Needleman is especially interested in the spindle, a cellular structure that separates chromosomes and pulls the duplicated DNA from the mother
cell into the daughter cell during division.
But when the researchers used live microscopy to watch how the 4 - millimeter - wide organoids developed, they noticed that human progenitor cells took 50 % longer than those of the other great apes to arrange their chromosomes before
splitting into daughter cells.
These erratic, small extra nuclei, which contain fragments, or whole chromosomes that were not
incorporated into daughter cells after cell division, are associated with specific forms of cancer and are predictive of poorer prognosis.
«This suggests that cell division is used not only to transmit the genetic
information into daughter cells and create two equivalent cells,» he said, «but it is also an opportunity for cells to reorganize their genomes in 3D space, sequestering parts of the genome at the nuclear periphery and rendering it inaccessible to transcription.»
The efficient compaction of DNA during cellular division ensures equal distribution of
DNA into daughter cells and prevents aneuploidy, which has been implicated as a major driver of tumor development.
Furthermore, cells in which MELK had been depleted displayed asymmetric division (Figure 6G), characterized by an unequal allocation of cell
mass into daughter cells.
Spindles are cellular structures that play an important role in cell division, separating chromosomes and pulling the duplicated DNA from the mother
cell into the daughter cell.