Nullomers

Nullomers are naturally available but potentially unused sequences of DNA. Determining these "forbidden" sequences can improve the understanding of the basic rules that govern sequence evolution.[4] Sequencing the entire genome has shown that there is a high level of non-uniformity in genomic sequences. When a codon is artificially substituted for a synonymous codon, it often results in a lethal change and cell death. This is believed to be due to ribosomal stalling and early termination of protein synthesis. For example, both AGA and CGA code for arginine in bacteria; however, bacteria almost never use AGA, and when substituted it proves lethal.[5] Such codon biases have been seen in all species,[6] and are examples of constraints on sequence evolution. Other sequences may have selective pressure; for example, GG-rich sequences are used as sacrificial sinks for oxidative damage because oxidizing agents are attracted to regions with GG-rich sequences and then induce strand breakage.[7] Moreover, it has been shown that statistically significant nullomers (i.e. absent short sequences which are highly expected to exist) in virus genomes are restriction recognition sites indicating that viruses have probably got rid of these motifs to facilitate invasion of bacterial hosts.[8] Nullomers Database provides a comprehensive collection of minimal absent sequences from hundreds of species and viruses as well as the human and mouse proteomes.

Nullomers have been used as an approach to drug discovery and development. Nullomer peptides were screened for anti-cancer action. Absent sequences have short polyarginine tails added to increase solubility and uptake into the cell, producing peptides called PolyArgNulloPs. One successful sequence, RRRRRNWMWC, was demonstrated to have lethal effects in breast and prostate cancer. It damaged mitochondria by increasing ROS production, which reduced ATP production, leading to cell growth inhibition and cell death. Normal cells show a decreased sensitivity to PolyArgNulloPs over time.[2]

Accidental transfer of biological material containing DNA can produce misleading results. This is a particularly important consideration in forensic and crime labs, where mistakes can cause an innocent person to be convicted of a crime. There was no way to detect if a reference sample was mislabeled as evidence or if a forensic sample is contaminated, but a nullomer barcode can be added to reference samples to distinguish them from evidence on analysis. Tagging can be carried out during sample collection without affecting genotype or quantification results. Impregnated filter paper with various nullomers can be used to soak up and store DNA samples from a crime scene, making the technology simple and effective.[3] Tagging with nullomers can be detected—even when diluted to a million-fold and spilled on evidence, these tags are still clearly detected.[3] Tagging in this way supports National Research Council's recommendations on quality control to reduce fraud and mistakes.[3]