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This lesson introduces how and why we use ancient DNA analysis in archaeology, touching on the basics of the method and what it can show us. A quick note is required here to categorically state that sex is not the same as gender.

What is DNA?

DNA (deoxyribonucleic acid) forms the building blocks of living things. It is a kind of biological polymer that resides in the body as very large molecules, housed in the nuclei and mitochondria of our cells. We won’t delve into the depths of DNA and how it works in this introductory lesson, focusing instead on the bread and butter of DNA analysis in archaeology – base pairs, single-nucleotide polymorphisms, and investigating haplogroups.

The large molecules that DNA exist as take the form of a double helix; two long strands chained together in a twisting corkscrew shape. These strands are organised into chromosomes, which contain the majority of our genetic code and are copied into new cells the body creates. The two strands themselves are paired up with opposing nucleotides in the form of a base pair.

Nucleotides are composed of a deoxyribose (sugar), phosphate group, and a nucleotide base. These bases are guanine (G), cytosine (C), adenine (A), and thymine (T). Between the two strands of DNA these bases form a base pair, with guanine matching cytosine and adenine matching thymine. Thus a strand of DNA containing the sequence GAATTC would be paired with a strand containing CTTAAG.

These combinations of base pairs are genetic information, and are either coding or non-coding – although all are functional and valuable. Among other differences, coding sections provide some of the information necessary to create proteins while non-coding DNA does not. In archaeology, however, some of our most common DNA investigations are more interested in the sequence of DNA than what it actually does – it is this kind of investigation we are discussing here.

Figure 1. A DNA double helix showing base pairs (A–T and G–C), sugar-phosphate backbones, and strand direction (3′ to 5′).

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