SARS-CoV-2 Open Reading Frames (ORFs)

SARS-CoV-2 Open Reading Frames (ORFs)

The SARS-CoV-2 genome is ~29 kb divided into 10 open reading frames (ORFs). Each of these ORFs (except seemingly ORF10) is translated in 29 different proteins.

ORF1 is formed by two overlapping ORFs, ORF1a and ORF1b, which are cleaved into 16 nonstructural proteins (NSPs).

ORF2 encodes the Spike (S) glycoprotein.

ORF3a and ORF3b encode themselves.

ORF4 encodes the Envelope (E) protein.

ORF5 encodes the Membrane/Matrix (M) protein.

ORF6 encodes itself.

ORF7a and ORF7b are standalone proteins.

ORF8 encodes itself.

ORF9 is formed by three overlapping ORFs; ORF9a encodes the Nucleocapsid (N) protein and ORF9b and ORF9c encode themselves.

ORF10 seems to encode nothing of importance at this time.

The Different ORF Proteins

The four structural proteins, S, M, N, and E comprise the matura virion. Sixteen non-structural proteins (NSPs_ and nine of the ten ORF proteins have various functions involved in viral replication, modulating the host cell cycle, and evading the host immune response. Summarised briefly here, is what is known and/or postulated to date regarding the various SARS-CoV-2 ORF proteins:

– ORF3a inhibits autophagy by preventing autolysosome formations. Forms homotetrameric potassium-sensitive ion channels. (275 a.a.)

– ORF3b inhibits activation of IFN-I through an unknown mechanism. Generates a strong host immune response. (22 a.a.)

– ORF6 inhibits activation of IFN-I by blocking nuclear translocation of transcription factors. (61 a.a.)

– ORF7a suppresses antigen-presentation in monocytes and after ubiquitination, suppresses STAT2 phosphorylation thereby inhibiting activation of IFN-I. (121 a.a.)

– ORF7b inhibits activation of IFN-I by inhibiting phosphorylation of STAT1 and STAT2. May have leucine zipper functionality. (43 a.a.)

– ORF8 downregulates MHC-I in vitro, inhibiting antigen presentation. Also generates a strong host immune response. (121 a.a.)

– ORF9b inhibits activation of IFN-I by targeting IKK? (NEMO) and TOM70. (97 a.a.)

– ORF9c may interfere with IFN signalling, but it is still being investigated. (73 a.a.)

– ORF10 is not essential for viral replication and variants without this are fully functional. (~38 a.a.)

ProSci’s COVID-19 Research

ProSci is committed to furthering global research efforts to understand this novel virus and the disease it causes by offering a broad catalogue of SARS-CoV-2 antibodiesrecombinant proteins, and related research reagents. Current research shows that inhibiting some of the accessory proteins can aid in overcoming immune evasion and suppression thereby allowing the host to fight off the infection. Let ProSci’s antibodies and proteins help further your research into these potential treatment options.

References

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Miao, G., Zhao, H., Li, Y., Ji, M., Chen, Y., Shi, Y., Bi, Y., Wang, P., & Zhang, H. (2021). ORF3a of the COVID-19 virus SARS-CoV-2 blocks HOPS complex-mediated assembly of the SNARE complex required for autolysosome formation. Developmental Cell, 56(4), 427-442.e5. https://doi.org/10.1016/j.devcel.2020.12.010

Majumdar, P., & Niyogi, S. (2020). ORF3a mutation associated with higher mortality rate in SARS-CoV-2 infection. Epidemiology and Infection, 148. https://doi.org/10.1017/s0950268820002599

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Zhou, Z., Huang, C., Zhou, Z., Huang, Z., Su, L., Kang, S., Chen, X., Chen, Q., He, S., Rong, X., Xiao, F., Chen, J., & Chen, S. (2021). Structural insight reveals SARS-CoV-2 ORF7a as an immunomodulating factor for human CD14+ monocytes. IScience, 24(3), 102187. https://doi.org/10.1016/j.isci.2021.102187

Cao, Z., Xia, H., Rajsbaum, R., Xia, X., Wang, H., & Shi, P.-Y. (2021). Ubiquitination of SARS-CoV-2 ORF7a promotes antagonism of interferon response. Cellular & Molecular Immunology, 18(3), 746–748. https://doi.org/10.1038/s41423-020-00603-6

Nizamudeen, Z. A., Xu, E.-R., Karthik, V., Halawa, M., Arkill, K. P., Jackson, A. M., Bates, D. O., & Emsley, J. (2021). Structural assessment of SARS-CoV2 accessory protein ORF7a predicts LFA-1 and Mac-1 binding potential. Bioscience Reports, 41(1). https://doi.org/10.1042/bsr20203837

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Zinzula, L. (2021). Lost in deletion: The enigmatic ORF8 protein of SARS-CoV-2. Biochemical and Biophysical Research Communications, 538, 116–124. https://doi.org/10.1016/j.bbrc.2020.10.045

Wu, J., Shi, Y., Pan, X., Wu, S., Hou, R., Zhang, Y., Zhong, T., Tang, H., Du, W., Wang, L., Wo, J., Mu, J., Qiu, Y., Yang, K., Zhang, L.-K., Ye, B.-C., & Qi, N. (2021). SARS-CoV-2 ORF9b inhibits RIG-I-MAVS antiviral signaling by interrupting K63-linked ubiquitination of NEMO. Cell Reports, 34(7), 108761. https://doi.org/10.1016/j.celrep.2021.108761

Jiang, H., Zhang, H., Meng, Q., Xie, J., Li, Y., Chen, H., Zheng, Y., Wang, X., Qi, H., Zhang, J., Wang, P.-H., Han, Z.-G., & Tao, S. (2020). SARS-CoV-2 Orf9b suppresses type I interferon responses by targeting TOM70. Cellular & Molecular Immunology, 17(9), 998–1000. https://doi.org/10.1038/s41423-020-0514-8

Dominguez Andres, A., Feng, Y., Campos, A. R., Yin, J., Yang, C.-C., James, B., Murad, R., Kim, H., Deshpande, A. J., Gordon, D. E., Krogan, N., Pippa, R., & Ronai, Z. A. (2020). SARS-CoV-2 ORF9c Is a Membrane-Associated Protein that Suppresses Antiviral Responses in Cells. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.08.18.256776

Pancer, K., Milewska, A., Owczarek, K., Dabrowska, A., Kowalski, M., ?abaj, P. P., Branicki, W., Sanak, M., & Pyrc, K. (2020). The SARS-CoV-2 ORF10 is not essential in vitro or in vivo in humans. PLOS Pathogens, 16(12), e1008959. https://doi.org/10.1371/journal.ppat.1008959

Originally posted by ProSci on https://www.prosci-inc.com/blog/sars-cov-2-orfs/

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SARS-CoV-2 Open Reading Frames (ORFs)
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