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Borjigin, T.

Publications and source records attributed to Borjigin, T..

3 recordsLinked to original sources

Multiscale spatial analysis implicates chromosomal metaloops in gene patterning across the Drosophila brain

Scores of chromosome-scale loops, or metaloops, arise in the Drosophila brain, but their spatial organization and relationship to neural gene expression patterns remain unclear. Here, we used multiplexed Optical Reconstruction of Chromatin Architecture (ORCA) to examine the multiscale spatial organization of metaloops in cross-sections of 100s of larval and adult Drosophila brains. We find metaloops form preferentially in the central regions of the brain, where they nucleate the formation of metadomains, characterized by the intermingling of distal topologically associating domains (TADs). At the sub-cellular scale, metaloops tend to arise towards the nuclear center, and multiple metaloops in the same cell have a preference to form hubs (3 or more contacts). Each brain nucleus generally harbors only a few loops or hubs. An in-depth analysis of the hub centered on DIP-epsilon, a synaptic wiring gene, identified a three-way metadomain that brings together the DIP-epsilon TAD; a distal TAD carrying a paralog of DIP-epsilon, DIP-zeta; and a putative regulatory TAD, across 3 Mb. This metadomain adopts distinct conformations depending on gene expression; cells expressing DIP-epsilon or DIP-zeta show preferential interactions between the TAD carrying the corresponding gene and the putative regulatory TAD. We posit that the neuron-specific formation of different subsets of metadomains might coordinate the expression of diverse combinations of synaptic wiring genes underlying complex brain architecture.

molecular biology↗

Loop Extrusion Accelerates Long-Range Enhancer-Promoter Searches in Living Embryos

Long-range gene regulation underlies a variety of human developmental disorders including Cornelia de Lange syndrome1 and polydactyly2. Cohesin-mediated loop extrusion and tether-like elements are two major mechanisms implicated in fostering long-range enhancer-promoter (E-P) contacts3. However, our understanding of the contributions of these mechanisms to the kinetics of E-P interactions is limited. Here we employ a combination of quantitative single-cell imaging, genetic manipulations and polymer simulations to examine the interplay of cohesin-mediated loop extrusion and tethering elements4,5 in the timely activation of gene expression in living Drosophila embryos. Depletion of NIPBL or deletion of an enhancer-proximal CTCF anchor element reduced expression without changing the duration of individual transcriptional bursts. Genetic epistasis experiments recapitulated polymer simulations predicting complementation of tether deletions by augmenting the stability of cohesin via reduced levels of WAPL6. We propose a "scan and snag" model whereby directional cohesin-driven enhancer scanning promotes diffusion-mediated tethering interactions to produce successful E-P contacts and transcriptional activation. We discuss how modulating cohesin stability and the "stickiness" of looping factors7-10 can fine-tune the levels and timing of gene expression in mammalian developmental and disease processes.

molecular biology↗

Comprehensive Single Molecule View of Transcriptional Dynamics in Development

Dynamic patterns of gene expression drive animal development. These transcriptional dynamics depend on the interplay of diverse developmental enhancers within complex regulatory landscapes. Here, we employ a single-molecule genomic method, Fiber-Seq, to capture the simultaneous transcriptional and regulatory states of millions of 20-30 kb chromatin fibers in the 2-4hr Drosophila embryo. These snapshots of genes and their surrounding regulatory context reveal that the basic unit of transcription at highly transcribed genes is a convoy of 2-14 tightly spaced polymerases (Pol II). Further, a subset of templates exhibits hyperbursting, whereby most or all nucleosomes are evicted from the gene body facilitating maximum rates of transcription. We demonstrate that hyperbursting is achieved through cooperation of numerous cis-regulatory elements, and that the resulting nucleosome eviction appears to trigger a novel silencer in the ftz 3 UTR. We anticipate that similar mechanisms are used by vertebrate processes requiring intense transcription like somitogenesis and erythropoiesis.

developmental biology↗