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Julien, E.

Publications and source records attributed to Julien, E..

3 recordsLinked to original sources

Isotype specific loss of HP1α but not of HP1β uncovers genomic regions that behave as HP1α-dependent common fragile sites

HP1 proteins are highly evolutionarily conserved chromatin-associated factors known to play essential roles in genome stability and nuclear organization. In mammals, three HP1 isoforms, HP1, HP1{beta} and HP1{gamma}, have been described, but their individual functions remain incompletely characterized. Here, we inactivated HP1 or HP1{beta} in different cell lines and quantified chromosomal breaks on metaphase spreads in the presence or absence of aphidicolin-induced replication stress. Loss of HP1, but not of HP1{beta}, led to a significant increase of chromosomal breaks on chromosome arms and within pericentromeric heterochromatin under these conditions. Mechanistically, loss of HP1 was associated with a reduction in replication fork velocity, suggesting that HP1 deficiency induces a replication stress that sensitizes specific genomic loci to replication perturbation. Consistent with this, HP1 loss was associated with a moderate but consistent increase in {gamma}H2AX and 53BP1 foci, an increased occurrence of DNA synthesis during mitosis, and enhanced recruitment of FANCD2, all recognized as hallmarks of common fragile site (CFS) expression. In addition, rescue experiments using a chromodomain mutant HP1 (V22M) unable to bind H3K9me3 indicated that HP1 protective function over these specific foci did not require its interaction with this histone mark. Altogether, these data indicate that, independently of its binding to H3K9me3, HP1 stabilizes specific genomic regions that behave as HP1-dependent fragile sites, at least in part by regulating replication fork progression, limiting mitotic DNA synthesis possibly by competing with FANCD2 for chromatin access at these regions.

cell biology↗

Robust Organ Shape During Growth Requires Local Morphogen Signaling and Global Curvature Feedback

Precise organ shape during development requires feedback between organ-scale geometry and cell-level growth dynamics. Here, we use the apical hook of dicotyledonous plants as a model to study this multiscale control. This protective structure forms a [~]180{degrees} bend that is stably maintained despite rapid elongation. Combining quantitative growth mapping, multiscale modeling, and hormone analysis, we identify the cellular dynamics underlying hook maintenance. Contrary to the prevailing model, hook stability does not arise from sustained inner-outer growth asymmetry. Instead, stable curvature emerges from a biphasic, self-similar growth pattern that remains spatially fixed despite continuous cell flux. Auxin-driven growth asymmetry induces bending but is spatially restricted and insufficient to maintain shape. By contrast, a graded, auxin-independent autotropic response provides curvature-dependent growth regulation that counteracts bending and stabilizes shape against perturbations. Together, these findings establish a general principle in which local morphogen-driven bending and global geometry-dependent feedback jointly maintain robust organ shape during growth. HighlightsO_LISelf-similar growth maintains apical hook curvature despite continuous cell flux C_LIO_LICurvature stability emerges from coordinated axial and differential growth C_LIO_LIAuxin asymmetry is spatially restricted and insufficient for shape maintenance C_LIO_LICurvature-dependent feedback ensures robust and optimized hook shape C_LI

plant biology↗

A histone H4K20 methylation-mediated chromatin compaction threshold ensures genome integrity by limiting DNA replication licensing

The decompaction and re-establishment of chromatin organization immediately after mitosis is essential for genome regulation. The mechanisms underlying chromatin structure control in daughter cells are not fully understood. Here, we show that a chromatin compaction threshold in cells exiting mitosis ensures genome integrity by limiting replication licensing in G1 phase. Upon mitotic exit, appropriate chromatin relaxation is safeguarded by SET8-dependent methylation of histone H4 on lysine 20. Thus, in the absence of either SET8 or the H4K20 residue, substantial genome-wide chromatin decompaction occurs which allows excessive loading of the Origin Recognition Complex (ORC) in the daughter cells. ORC overloading stimulates aberrant recruitment of the MCM2-7 complex that promotes single-stranded DNA formation and DNA damage. Restoring chromatin compaction restrains excess replication licensing and the loss of genome integrity. Our findings identify a cell cycle-specific mechanism whereby fine-tuned chromatin relaxation suppresses excessive detrimental replication licensing and maintains genome integrity at the cellular transition from mitosis to G1 phase.

molecular biology↗