Q.Write a short note on DNA packaging in a eukaryotic cell.
Eukaryotic DNA is compacted by wrapping around histone octamers to form nucleosomes, which coil into a 30 nm solenoid and then supercoil further into loops and the fully condensed metaphase chromosome.
Step 1. The basic packaging unit is the nucleosome: a histone octamer (two molecules each of H2A, H2B, H3 and H4) around which about 200 bp of the negatively charged DNA helix is wrapped, roughly 146 bp wound about 1(3/4) turns around the octamer, with the remainder acting as linker DNA; histone H1 binds where the DNA enters and leaves each nucleosome.
Step 2. Under the electron microscope, a chain of nucleosomes joined by linker DNA looks like 'beads on a string' -- the first level of chromatin compaction (about 10-11 nm thick).
Step 3. About six nucleosomes coil together into a helical, 30 nm-thick solenoid structure, resembling a coiled telephone wire.
Step 4. The solenoid fibre supercoils further into looped domains, and with the help of additional Non-Histone Chromosomal (NHC) proteins, condenses progressively until it forms the fully compact chromosome visible at metaphase.
Eukaryotic DNA is packaged in stages -- nucleosome formation around histone octamers, beads-on-a-string chromatin, coiling into a 30 nm solenoid, and further NHC-protein-assisted supercoiling and looping -- culminating in the condensed metaphase chromosome.
Unlock everything free for 14 days
- Full step-by-step solutions
- Concept-first explanations
- Methods, shortcuts & mistakes
- PYQ mapping + timed mock tests
Full access for 14 days. No credit card required.