Showing posts with label Cell Development. Show all posts
Showing posts with label Cell Development. Show all posts

Sunday, November 26, 2023

Cell Division: A Proposed Model for Cell Identity Preservation

While all cells in the human body contain the same DNA (genetic instructions), each cell expresses only the genes needed to become the cell type it is (i.e. neuron, lymphocyte, cardiomyocytes). Each cell’s fate is largely determined by chemical modifications to the histone proteins around the DNA, which control gene expression. Considering that these cells lose half of their modifications when replicating in cell division, a new MIT study suggests that these cells maintain their memory of what cell type they’re supposed to be through the 3D folding pattern of its genome determining which portions will be marked by chemical modifications. Essentially, the way that these chromosomes were folded are like a blueprint to determine where the remaining marks should go. Thus, by juggling between 3D folding and the marks, the epigenetic memory can be preserved over hundreds of divisions.


In general, this proposed model provides valuable insight into how epigenetic markings play a role in establishing cell identity and maintaining this memory after cell division. Through this model, biologists may be able to better understand how this epigenetic memory of cell identity is lost as cells begin to age and potentially better understand the epigenetic mechanisms underlying our genome.

For more information, view the news article linked here and the journal publication of the research study linked here.

Tuesday, April 7, 2015

Genetic clues on the origin of Hirschsprung's disease



Two genetic variations were found to cause Hirschsprung’s disease, a possibly fatal disease that occurs once in every five thousand births. Hirschsprung’s disease causes bowel obstruction in infants due to nerves that control the colon not developing properly in the womb. When left untreated Hirschsprung’s is fatal in infants.  Aravinda Chakravarti, a professor at Johns Hopkins University, started a study on the disease in 1990 and in 2002. In the studies 650 patients markers were compared. A variant in the Ret gene was found in common with the patients along with genes for several semaphorins, proteins that guide nerve cells growth. These two genes are part of a system of signals called pathways, and when the two variants are present the nerve cells that control the colon cannot develop.

Presently there are no tests to identify the likeliness of the disease. Hopefully with the information provided in this study there will be progress in developing a test to identify which children will be born with the disease, and treatment can be given immediately before fatalities can occur.