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ORF1ab (also ORF1a/b) refers collectively to two open reading frames (ORFs), ORF1a and ORF1b, that are conserved in the genomes of nidoviruses, a group of viruses that includes coronaviruses. The genes express large polyproteins that undergo proteolysis to form several nonstructural proteins with various functions in the viral life cycle, including proteases and the components of the replicase-transcriptase complex (RTC). Together the two ORFs are sometimes referred to as the replicase gene. They are related by a programmed ribosomal frameshift that allows the ribosome to continue translating past the stop codon at the end of ORF1a, in a -1 reading frame. The resulting polyproteins are known as pp1a and pp1ab.

Expression

Genomic information

Genomic organisation of isolate Wuhan-Hu-1, the earliest sequenced sample of SARS-CoV-2, indicating the location of ORF1a and ORF1b
NCBI genome ID	86693
Genome size	29,903 bases
Year of completion	2020
Genome browser (UCSC)

ORF1a is the first open reading frame at the 5' end of the genome. Together ORF1ab occupies about two thirds of the genome, with the remaining third at the 3' end encoding the structural proteins and accessory proteins. It is translated from a 5' capped RNA by cap-dependent translation. Nidoviruses have a complex system of discontinuous subgenomic RNA production to enable expression of genes in their relatively large RNA genomes (typically 27-32kb for coronaviruses), but ORF1ab is translated directly from the genomic RNA. ORF1ab sequences have been observed in noncanonical subgenomic RNAs, though their functional significance is unclear.

A programmed ribosomal frameshift allows reading through the stop codon that terminates ORF1a to continue in a -1 reading frame, producing the longer polyprotein pp1ab. The frameshift occurs at a slippery sequence which is followed by a pseudoknot RNA secondary structure. This has been measured at between 20-50% efficiency for murine coronavirus, or 45-70% in SARS-CoV-2 yielding a stoichiometry of roughly 1.5 to 2 times as much pp1a as pp1ab protein expressed.

Processing

The polyproteins pp1a and pp1ab contain about 13 to 17 nonstructural proteins. They undergo auto-proteolysis to release the nonstructural proteins due to the actions of internal cysteine protease domains.

In coronaviruses, there are a total of 16 nonstructural proteins; pp1a protein contains nonstructural proteins nsp1-11 and the pp1ab protein contains nsp1-10 and nsp12-16. Proteolytic processing is performed by two proteases: the papain-like protease protein domain located in the multidomain protein nsp3 cleaves up to nsp4, and the 3CL protease (also known as the main protease, nsp5) performs the remaining cleavages of nsp5 through the polyprotein C-terminus. Proteins nsp12-16, the C-terminal components of the pp1ab polyprotein, contain the core enzymatic activities necessary for viral replication. After proteolytic processing, several of the nonstructural proteins assemble into a large protein complex known as the replicase-transcriptase complex (RTC) which performs genome replication and transcription.

Components

Core replicase domains

A set of five conserved "core replicase" protein domains are present in all nidovirus lineages (arteriviruses, mesoniviruses, roniviruses, and coronaviruses): from ORF1a, the main protease flanked on either end by transmembrane domains; and from ORF1b, a nucleotidyltransferase domain known as NiRAN, RNA-dependent RNA polymerase (RdRp), a zinc-binding domain, and a helicase. (This is sometimes considered seven domains, counting the transmembrane regions separately.) In addition, an endoribonuclease domain is found in all nidoviruses that infect vertebrate hosts. Arteriviruses, which have smaller genomes than the other nidovirus lineages, also lack methyltransferases as well as a proofreading exoribonuclease, a domain that is conserved in nidoviruses with larger genomes. This proofreading functionality is thought to be required for sufficient fidelity to replicate large RNA genomes, but may also play additional roles in some viruses.

Coronaviruses

In coronaviruses, pp1a and pp1ab together contain sixteen nonstructural proteins, which have the following functions:

Evolution

The structure and organization of the genome, including ORF1a, ORF1b, and the frameshift separating them, is conserved among nidoviruses. Some "non-canonical" nidovirus structures have been described, mainly involving gene fusions. The largest known nidovirus, planarian secretory cell nidovirus (PSCNV), with a 41kb genome, has a non-canonical genome structure in which ORF1a, ORF1b, and downstream ORFs containing structural proteins are fused and expressed as a single large ORF encoding a polyprotein of over 13,000 amino acids. In these non-canonical genomes, other frameshift locations or stop codon readthrough may be used to regulate the stoichiometry of viral proteins.

Nidoviruses vary widely in genome size, from arteriviruses with typically 12-15kb genomes to coronaviruses at 27-32kb. Their evolutionary history has been of research interest in understanding the replication of very large RNA genomes despite the relatively low-fidelity replication mechanism of the viral RNA-dependent RNA polymerase (RdRp). The larger nidovirus genomes (above around 20kb) encode a proofreading exoribonuclease (nsp14 in coronaviruses) thought to be required for replication fidelity.

Among coronaviruses, ORF1ab is more highly conserved than the 3' ORFs encoding structural proteins. Throughout the COVID-19 pandemic, the genome of SARS-CoV-2 viruses has been sequenced many times, resulting in identification of thousands of distinct variants. In a World Health Organization analysis from July 2020, ORF1ab was the most frequently mutated gene, followed by the S gene encoding the spike protein. The most commonly mutated protein within ORF1ab was papain-like protease (nsp3), and the single most commonly observed missense mutation was in RNA-dependent RNA polymerase. Some PCR tests that detect COVID-19 analyze the specimen for the ORF1ab gene, among others.

References

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4. ^ Gulyaeva AA, Gorbalenya AE (January 2021). "A nidovirus perspective on SARS-CoV-2". Biochemical and Biophysical Research Communications. 538: 24–34. doi:10.1016/j.bbrc.2020.11.015. PMC 7664520. PMID 33413979.
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10. Rohaim MA, El Naggar RF, Clayton E, Munir M (January 2021). "Structural and functional insights into non-structural proteins of coronaviruses". Microbial Pathogenesis. 150: 104641. doi:10.1016/j.micpath.2020.104641. PMC 7682334. PMID 33242646.
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14. Richardson, Robin (August 22, 2021). "Open Wide". The Marshall News Messenger. pp. A1, A2. Retrieved 21 November 2022.

v t e Coronavirus genomes
Viral structural protein	spike protein (S) envelope protein (E) membrane protein (M) nucleocapsid protein (N)
Viral nonstructural protein (expressed from ORF1ab)	nonstructural protein 1 nonstructural protein 2 papain-like protease (nsp3) nonstructural protein 4 3C-like protease (nsp5) nonstructural protein 6 nonstructural protein 7 nonstructural protein 8 nonstructural protein 9 nonstructural protein 10 nonstructural protein 11 nonstructural protein 12 nonstructural protein 13 nonstructural protein 14 nonstructural protein 15 nonstructural protein 16
Viral accessory protein	ORF3a ORF3b ORF3c ORF3d ORF6 ORF7a ORF7b ORF8 ORF9b ORF9c ORF10
RNA	Coronavirus 5′ UTR Coronavirus 3′ UTR Coronavirus 3′ UTR pseudoknot Coronavirus 3′ stem-loop II-like motif (s2m) Coronavirus packaging signal Coronavirus frameshifting stimulation element Human identical sequence

• Coronavirus proteins