program is the default mode in the germline that is driven to female development with a second X Chromosome. Cold Spring Harbor Laboratory Press 2021-06 /pmc/articles/PMC8168578/ /pubmed/33858841 http://dx.doi.org/10.1101/gr.271148.120 Text en © 2021 Li et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Li, Yi-Ru
Lai, Hsiao Wen
Huang, Hsiao Han
Chen, Hsing-Chun
Fugmann, Sebastian D.
Yang, Shu Yuan
Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title_full Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title_fullStr Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title_full_unstemmed Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title_short Trajectory mapping of the early Drosophila germline reveals controls of zygotic activation and sex differentiation
title_sort trajectory mapping of the early drosophila germline reveals controls of zygotic activation and sex differentiation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168578/
https://www.ncbi.nlm.nih.gov/pubmed/33858841
http://dx.doi.org/10.1101/gr.271148.120
work_keys_str_mv AT liyiru trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation
AT laihsiaowen trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation
AT huanghsiaohan trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation
AT chenhsingchun trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation
AT fugmannsebastiand trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation
AT yangshuyuan trajectorymappingoftheearlydrosophilagermlinerevealscontrolsofzygoticactivationandsexdifferentiation