The researchers reported that TBK1 directly binds to and activates two proteins called CEP170 and NuMA that are involved in the separation of
chromosomes during mitosis.
After the parental cell DNA is replicated, the duplicated DNA and cellular organelles are separated into two daughter
cells during mitosis.
We are using these systems to explore the mechanisms that control spindle
orientation during mitosis, epithelial homeostasis, and multipotency versus unipotency in mammary stem cells.
Condensin in turn tethers these highly active genes to centromeres, such that they are protected and faithfully
segregated during mitosis.
His first renderings of chromosomes
separating during mitosis weren't much more sophisticated than his earlier plasticine worms.
Simple genetic mutations that take
place during mitosis can also cause a discrepancy in DNA test comparisons.
Meiosis uses many of the same biochemical mechanisms
employed during mitosis to accomplish the redistribution of chromosomes.
Next, they modified the repair proteins in order to impose DNA
repair during mitosis, and watched what happened.
This revealed telomeres as dangerous
structures during mitosis, because the cells momentarily lost the ability to distinguish between damaged DNA strands and normal telomeres.
They discovered that TBK1 is modified by addition of phosphate
groups during mitosis and TBK1 localizes to regions of the cell called centrosomes that regulate chromosomal separation.
When imposing repair on broken DNA
strands during mitosis, some telomeres are seen to fuse together (one dot).
«A way to stabilize haploidy in animal cells: Mammalian haploid cells present
problems during mitosis that limit their viability; the removal of the p53 tumor suppressor gene increases the survival rate of these cells thereby stabilising their haploid state.»
During the mitosis stage of budding yeast's division, aggregates of abnormal protein are tethered to well - anchored mitochondria in the mother cell.
In roughly one - quarter of dividing human cells observed by Tomomi Kiyomitsu, a postdoctoral researcher in Whitehead Institute Member Iain Cheeseman's lab, the spindle was
misaligned during mitosis, even after the paired chromosomes were pulled to opposite sides of the cell in late anaphase.
In humans, aneuploidy is well known to be deleterious, causing genetic disorders such as Down syndrome (trisomy 21), and frequently
occurring during mitosis in the genesis of cancer.
The reason for the rapid development of resistance was that these fungicides were single site inhibitors of fungal microtubule
assembly during mitosis, via tubulin - benzimidazole - interactions.
Remarkably, individual chromosomes remain separate
entities during mitosis, whereas many other polymeric assemblies fuse with each other upon contact in a liquid - like manner.
The main focus of our research is to understand the regulation of gene expression by cohesin and related proteins, which are also required for sister chromatid
cohesion during mitosis (see «Background»).
Until now, however, none has actually seen how human cells manage to divide into two equally - sized daughter
cells during mitosis.
Finally, as we and others have shown, errors in chromosome
segregation during mitosis have dramatic secondary consequences on genome integrity, including translocations, deletions and chromosome shattering (chromothripsis).
We found that the interaction between two classic factors, condensin and TBP, plays a pivotal role in 3D chromosome organization, and ensures that a critical set of genes, the actively transcribed housekeeping genes, are accurately
segregated during mitosis (Figure B and C).
During mitosis, microtubules disassemble and reform into spindles that are used by the dividing cell to move chromosomes.
Their studies show that the problem arises when the haploid cells try to separate their chromosomes
during mitosis.
Heritable genetic variation is the result of genome instability during germ cell development, instability that arises through mutation, chromosome rearrangement or chromosome mis - segregation
during mitosis or meiosis.
Until now, however, none has actually seen how cells manage to divide precisely into two equally - sized daughter cells
during mitosis.
During mitosis, they contribute to the formation and orientation of the mitotic spindle.
Present at highest level in G2 phase and
during mitosis (at protein level).
Splitting of centriole pairs in primary cells leads to multipolar spindles and causes mis - segregation of chromosomes
during mitosis (aneuploidy).