They learn more if instead it emits an alpha particle (two protons and two neutrons) to produce a «
daughter nucleus» and then that emits another alpha and so on.
Fragments that fail to segregate to
daughter nuclei form micronuclei, resulting in an unstable genome and cancer.
Not exact matches
Either the mother and
daughter succeed in stretching the tether to its breaking point, or they give up in the tug - of - war and revert to being a single cell with two
nuclei.
Accommodating these extra structures into the
daughter cell's
nucleus might be what increases the overall cell size.
In the center, FGFR - TACC fusion protein (red) can be seen disrupting tubulin bundles (green), structures that support cell division, or mitosis, at the point connecting the two
daughter cells (whose
nuclei are colored blue).
Here, FGFR - TACC (shown in red) can be seen interacting with tubulin bundles (green), structures that support mitosis, at the point connecting the two
daughter cells (whose
nuclei are colored blue).
A careful analysis allows us to track
nuclei movements over time, to determine when cell divisions occur, to measure the orientation of
daughter cells in three dimensions and to generate the complete lineage of all cells (von Wangenheim et al. 2014; Rosquete et al. 2013; Lucas et al. 2013; Vermeer et al. 2014).
This picture shows the
nucleus of one of two new
daughter cells.