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Mélody Merle

Publications and source records attributed to Mélody Merle.

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The 3D genome shapes the regulatory code of developmental genes

We revisit the notion of gene regulatory code in embryonic development in the light of recent findings about genome spatial organisation. By analogy with the genetic code, we posit that the concept of code can only be used if the corresponding adaptor can clearly be identified. An adaptor is here defined as an intermediary physical entity mediating the correspondence between codewords and objects in a gratuitous and evolvable way. In the context of the gene regulatory code, the encoded objects are the gene expression levels, while the concentrations of specific transcription factors in the cell nucleus provide the codewords. The notion of code is meaningful in the absence of direct physicochemical relationships between the objects and the codewords, when the mediation by an adaptor is required. We propose that a plausible adaptor for this code is the gene domain, that is, the genome segment delimited by topological insulators and comprising the gene and its enhancer regulatory sequences. We review recent evidences, based on genome-wide chromosome conformation capture experiments, showing that preferential contact domains found in metazoan genomes are the physical traces of gene domains. Accordingly, genome 3D folding plays a direct role in shaping the developmental gene regulatory code.

q-bio.GN

Turing-like patterns in an asymmetric dynamic Ising model

To investigate novel aspects of pattern formation in spin systems, we use a mapping between reactive concentrations in a reaction-diffusion system and spin orientations in a dynamic multiple-spin Ising model. While pattern formation in Ising models always rely on infinite-range interactions, this mapping allows us to design an finite-range interactions Ising model that can produce patterns observed in reaction diffusion systems including Turing patterns with a tunable typical length scale. This model has asymmetric interactions and several spin types coexisting at a site. While we use the example of genetic regulation during embryo-genesis to build our model, it can be used to study the behavior of other complex systems of interacting agents.

nlin.AO