DNA 🧬 – The Cell’s Master Blueprint
DNA (deoxyribonucleic acid) is a super-long chain of deoxyribonucleotides. Scientists measure its length by simply counting the nucleotides (or base pairs). For instance, the tiny bacteriophage φ×174 carries 5 386 nucleotides, whereas a single human gamete contains 3.3 × 109 bp! :contentReference[oaicite:0]{index=0}
1. Building a Polynucleotide Chain 🔗
- 3 parts per nucleotide: a nitrogenous base, a pentose sugar (ribose or deoxyribose), and a phosphate group :contentReference[oaicite:1]{index=1}.
- Bases: Purines – Adenine (A) & Guanine (G); Pyrimidines – Cytosine (C), Thymine (T, in DNA) & Uracil (U, in RNA). Cytosine appears in both nucleic acids; U replaces T in RNA :contentReference[oaicite:2]{index=2}.
- A base joins the sugar’s 1′-OH by an N-glycosidic bond to form a nucleoside. Adding a phosphate to the sugar’s 5′-OH produces a nucleotide :contentReference[oaicite:3]{index=3}.
- Nucleotides link 3′→5′ through phosphodiester bonds, creating a chain with a free 5′-phosphate (the 5′ end) and a free 3′-OH (the 3′ end) :contentReference[oaicite:4]{index=4}.
- The sugar-phosphate “backbone” stays on the outside, while the bases stick in like steps of a ladder :contentReference[oaicite:5]{index=5}.
2. The Famous Double Helix 🌀
Watson and Crick—guided by Wilkins & Franklin’s X-ray images—designed the elegant double-helix model in 1953 :contentReference[oaicite:6]{index=6}. Key ideas:
- Two anti-parallel strands (one 5′→3′, the other 3′→5′) twist together :contentReference[oaicite:7]{index=7}.
- A pairs with T via 2 H-bonds; G pairs with C via 3 H-bonds, so a purine always meets a pyrimidine—keeping the helix width constant :contentReference[oaicite:8]{index=8}.
- Each turn holds roughly 10 bp, spans 3.4 nm, and successive base pairs sit 0.34 nm apart :contentReference[oaicite:9]{index=9}.
- Base pairs stack like coins, adding stability along with H-bonds :contentReference[oaicite:10]{index=10}.
Chargaff’s observation: In any double-stranded DNA, [A] = [T] and [G] = [C], so knowing one strand reveals its partner :contentReference[oaicite:11]{index=11}.
3. How Information Flows ➡️
Crick summarized it neatly as the Central Dogma: DNA → RNA → Protein :contentReference[oaicite:12]{index=12}. Some viruses run the arrow backwards (RNA → DNA) – a process we call reverse transcription 😯.
4. Fitting 2 meters of DNA into a Nucleus 📦
Multiply the human haploid DNA count by the rise per base pair to see the challenge:
\[ (6.6\times10^{9}\ \text{bp}) \times (0.34\times10^{-9}\ \text{m/bp}) \approx 2.2\ \text{m} \] :contentReference[oaicite:13]{index=13}
4.1 Prokaryotes 🦠
Bacteria lack a defined nucleus, yet DNA isn’t loose. Negative DNA loops attach to positively charged proteins in a central nucleoid area :contentReference[oaicite:14]{index=14}.
4.2 Eukaryotes 🧫
- Histone octamer: eight positively charged histone proteins (rich in lysine & arginine) :contentReference[oaicite:15]{index=15}.
- Nucleosome: ≈ 200 bp of DNA wrap 1.65 turns around the octamer—think “beads on a string” under the microscope :contentReference[oaicite:16]{index=16}.
- These beads coil into thicker chromatin fibers, then loop and fold to form visible chromosomes during mitosis :contentReference[oaicite:17]{index=17}.
- Loose, light-staining regions (euchromatin) stay transcription-ready; dense, dark regions (heterochromatin) remain largely silent :contentReference[oaicite:18]{index=18}.
- Extra “non-histone chromosomal” proteins guide the higher-order folding :contentReference[oaicite:19]{index=19}.
⭐ High-Yield NEET Nuggets
- Complementary base pairing & Chargaff’s rule – predict the opposite strand in seconds.
- Double-helix geometry – right-handed coil, 10 bp/turn, 0.34 nm rise; expect numbers-based questions.
- Central Dogma & reverse transcription – classic flow vs. viral detours.
- Nucleosome model – 200 bp per histone octamer, “beads-on-string” appearance.
- DNA length calculation & packaging – handy formula: bp × 0.34 nm gives the total length.
Keep exploring—DNA’s story just keeps getting twistier! 🎉