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01 // DOUBLE HELIX

GENOME.

DNA consists of two complementary strands that twist into a double helix. The sequence of bases — adenine, thymine, cytosine, and guanine — carries biological information.

MOLECULES / HELIX A · T · C · G
02 // NITROGENOUS BASES

A — T / C — G

Adenine pairs with thymine, while cytosine pairs with guanine. In DNA, adenine and thymine are connected by two hydrogen bonds, whereas cytosine and guanine are connected by three.

CURSOR → GENTLE MOLECULAR DISPLACEMENT
03 // DNA BACKBONE

SUGAR + PHOSPHATE

Each DNA strand has a backbone made of alternating deoxyribose and phosphate molecules. Attached to the sugar is one of four nitrogenous bases: A, T, C, or G.

DEOXYRIBOSE / PHOSPHATE / BASE
04 // GENOME SCALE

3 BILLION PAIRS

A single copy of the human genome contains approximately 3 billion DNA base pairs, distributed across 23 chromosomes. It is the sequence of these bases that forms the genome's record.

05 // DNA IN THE CELL CHROMATIN / HISTONES
DNA PACKAGING

FITTING DNA INSIDE THE NUCLEUS.

If the DNA from a single human cell were stretched out and laid in a straight line, it would be about 1.8 meters long. Histones and nucleosomes help package it inside the nucleus.

FILM / 05

About 150 DNA base pairs wrap around a core of histone proteins, forming a nucleosome — the basic unit of chromatin packaging.

06 // CHROMOSOMES
01

23 pairs of chromosomes. 46 chromosomes in most body cells.

Humans have 22 pairs of autosomes and one pair of sex chromosomes. One chromosome from each pair is inherited from one parent, and the other from the other parent.

07 // GENES

ABOUT 20,000 GENES

The human genome contains about 20,000 protein-coding genes. A gene is a segment of DNA containing the information a cell needs to produce a biological product, often a protein or RNA molecule.

01 GENE / INFORMATION

CODING

A DNA sequence can contain instructions for protein synthesis. The cell first transcribes the information from DNA into RNA and then uses it during protein synthesis.

08 // SIMILARITIES AND DIFFERENCES
99.6%

SHARED CODE

On average, about 99.6% of the human genome sequence agrees with the reference genome when different types of genetic variants are taken into account. A small fraction of differences creates enormous diversity among people.

FACTS ABOUT THE HUMAN GENOME ↗
23 pairs of chromosomes in most body cells
3 bn approximately base pairs in one copy of the genome
20,000 approximately genes in the human genome
99.6% average genome similarity to the reference sequence