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Hickmann, C.

Publications and source records attributed to Hickmann, C..

2 recordsLinked to original sources

Outside-in progression of heterochromatin replication and exclusion of CDC45 from the PCH domain in Drosophila

Heterochromatin replication isnt random or uniform, but occurs in a characteristic spatial and temporal pattern. Previous studies produced conflicting models for pericentric heterochromatin (PCH) replication, suggesting either that heterochromatic sequences translocate to the domain surface for replication, or that replication can also occur internally through localized decondensation. To distinguish true overlap from peripheral enrichment around an irregular PCH domain, we developed FOC-Map, a colocalization analysis approach that combines segmentation of one channel with binning of the other. Applying FOC-Map to three-dimensional Airyscan imaging of cultured Drosophila cells, we find that replication foci at the onset of late S-phase are confined to the outer boundary of the PCH domain, forming a shell-like pattern with little overlap into the HP1a-rich interior. As late S-phase progresses, replication foci are observed within the domain, localizing to low-HP1a regions interspersed between more condensed regions. We then assessed the distribution of CDC45, a rate-limiting replication initiation factor, and found that CDC45 foci are depleted from the PCH domain throughout the cell cycle. We propose that low levels of CDC45 within HP1a-rich PCH limit replication initiation to the domain periphery, giving rise to the shell-like pattern of replication foci that progressively works inward until PCH replication is complete.

cell biology↗

Expanding the HP1a-binding consensus and molecular grammar for heterochromatin assembly

The recruitment of Heterochromatin Protein 1 (HP1) partners is essential for heterochromatin assembly and function, yet our knowledge regarding their organization in heterochromatin remains limited. Here we show that interactors engage the Drosophila HP1 (HP1a) dimer through a degenerate and expanded form of the previously identified PxVxL motif, which we now term HP1a Access Codes (HACs). These HACs reside in disordered regions, possess high conservation among Drosophila homologs, and contain alternating hydrophobic residues nested in a cluster of positively charged amino acids. These findings and molecular dynamics simulations identify key electrostatic interactions that modulate HP1a-binding strength and provide a dramatically improved HP1a-binding consensus motif that can reveal protein partners and the molecular grammar involved in heterochromatin assembly. We propose HP1a acts as a scaffold for other heterochromatin components containing HAC motifs, which in turn may regulate the function and higher order structure of the heterochromatin compartment.

molecular biology↗