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Biology subjects

Courtemanche, K.

Publications and source records attributed to Courtemanche, K..

2 recordsLinked to original sources

Cell-supracellular structural relations solve the French Flag Problem without graded molecular control

How patterns of cell state emerge across a tissue field is a fundamental question brought into renewed focus by spatial omics tools that map molecular states onto tissue organization. Here, we investigate how a field of limb progenitor mesenchyme transforms into distinct, adjacent cartilage and soft tissue compartments. We find that mesenchymal tissue fields self-organize their own differentiation through co-constitutive relationships between cell and supracellular structures, which produce cell-ECM or cell-cell-based supracellular cues that canalize cartilage or soft tissue cell fate change, respectively. At the tissue level, bifurcation in intrinsically generated supracellular structures guides the specification of tissue compartment size. We find that Wnt secreted from neighboring epithelial tissue influences mesenchymal cell fate and patterning by functioning as a modulator of cell-supracellular structural relations. Taken together, our results provide insight into how mesenchymal self-organization interfaces with epithelial signaling to enable a tissue compartmentalization process that initiates the skeleton.

developmental biology↗

The 9-1-1 complex protects ssDNA gaps in BRCA2-deficient cancer

Single-stranded DNA (ssDNA) gaps are a hallmark of BRCA-deficient cells, yet the mechanisms that safeguard these lesions remain unclear. Through a genome-wide CRISPR screen, we identified the RAD9A-HUS1-RAD1 (9-1-1) complex as essential for the survival of BRCA2-deficient cells through an ATR-independent mechanism. Loss of 9-1-1 in this context leads to the accumulation of PRIMPOL-dependent gaps that fail to undergo post-replicat ive repair, resulting in pathological expansion and increased DNA damage. This instability is driven by excessive EXO1-mediated degradation, as EXO1 depletion rescues the phenotype. We further demonstrate that the 9-1-1 complex is required for POL{zeta}-dependent gap filling. We propose a model in which ssDNA gaps, when extended beyond a critical length, become inaccessible to TLS-mediated repair and are fully reliant on homologous recombination. These findings establish the 9-1-1 complex as key regulator of ssDNA gap stability and a promising therapeutic target in BRCA2-deficient cancers. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=200 SRC="FIGDIR/small/680950v1_ufig1.gif" ALT="Figure 1"> View larger version (41K): org.highwire.dtl.DTLVardef@56516aorg.highwire.dtl.DTLVardef@fb1ce3org.highwire.dtl.DTLVardef@25a7b2org.highwire.dtl.DTLVardef@249731_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗