17 research outputs found
Common bursting relationships underlie eukaryotic transcription dynamics
Transcription commonly occurs in bursts resulting from alternating productive
(ON) and quiescent (OFF) periods. Yet how transcriptional bursts are regulated
to determine spatiotemporal transcriptional activity remains unclear. Here we
perform live transcription imaging of key developmental genes in the fly
embryo, with single polymerase sensitivity. Quantification of single allele
transcription rates and multi-polymerase bursts reveals shared bursting
relationships among all genes, across time and space, as well as cis- and
trans-perturbations. We identify the allele's ON-probability as the main
determinant of the transcription rate, while changes in the transcription
initiation rate are limited. Any given ON-probability determines a specific
combination of mean ON and OFF times, preserving a constant characteristic
bursting time scale. Our findings point to a convergence of various regulatory
processes that predominantly affect the ON-probability, thereby controlling
mRNA production rather than mechanism-specific modulation of ON and OFF times.
Our results thus motivate and guide new investigations into the mechanisms
implementing these bursting rules and governing transcriptional regulation
Transient transcriptional responses to stress are generated by opposing effects of mRNA production and degradation
The state of the transcriptome reflects a balance between mRNA production and degradation. Yet how these two regulatory arms interact in shaping the kinetics of the transcriptome in response to environmental changes is not known. We subjected yeast to two stresses, one that induces a fast and transient response, and another that triggers a slow enduring response. We then used microarrays following transcriptional arrest to measure genome-wide decay profiles under each condition. We found condition-specific changes in mRNA decay rates and coordination between mRNA production and degradation. In the transient response, most induced genes were surprisingly destabilized, whereas repressed genes were somewhat stabilized, exhibiting counteraction between production and degradation. This strategy can reconcile high steady-state level with short response time among induced genes. In contrast, the stress that induces the slow response displays the more expected behavior, whereby most induced genes are stabilized, and repressed genes are destabilized. Our results show genome-wide interplay between mRNA production and degradation, and that alternative modes of such interplay determine the kinetics of the transcriptome in response to stress
Functional analysis of the Drosophila eve locus in response to non-canonical combinations of gap gene expression levels
International audienceTranscription factor combinations play a key role in shaping cellular identity. However, the precise relationship between specific combinations and downstream effects remains elusive. Here, we investigate this relationship within the context of the Drosophila eve locus, which is controlled by gap genes. We measure spatiotemporal levels of four gap genes in heterozygous and homozygous gap mutant embryos and correlate them with the striped eve activity pattern. Although changes in gap gene expression extend beyond the manipulated gene, the spatial patterns of Eve expression closely mirror canonical activation levels in wild type. Interestingly, some combinations deviate from the wild-type repertoire but still drive eve activation. Although in homozygous mutants some Eve stripes exhibit partial penetrance, stripes consistently emerge at reproducible positions, even with varying gap gene levels. Our findings suggest a robust molecular canalization of cell fates in gap mutants and provide insights into the regulatory constraints governing multi-enhancer gene loci
Common bursting relationships underlie eukaryotic transcription dynamics
Transcription commonly occurs in bursts resulting from alternating productive (ON) and quiescent (OFF) periods. Yet how transcriptional bursts are regulated to determine spatiotemporal transcriptional activity remains unclear. Here we perform live transcription imaging of key developmental genes in the fly embryo, with single polymerase sensitivity. Quantification of single allele transcription rates and multi-polymerase bursts reveals shared bursting relationships among all genes, across time and space, as well as cis-and trans-perturbations. We identify the allele's ON-probability as the main determinant of the transcription rate, while changes in the transcription initiation rate are limited. Any given ON-probability determines a specific combination of mean ON and OFF times, preserving a constant characteristic bursting time scale. Our findings point to a convergence of various regulatory processes that predominantly affect the ON-probability, thereby controlling mRNA production rather than mechanism-specific modulation of ON and OFF times. Our results thus motivate and guide new investigations into the mechanisms implementing these bursting rules and governing transcriptional regulation
Dynamic interplay between enhancer–promoter topology and gene activity
International audienc
Transcriptional coupling of distant regulatory genes in living embryos
International audienceThe prevailing view of metazoan gene regulation is that individual genes are independently regulated by their own dedicated sets of transcriptional enhancers. Past studies have reported long-range gene–gene associations1,2,3, but their functional importance in regulating transcription remains unclear. Here we used quantitative single-cell live imaging methods to provide a demonstration of co-dependent transcriptional dynamics of genes separated by large genomic distances in living Drosophila embryos. We find extensive physical and functional associations of distant paralogous genes, including co-regulation by shared enhancers and co-transcriptional initiation over distances of nearly 250 kilobases. Regulatory interconnectivity depends on promoter-proximal tethering elements, and perturbations in these elements uncouple transcription and alter the bursting dynamics of distant genes, suggesting a role of genome topology in the formation and stability of co-transcriptional hubs. Transcriptional coupling is detected throughout the fly genome and encompasses a broad spectrum of conserved developmental processes, suggesting a general strategy for long-range integration of gene activity