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  Continuous transcriptome analysis reveals novel patterns of early gene expression in Drosophila embryos

Pérez-Mojica, J. E., Enders, L., Walsh, J., Lau, K. H., & Lempradl, A. (2023). Continuous transcriptome analysis reveals novel patterns of early gene expression in Drosophila embryos. Cell genomics, 3: 100265. doi: 10.1016/j.xgen.2023.100265.

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10.1016_j.xgen.2023.100265.pdf (Verlagsversion), 3MB
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 Urheber:
Pérez-Mojica, J Eduardo1, Autor
Enders, Lennart2, Autor
Walsh, Joseph1, Autor
Lau, Kin H1, Autor
Lempradl, Adelheid2, Autor           
Affiliations:
1External Organizations, ou_persistent22              
2Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243644              

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Schlagwörter: Drosophila; development; sex-specific transcription; single-embryo RNA sequencing; zygotic genome activation
 Zusammenfassung: The transformative events during early organismal development lay the foundation for body formation and long-term phenotype. The rapid progression of events and the limited material available present major barriers to studying these earliest stages of development. Herein, we report an operationally simple RNA sequencing approach for high-resolution, time-sensitive transcriptome analysis in early (≤3 h) Drosophila embryos. This method does not require embryo staging but relies on single-embryo RNA sequencing and transcriptome ordering along a developmental trajectory (pseudo-time). The resulting high-resolution, time-sensitive mRNA expression profiles reveal the exact onset of transcription and degradation for thousands of transcripts. Further, using sex-specific transcription signatures, embryos can be sexed directly, eliminating the need for Y chromosome genotyping and revealing patterns of sex-biased transcription from the beginning of zygotic transcription. Our data provide an unparalleled resolution of gene expression during early development and enhance the current understanding of early transcriptional processes.

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Sprache(n): eng - English
 Datum: 2023-02-152023-03-08
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1016/j.xgen.2023.100265
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Titel: Cell genomics
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Amsterdam : Elsevier
Seiten: - Band / Heft: 3 Artikelnummer: 100265 Start- / Endseite: - Identifikator: ISSN: 2666-979X
CoNE: https://pure.mpg.de/cone/journals/resource/2666-979X