Describe the structure of DNA, including complementary base pairing, and summarize the key experiments that revealed it.
The case that DNA is the molecule of heredity was built in pieces. In 1928, Frederick Griffith found that harmless bacteria could be permanently "transformed" into a dangerous strain just by exposure to remains of dead dangerous bacteria, showing some "transforming factor" could pass genetic information between organisms. In 1944, Avery, MacLeod, and McCarty identified that transforming factor specifically as DNA, not protein. Erwin Chargaff then discovered a striking pattern: in any organism's DNA, the amount of adenine always equals the amount of thymine, and the amount of guanine always equals the amount of cytosine. The final structural piece came from Rosalind Franklin's X-ray diffraction images of DNA fibers, especially the image known as Photo 51, which revealed a regular, measurable helical pattern; James Watson and Francis Crick combined Franklin's essential structural data with Chargaff's ratios to build the double-helix model in 1953.
DNA's monomer is the nucleotide: a deoxyribose sugar, a phosphate group, and one of four nitrogen bases (adenine, thymine, guanine, or cytosine). Two strands of nucleotides run in opposite directions (antiparallel), joined by a sugar-phosphate backbone on the outside, with bases paired in the middle by hydrogen bonds according to a strict complementary rule: adenine always pairs with thymine (two hydrogen bonds), and guanine always pairs with cytosine (three hydrogen bonds) -- exactly the mechanism behind Chargaff's ratios, now explained rather than just observed.
Mastery looks like: They can build a complementary, antiparallel DNA strand from a given sequence, apply Chargaff's rule, and summarize the key experimental evidence behind the double-helix model.
Common stumbles: Pairing bases without reversing the strand direction (forgetting "antiparallel"); mixing up which base pairs with which.