Issue |
Med Sci (Paris)
Volume 21, Number 4, Avril 2005
|
|
---|---|---|
Page(s) | 371 - 376 | |
Section | M/S revues | |
DOI | https://doi.org/10.1051/medsci/2005214371 | |
Published online | 15 April 2005 |
L’épigénétique comme aspect de la postgénomique
Epigenetics as an aspect of post-genomics
Programme d’Épigénomique, Genopole ; ATelier de Génomique Cognitive (ATGC), CNRS UMR 8071/Genopole, 93, rue Henri-Rochefort, 91000 Évry, France
*
Francois.Kepes@genopole.cnrs.fr
Les modifications épigénétiques de l’activité des gènes usent de modalités très diverses pouvant toutefois se placer dans un référentiel unique fondé sur des échelles corrélées chimique, spatiale et temporelle. Ce référentiel permet d’intégrer les mutations purement génétiques à l’une de ses extrémités, autorisant ainsi une nouvelle vision graduelle allant du génome à l’épigénome au lieu de les opposer. À l’autre extrémité se trouvent deux sortes d’épimutations à grande portée spatiale, et rapides à produire un changement phénotypique : d’une part, des réarrangements de la structure tridimensionnelle du chromosome peuvent influencer l’expression génique de manière héritable ; ces réarrangements semblent eux-mêmes résulter de la dynamique collective des activités liées à l’ADN, en particulier transcriptionnelles. D’autre part, les états régulatoires héritables, par exemple une différenciation cellulaire résultant de la bascule d’un « interrupteur » régulatoire bistable, mettent en jeu des effecteurs distribués dans le noyau ou le cytoplasme, voire aux confins de la cellule.
Abstract
A cell transmits to its progeny the activity level of many of its genes, not just their sequence. Just like the sequence may vary through a mutation, the gene activity level may change through an « epimutation » (an epigenetic modification) which is heritable and does not entail any concomitant genetic alteration. An epimutation can have important phenotypic consequences, that eventually survive to the loss of the environmental conditions that triggered it. For instance, epimutations are responsible for the divergence between a neuron and an epithelial cell that both come from the same egg and contain the same genome complement. This phenotypic difference is much larger than the one between the neurons from two animal species with dissimilar genotypes, thereby underlining the importance of epimutations. Tradition opposes the genetic and epigenetic visions, the latter being often adequated to the DNA methylation phenomenon. However, epimutations display a rich spectrum of modes that can all fit in a unique reference system based on correlated chemical, spatial and temporal scales. This reference system allows the integration of purely genetic mutations at one of its ends, thus paving the way to a new, gradual vision that encompasses the genome and the epigenome. At the other end can be found two types of epimutations that are both wide-ranging in space and rapid in producing phenotypic alterations. Firstly, long-range rearrangements of the three-dimensional structure of the chromosome may influence gene expression in an heritable fashion. Such rearrangements seem to result from the collective dynamics of DNA-related activities, particularly transcription. Lastly, heritable regulatory states, e.g. a differentiated state that results from tipping a regulatory « toggle switch », involve components that are distributed throughout the nucleus or the cytoplasm, and possibly all the way to cell confines.
© 2005 médecine/sciences - Inserm / SRMS
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