36 research outputs found
STAT Is an Essential Activator of the Zygotic Genome in the Early Drosophila Embryo
In many organisms, transcription of the zygotic genome begins during the
maternal-to-zygotic transition (MZT), which is characterized by a dramatic
increase in global transcriptional activities and coincides with embryonic stem
cell differentiation. In Drosophila, it has been shown that
maternal morphogen gradients and ubiquitously distributed general transcription
factors may cooperate to upregulate zygotic genes that are essential for pattern
formation in the early embryo. Here, we show that Drosophila
STAT (STAT92E) functions as a general transcription factor that, together with
the transcription factor Zelda, induces transcription of a large number of
early-transcribed zygotic genes during the MZT. STAT92E is present in the early
embryo as a maternal product and is active around the MZT. DNA–binding
motifs for STAT and Zelda are highly enriched in promoters of early zygotic
genes but not in housekeeping genes. Loss of Stat92E in the
early embryo, similarly to loss of zelda, preferentially
down-regulates early zygotic genes important for pattern formation. We further
show that STAT92E and Zelda synergistically regulate transcription. We conclude
that STAT92E, in conjunction with Zelda, plays an important role in
transcription of the zygotic genome at the onset of embryonic development
Tempo and Mode in Evolution of Transcriptional Regulation
Perennial questions of evolutionary biology can be applied to gene regulatory systems using the abundance of experimental data addressing gene regulation in a comparative context. What is the tempo (frequency, rate) and mode (way, mechanism) of transcriptional regulatory evolution? Here we synthesize the results of 230 experiments performed on insects and nematodes in which regulatory DNA from one species was used to drive gene expression in another species. General principles of regulatory evolution emerge. Gene regulatory evolution is widespread and accumulates with genetic divergence in both insects and nematodes. Divergence in cis is more common than divergence in trans. Coevolution between cis and trans shows a particular increase over greater evolutionary timespans, especially in sex-specific gene regulation. Despite these generalities, the evolution of gene regulation is gene- and taxon-specific. The congruence of these conclusions with evidence from other types of experiments suggests that general principles are discoverable, and a unified view of the tempo and mode of regulatory evolution may be achievable
Cleavage modification did not alter blastomere fates during bryozoan evolution
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 study was funded by the core budget of the Sars Centre and by The
European Research Council Community’s Framework Program Horizon 2020
(2014–2020) ERC grant agreement 648861 to A
Coordinated Post-Transcriptional Regulation of the Chemokine System: Messages from CCL2
The molecular cross-talk between epithelium and immune cells in the airway mucosa is a key regulator of homeostatic immune surveillance and is crucially involved in the development of chronic lung inflammatory diseases. The patterns of gene expression that follow the sensitization process occurring in allergic asthma and chronic rhinosinusitis and those present in the neutrophilic response of other chronic inflammatory lung diseases such as chronic obstructive pulmonary disease (COPD) are tightly regulated in their specificity. Studies exploring the global transcript profiles associated with determinants of post-transcriptional gene regulation (PTR) such as RNA-binding proteins (RBP) and microRNAs identified several of these factors as being crucially involved in controlling the expression of chemokines upon airway epithelial cell stimulation with cytokines prototypic of Th1- or Th2-driven responses. These studies also uncovered the participation of these pathways to glucocorticoids' inhibitory effect on the epithelial chemokine network. Unmasking the molecular mechanisms of chemokine PTR may likely uncover novel therapeutic strategies for the blockade of proinflammatory pathways that are pathogenetic for asthma, COPD, and other lung inflammatory diseases