Schematic of the FISH assays used by Hirsch et al1 to assess chromosomal aneuploidy and allelic replication timing. Interphase FISH (bottom left) demonstrates the expected patterns for diploid and monosomy 7 cells using probes for chromosomes 8 (yellow) and 7 (magenta). The expected hybridization pattern for replication synchronous alleles using a single yellow probe will differ depending on where the cells are in cycle (bottom right). Postmitotic cells in G1 and early S phase (before replication) will exhibit a “singlet-singlet” signal corresponding to each allele, while cells that have undergone replication later in S phase will exhibit a “doublet-doublet” pattern corresponding to the 2 replicated alleles. Professional illustration by Marie Dauenheimer.

Schematic of the FISH assays used by Hirsch et al to assess chromosomal aneuploidy and allelic replication timing. Interphase FISH (bottom left) demonstrates the expected patterns for diploid and monosomy 7 cells using probes for chromosomes 8 (yellow) and 7 (magenta). The expected hybridization pattern for replication synchronous alleles using a single yellow probe will differ depending on where the cells are in cycle (bottom right). Postmitotic cells in G1 and early S phase (before replication) will exhibit a “singlet-singlet” signal corresponding to each allele, while cells that have undergone replication later in S phase will exhibit a “doublet-doublet” pattern corresponding to the 2 replicated alleles. Professional illustration by Marie Dauenheimer.

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