2020
DOI: 10.1016/bs.ctdb.2019.11.004
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Setting up for gastrulation: D. melanogaster

Abstract: Drosophila melanogaster embryos develop initially as a syncytium of totipotent nuclei and subsequently, once cellularized, undergo morphogenetic movements associated with gastrulation to generate the three somatic germ layers of the embryo: mesoderm, ectoderm, and endoderm. In this chapter, we focus on the first phase of gastrulation in Drosophila involving patterning of early embryos when cells differentiate their gene expression programs. This patterning process requires coordination of multiple developmenta… Show more

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Cited by 17 publications
(20 citation statements)
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“…At this point, widespread zygotic gene expression is initiated. It is at this early stage of the developmental process of the Drosophila embryo that patterning along the AP and DV body axes is established (reviewed by Stathopoulos and Newcomb, 2020). Two maternally deposited morphogens, Bcd and Dl, are key factors that orchestrate this patterning process.…”
Section: Introductionmentioning
confidence: 99%
“…At this point, widespread zygotic gene expression is initiated. It is at this early stage of the developmental process of the Drosophila embryo that patterning along the AP and DV body axes is established (reviewed by Stathopoulos and Newcomb, 2020). Two maternally deposited morphogens, Bcd and Dl, are key factors that orchestrate this patterning process.…”
Section: Introductionmentioning
confidence: 99%
“…To determine the extent of MBT in our cell cycle-arrested embryos, we examined postcellularization development. Precisely orchestrated zygotic transcriptional networks subdivide the body plan into segments and guide gastrulation [15,31,45]. As part of this program, many transcriptional inputs guide engrailed gene expression in segmentally repeated stripes [46,47].…”
Section: Gastrulation and Embryonic Patterning In Cell Cycle-arrestedmentioning
confidence: 99%
“…The occurrence of post-MBT developmental events implied the activation of zygotic gene expression, but these studies did not indicate the extent of this activation. To gain a full picture of the dynamics of the transcriptome after cessation of the rapid early cycles, we manually collected embryos that were arrested in cycle 12 (C12) with triple cyclin RNAi for different amounts of time (15,30,50, and 70 minutes after completion of mitosis 11), as well as control embryos at different cell cycles, and carried out single-embryo RNA-seq analyses (Fig 3A and S1 Table). We calculated the Log 2 -transformed count per million (Log 2 CPM+1) for each gene (S2 Table) to allow comparison of their expression levels among different embryos.…”
Section: Transcriptome Dynamics Of the Embryos Arrested In Cycle 12mentioning
confidence: 99%
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