3D Genetic Structure in Blood Cancer Important Beyond DNA Code Changes
Retrieved on:
Monday, March 23, 2020
Upon receiving the right signal, this arrangement changes to expose the gene-reading machinery to only those bits of DNA code needed for the job at hand in each cell.
Key Points:
- Upon receiving the right signal, this arrangement changes to expose the gene-reading machinery to only those bits of DNA code needed for the job at hand in each cell.
- Within TAD boundaries, DNA is free to fold back on itself in 3D loops, bringing together enhancers and other elements (e.g., promoter DNA) that must interact for a given stretch of code to be read.
- Researchers say their findings suggest that these 3D changes in chromosome structure are as important as changes in the order of molecular letters making up the DNA code itself (mutations), with both mechanisms encouraging cancer onset and progress.
- However, a second experimental drug (targeting molecular, or epigenetic, changes in these DNA neighborhoods) effectively corrected DNA looping in the MYC neighborhood, restoring normal chromosomal structure and gene regulation, and dramatically decreasing MYC action and cancer spread.