The finding suggests that cells can use their existing molecular machinery to handle synthetic genetic information. That marks an important step toward a long-standing goal in synthetic biology: expanding the language of DNA beyond the four letters found in nature. In the future, such systems could help scientists engineer biological machinery that carries out new functions or produces compounds that do not naturally exist.

How Cells Read an Eight-Letter Genetic Alphabet

The researchers focused on RNA polymerase, the enzyme that reads DNA and produces RNA -- the first step in gene expression. To see how the enzyme handles synthetic genetic information, the team combined biochemical experiments with high-resolution cryo-electron microscopy capable of revealing structures at scales smaller than the width of a single atom.

The researchers captured detailed structural views of RNA polymerase from Escherichia coli (E. coli) bacteria as it recognized and incorporated two synthetic base pairs. These artificial genetic letters are not found in nature.

The images showed that RNA polymerase identifies the synthetic DNA letters using many of the same biochemical and structural signals it relies on to recognize natural base pairs. That finding helps explain why the enzyme can accurately copy information written using an expanded genetic alphabet.

In a related study published in PNAS, the same research team found that RNA polymerase can also recognize another pair of synthetic base pairs even though they lack the hydrogen bonds that normally help hold DNA base pairs together.

Synthetic DNA Could Enable New Technologies

The potential applications extend well beyond understanding how DNA works. Earlier research has already used expanded genetic alphabets to create synthetic DNA molecules capable of recognizing liver cancer cells.

By showing in molecular detail how RNA polymerase reads and transcribes non-natural DNA letters, the new research provides an important foundation for technologies built around expanded genetic codes. Possible applications include new diagnostic tools, therapeutics, and engineered biological systems with capabilities that do not occur naturally.

Two Studies Explore Expanded Genetic Codes

The Nature Communications study ("Structural Basis of Transcription of the Hachimoji Eight-Letter Alphabet by E. coli RNA Polymerase"), led by Dong Wang, PhD, professor at the UC San Diego Skaggs School of Pharmacy and Pharmaceutical Sciences, was published on Sept. 2, 2026 in Nature Communications.

The PNAS study ("Hydrophobic unnatural base pair promotes trigger loop closure and catalysis in cellular RNA polymerase independent of hydrogen bonding"), published on Aug. 12, 2026, was also led by Wang.