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Baranasic, D.

Publications and source records attributed to Baranasic, D..

4 recordsLinked to original sources

Mapping non-coding functional elements in allotetraploid Cyprinus carpio embryo development reveals subgenome variation of transcription regulation

Common carp (Cyprinus carpio) is an important freshwater species for ornamental and aquaculture purposes, and a key cyprinid model for studying allotetraploidy. Its two chromosomally-separated subgenomes show distinct gene expression profiles, but how their regulatory landscapes control gene expression dynamics during development remains unknown. We generated a regulatory atlas by combining transcriptomes across 12 developmental stages with chromatin accessibility maps, transcription start sites and gene regulation-associated histone post-translational modifications. Subgenome-specific annotation and comparison of 254,276 developmental regulatory elements (PADREs) revealed that regulatory subgenome divergence is most prominent during early development, converging toward the phylotypic period, mirroring expression convergence between subgenomes at the same stages. This dynamic was driven by enhancers, while promoters maintained a more stable subgenome bias, extending the hourglass model of developmental constraint to allotetraploid subgenome regulation. Subgenome-specific enhancers were preferentially retained in subgenome B, whereas subgenome A shifted toward homeologous enhancer activity near the phylotypic stage, indicating directional regulatory divergence between subgenomes. Comparison with zebrafish revealed high concordance with sequence conservation and that subgenome B retained more ancestral cyprinid regulatory elements than subgenome A. This developmental regulatory atlas provides a foundational resource for investigating cis-regulatory evolution following the fourth round of vertebrate genome duplication.

genomics↗

Salmonids reveal principles of regulatory evolution following autotetraploidization

Early vertebrate autotetraploidization events may have enabled major innovations by expanding the genetic material for functional diversification, yet their ancient timing obscures how genome doubling reshaped gene regulatory evolution. Salmonids provide a unique window to these mechanisms, because they experienced a comparatively recent autotetraploidization and are earlier in the rediploidization process - which creates new genes and regulatory elements during evolution. Here, using large-scale multiomics spanning embryonic and adult tissues in two salmonids, we investigate gene regulatory evolution following genome doubling and rediploidization, which we show is governed by developmental and tissue-specific context, with a period of maximal constraint at advanced stages of embryogenesis. This work advances understanding of vertebrate genome evolution, while providing an open resource supporting salmonid aquaculture and conservation.

evolutionary biology↗

A dual enhancer-silencer element ensures transient Cdx2 expression during posterior body formation

During development, cells express precise gene expression programmes to assemble the trunk of the body plan. Appropriate control over the duration of the transcription factor Cdx2 is critical to achieve this outcome, yet, how cells control the onset, maintenance or termination of Cdx2, has remained unclear. Here, we delineate the cis-regulatory logic orchestrating dynamic Cdx2 expression in mouse caudal epiblast progenitors and their derivatives - spinal cord and presomitic mesoderm. Combining CRISPR-mediated deletion of regulatory elements with in vitro models and in vivo validation, we demonstrate that distinct enhancers, and a silencer, embedded at the Cdx2 locus, act sequentially to drive transient Cdx2 expression. We pinpoint a minimal silencer element that relies on a nuclear receptor motif to extinguish Cdx2. Changing this single motif converts the repressive element to an enhancer with opposite regulatory behaviour. Our findings elucidate design principles of developmental enhancers and silencers and establish a dual enhancer-silencer cis-regulatory logic ensuring precise spatiotemporal control over gene expression for vertebrate body patterning.

developmental biology↗

Integrative annotation of genomic features reveal functional elements and epigenetic landscapes in the developing zebrafish

Zebrafish, a popular model for embryonic development and for modelling human diseases, has so far lacked a systematic functional annotation programme akin to those in other animal models. To address this, we formed the international DANIO-CODE consortium and created the first central repository to store and process zebrafish developmental functional genomic data. Our Data Coordination Center (https://danio-code.zfin.org) combines a total of 1,802 sets of unpublished and reanalysed published genomics data, which we used to improve existing annotations and show its utility in experimental design. We identified over 140,000 cis-regulatory elements in development, including novel classes with distinct features dependent on their activity in time and space. We delineated the distinction between regulatory elements active during zygotic genome activation and those active during organogenesis, identifying new aspects of how they relate to each other. Finally, we matched regulatory elements and epigenomic landscapes between zebrafish and mouse and predict functional relationships between them beyond sequence similarity, extending the utility of zebrafish developmental genomics to mammals.

developmental biology↗