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The gap-free human genome was at last officially this year after researchers pieced together the final highly repetitive regions. It includes about 19,400 protein-coding genes in its 3 billion base pairs — but more may be as yet undescribed.

Initial bioinformatics limited protein-coding gene status to open reading frames, or ORFs, 100 amino acids or longer, on the grounds that there are millions of potential ORFs in the transcriptome, and it is likely that many of the shortest appear by chance.

However, ribosome profiling, a technique to sequence messenger RNA captured in the act of being translated, has, over the years, identified thousands of shorter translation products. Many, currently annotated as long noncoding RNAs or untranslated regions of coding mRNAs, have been found in unexpected parts of the genome.

To study the effects of a microprotein, researchers first have to know it exists. A new project aims to develop a catalog of small open reading frames that will be available through bioinformatics archives such as GenBank.

Research on a few of these translated sequences suggests that some of them play important regulatory roles. Nick Ingolia, co-developer of ribosome profiling techniques, said, “We now have several nice examples from a number of (research) groups” of translated products that currently are not annotated as protein-coding genes. “The whole field is trying to sort out order of magnitude; it could be five or 5,000. It’s probably somewhere in between.”

This year, a team of 35 investigators to survey the landscape of small translation products. Examining seven recent ribosome profiling studies, they found 7,264 small translation products ranging from 100 to 16 amino acids long. Roughly half of those appeared in multiple data sets. According to Ariel Bazzini, a Stowers Medical Institute researcher who, like Ingolia, collaborated on this project, there could be many more; the study used conservative numbers and omitted many high-quality ribosome profiling data sets that could have been surveyed for small translation products.

Having assembled this data set, the team now hopes to start probing evolutionary conservation of these small ORFs and whether their associated proteins appear in cells. Validating these small translation products will not be without challenges. The smaller a protein is, the more difficult it is to detect using mass spectrometry and the harder it is to make alterations such as affinity tagging without dramatically altering the end product.

The next step is to understand why these ORFs are translated and whether their products are stable in the cell. Bazzini said that some translation products from so-called untranslated regions of mRNAs act irrespective of their own sequence to regulate the abundance of the main coding protein in the transcript. Small ORFs also perhaps could be translated at random or only in disease contexts such as cancer that disrupt many regulatory pathways. Ascertaining that these proteins really are translated and looking to understand their functions is the consortium’s next planned step.

Meanwhile, the known short proteins can be difficult to find out about, since their identification often is buried in supplementary data sets. Databases including Ensembl, the Human Genome Organization, the Human Proteome Organization, Uniprot and Protein Atlas are working to standardize nomenclature and annotations for these small proteins so knowledge of their existence can reach beyond functional geneticists.