30.11.2020 08:05 Age: 52 days

On the trail of the genetic code - Overlapping gene found in SARS-CoV-2

Category: Research

Viruses are infectious organic structures that spread by transmission and can only multiply within a suitable host cell. To understand how new viruses are created, it is necessary to determine the position of the individual genes precisely and comprehensively and to clarify what these genes do. However, viruses often have so-called “overlapping genes,” which can easily be overlooked but may play an important role in virus spread, even up to the level of a pandemic.

Deciphering the gene structure of the corona virus is an exciting task.

Deciphering the gene structure of the corona virus is an exciting task. (Picture Pixabay/ Pete Linforth)

A research team in the department of Microbial Ecology at the  Technical University of Munich (TUM)  School of life Sciences on the Weihenstephan Campus has now found a previously hidden gene that may have contributed to the unique biology of SARS-CoV-2 and thus to its rapid spread.  TUM scientist Zachary Ardern has studied the matter in great detail.  In this interview, he talks about his research results.

You do research on overlapping genes.  How should one think of your field of research?

At first glance, genes appear to be like written language because they consist of letter strings (nucleotides) that convey information.  However, while the individual units of language, that is to say written words, can only be arranged one after the other, genes can be overlapping and multifunctional, with information being cryptically encoded, depending on which letter you start with.  Overlapping genes or “genes within genes” are difficult to identify.  They are particularly common in viruses that have been refined by natural selection to maximise their replication and thus the information content per nucleotide.

Which question have you now investigated specifically with regard to the corona virus?

If overlapping genes with functional significance are overlooked, important aspects of viral biology can be misunderstood.  Even before the COVID 19 pandemic, we had developed a method of studying overlapping genes, “OLGenie“.  This method  searches genomes for patterns of genetic alterations that are unique to overlapping genes.  We have now applied this as well as other methods to the wealth of new sequence data available for SARS-CoV-2.

What have been your most important results?

We have identified ORF3d, a new overlapping gene in SARS-CoV-2 that has the potential to encode an unexpectedly long protein.  We have found that this gene is also present in a previously discovered pangolin coronavirus, which is a relative of SARS-CoV-2.  However, the new ORF3d was previously misclassified.  As a result, its function was not predicted accurately. We have now described the evolution of this gene in detail, have shown that it is likely functional, and have distinguished it from the various other overlapping genes currently recognized in SARS-CoV-2.  

Who could ultimately benefit from the results of your study, and what would need to be done before we could achieve these benefits?

In terms of genome size, SARS-CoV-2 and its many relatives are among the longest RNA viruses in existence and have a very low mutation rate.  They may therefore be more susceptible to “genomic tricks” than other RNA viruses.  Overlapping genes may be one of the many ways corona viruses have evolved to efficiently replicate, thwart host immunity, and transmit themselves.  Knowing that there are overlapping genes and how they work may reveal new ways of controlling coronaviruses with vaccines and antiviral drugs.

Further information:

The team involved was international and was led by three postdoctoral researchers in Taiwan,  TUM-Weihenstephan and California.  It included researchers from both the department of Microbial Ecology and BayBioMS (Bavarian Center for Biomolecular Mass Spectrometry).  The methods used are directly based on years of basic scientific research on overlapping genes at the department of Microbial Ecology chaired by Professor Siegfried Scherer.The chair is associated with the ZIEL - Institute for Food and Health.

Link to the publication: https://elifesciences.org/articles/59633

Susanne Neumann/ Dr. Katharina Baumeister-Krojer
TUM School of Life Sciences
Corporate Communications Center
Mail: susanne.neumann[at]tum.de

Scientific Contact:
Dr. Zachary Ardern
Chair for Microbial Ecology
Scientific assistant
Mail: zachary.ardern[at]tum.de
Phone: +49 8161.71.3851