An internal ribosome entry site, abbreviated IRES, is an RNA element that allows for translation initiation in a cap-independent manner, as part of the greater process of protein synthesis. Initiation of eukaryotic translation nearly always occurs at and is dependent on the 5' cap of mRNA molecules, where the translation initiation complex forms and ribosomes engage the mRNA. IRES elements, however allow ribosomes to engage the mRNA and begin translation independently of the 5' cap.

History

IRES sequences were first discovered in 1988 in the poliovirus (PV) and encephalomyocarditis virus (EMCV) RNA genomes in the laboratories of Nahum Sonenberg[1] and Eckard Wimmer,[2] respectively. They are described as distinct regions of RNA molecules that are able to recruit the eukaryotic ribosome to the mRNA. This process is also known as cap-independent translation. It has been shown that IRES elements have a distinct secondary or even tertiary structure, but similar structural features at the levels of either primary or secondary structure that are common to all IRES segments have not been reported to date.

Use of IRES sequences in molecular biology soon became common as a tool for expressing multiple genes from a single transcriptional unit in a genetic vector. In such vectors, translation of the first cistron is initiated at the 5' cap, and translation of any downstream cistron is enabled by an IRES element appended at its 5' end.[3]

Location

Poliovirus genome, including an IRES.

IRES elements are most commonly found in the 5' untranslated region, but may also occur elsewhere in mRNAs. The mRNA of viruses of the Dicistroviridae family possess two open reading frames (ORFs), and translation of each is directed by a distinct IRES. It has also been suggested that some mammalian cellular mRNAs also have IRESs, although this has been a matter of dispute.[4][5] A number of these cellular IRES elements are located within mRNAs encoding proteins involved in stress survival, and other processes critical to survival. As of September 2009, there are 60 animal and 8 plant viruses reported to contain IRES elements and 115 mRNA sequences containing them as well.[6]

Activation

IRESs are often used by viruses as a means to ensure that viral translation is active when host translation is inhibited. These mechanisms of host translation inhibition are varied, and can be initiated by both virus and host, depending on the type of virus. However, in the case of most picornaviruses, such as poliovirus, this is accomplished by viral proteolytic cleavage of eIF4G so that it cannot interact with the 5'cap binding protein eIF4E. Interaction between these two eukaryotic initiation factors (eIFs) of the eIF4F complex is necessary for 40S ribosomal subunit recruitment to the 5' end of mRNAs, which is further thought to occur with mRNA 5'cap to 3' poly(A) tail loop formation. The virus may even use partially-cleaved eIF4G to aid in initiation of IRES-mediated translation.

Cells may also use IRESs to increase translation of certain proteins during mitosis and programmed cell death. In mitosis, the cell dephosphorylates eIF4E so that it has little affinity for the 5'cap. As a result, the 40S ribosomal subunit, and the translational machinery is diverted to IRES within the mRNA. Many proteins involved in mitosis are encoded by IRES mRNA. In programmed cell death, cleavage of eIF-4G, such as performed by viruses, decreases translation. Lack of essential proteins contributes to the death of the cell, as does translation of IRES mRNA sequences coding proteins involved in controlling cell death.[7]

Mechanism

To date, the mechanism of viral IRES function is better characterized than the mechanism of cellular IRES function,[8] which is still a matter of debate. HCV-like IRESs directly bind the 40S ribosomal subunit to position their initiator codons are located in ribosomal P-site without mRNA scanning. These IRESs still use the eukaryotic initiation factors (eIFs) eIF2, eIF3, eIF5, and eIF5B, but do not require the factors eIF1, eIF1A, and the eIF4F complex. In contrast, picornavirus IRESs do not bind the 40S subunit directly, but are recruited instead through the eIF4G-binding site.[9] Many viral IRES (and cellular IRES) require additional proteins to mediate their function, known as IRES trans-acting factors (ITAFs). The role of ITAFs in IRES function is still under investigation.

Validity of Tests for IRES function

Testing of sequences for potential IRES function has generally relied on the use of bicistronic reporter assays. In these tests, a candidate IRES segment is introduced into a plasmid between two cistrons encoding two different reporter proteins. A promoter upstream of the first cistron drives transcription of both cistrons in a single mRNA. Cells are transfected with the plasmid and assays are subsequently performed to quantitate expression of the two reporters in the cells. An increase in the ratio of expression of the downstream reporter relative to the upstream reporter is taken as evidence for IRES activity in the test sequence. However, without characterization of the mRNA species produced from such plasmids, other explanations for the increase in this ratio cannot be ruled out.[10][11] For example, there are multiple known cases of suspected IRES elements that were later reported as having promoter function. Unexpected splicing activity within several reported IRES elements have also been shown to be responsible for the apparent IRES function observed in bicistronic reporter tests.[12] A promoter or splice acceptor within a test sequence can result in the production of monocistronic mRNA from which the downstream cistron is translated by conventional cap-dependent, rather than IRES-mediated, initiation. A later study that documented a variety of unexpected aberrant mRNA species arising from reporter plasmids revealed that splice acceptor sites can mimic both IRES and promoter elements in tests employing such plasmids, further highlighting the need for caution in the interpretation of reporter assay results in the absence of careful RNA analysis.[13]

Applications

IRES sequences are often used in molecular biology to co-express multiple genes under the control of the same promoter, thereby mimicking a polycistronic mRNA. Within the past decades, IRES sequences have been used to develop hundreds of genetically modified rodent animal models. [14] The advantage of this technique is that molecular handling is improved. The problem about IRES is that the expression for each subsequent gene is decreased.[15]

Another viral element to establish polycistronic mRNA in eukaryotes are 2A-peptides. Here, the potential decrease in gene expression and the degree of incomplete separation of proteins is context dependent.[16]

Types

Internal ribosome entry sites in viral genomes[9]
VirusIRES
PoliovirusPicornavirus IRES
RhinovirusPicornavirus IRES
Encephalomyocarditis virusPicornavirus IRES
Foot-and-mouth disease virusAphthovirus IRES
Kaposi's sarcoma-associated herpesvirus (KSHV)Kaposi's sarcoma-associated herpesvirus IRES
Hepatitis A virusHepatitis A IRES
Hepatitis C virusHepatitis C IRES
Classical swine fever virusPestivirus IRES
Bovine viral diarrhea virusPestivirus IRES
Friend murine leukemia
Moloney murine leukemia (MMLV)
Rous sarcoma virus
Human immunodeficiency virus
Plautia stali intestine virusCripavirus internal ribosome entry site (IRES)
Cricket paralysis virusCripavirus internal ribosome entry site (IRES)
Triatoma virusCripavirus internal ribosome entry site (IRES)
Rhopalosiphum padi virusRhopalosiphum padi virus internal ribosome entry site (IRES)
Marek's disease virus MDV5'Leader IRES and intercistronic IRES in the 1.8-kb family of immediate early transcripts (IRES)1
Internal ribosome entry sites in cellular mRNAs[9]
Protein typeProteins
Growth factorsFibroblast growth factor (FGF-1 IRES and FGF-2 IRES), Platelet-derived growth factor B (PDGF/c-sis IRES), Vascular endothelial growth factor (VEGF IRES), Insulin-like growth factor 2 (IGF-II IRES)
Transcription factorsAntennapedia, Ultrabithorax, MYT-2, NF-κB repressing factor NRF, AML1/RUNX1, Gtx homeodomain protein
Translation factorsEukaryotic initiation factor 4G (elF4G)a, Eukaryotic initiation factor 4Gl (elF4Gl)a, Eukaryotic translation initiation factor 4 gamma 2 (EIF4G2,DAP5)
Oncogenesc-myc, L-myc, Pim-1, Protein kinase p58PITSLRE, p53
Transporters/receptorsCationic amino acid transporter (SLC7A1,Cat-1), Nuclear form of Notch 2, Voltage-gated potassium channel
Activators of apoptosisApoptotic protease activating factor (Apaf-1)
Inhibitors of apoptosisX-linked inhibitor of apoptosis (XIAP), HIAP2, Bcl-xL, Bcl-2
Proteins localized in neuronal dendritesActivity-regulated cytoskeletal protein (ARC), α-subunit of calcium calmodulin dependent kinase II dendrin, Microtubule-associated protein 2 (MAP2), neurogranin (RC3), Amyloid precursor protein
OthersImmunoglobulin heavy chain binding protein (BiP), Heat shock protein 70, β-subunit of mitochondrial H+-ATP synthase, Ornithine decarboxylase, connexins 32 and 43, HIF-1α, APC

See also

References

  1. ↑ Pelletier J, Sonenberg N (July 1988). "Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA". Nature. 334 (6180): 320–325. Bibcode:1988Natur.334..320P. doi:10.1038/334320a0. PMID 2839775. S2CID 4327857.
  2. ↑ Jang SK, Kräusslich HG, Nicklin MJ, Duke GM, Palmenberg AC, Wimmer E (August 1988). "A segment of the 5' nontranslated region of encephalomyocarditis virus RNA directs internal entry of ribosomes during in vitro translation". Journal of Virology. 62 (8): 2636–2643. doi:10.1128/jvi.62.8.2636-2643.1988. PMC 253694. PMID 2839690.
  3. ↑ Renaud-Gabardos, E; Hantelys, F; Morfoisse, F; Chaufour, X; Garmy-Susini, B; Prats, AC (20 February 2015). "Internal ribosome entry site-based vectors for combined gene therapy". World Journal of Experimental Medicine. 5 (1): 11–20. doi:10.5493/wjem.v5.i1.11. PMC 4308528. PMID 25699230.
  4. ↑ Kozak M (March 2001). "New ways of initiating translation in eukaryotes?". Mol Cell Biol. 21 (6): 1899–1907. doi:10.1128/MCB.21.6.1899-1907.2001. PMC 86772. PMID 11238926.
  5. ↑ Kozak M (2005). "A second look at cellular mRNA sequences said to function as internal ribosome entry sites". Nucleic Acids Research. 33 (20): 6593–6602. doi:10.1093/nar/gki958. PMC 1298923. PMID 16314320.
  6. ↑ Mokrejs M, Vopálenský V, Kolenaty O, Masek T, Feketová Z, Sekyrová P, Skaloudová B, Kríz V, Pospísek M (January 2006). "IRESite: the database of experimentally verified IRES structures (www.iresite.org)". Nucleic Acids Research. 34 (Database issue): D125–30. doi:10.1093/nar/gkj081. PMC 1347444. PMID 16381829.
  7. ↑ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). Molecular Biology of the Cell. Garland Science. pp. 447–448. ISBN 978-0-8153-4072-0.
  8. ↑ López-Lastra M, Rivas A, Barría MI (2005). "Protein synthesis in eukaryotes: the growing biological relevance of cap-independent translation initiation". Biological Research. 38 (2–3): 121–146. CiteSeerX 10.1.1.463.2059. doi:10.4067/s0716-97602005000200003. PMID 16238092.
  9. 1 2 3 Hellen CU, Sarnow P (July 2001). "Internal ribosome entry sites in eukaryotic mRNA molecules". Genes & Development. 15 (13): 1593–1612. doi:10.1101/gad.891101. PMID 11445534.
  10. ↑ Kozak M (March 2001). "New ways of initiating translation in eukaryotes?". Mol Cell Biol. 21 (6): 1899–1907. doi:10.1128/MCB.21.6.1899-1907.2001. PMC 86772. PMID 11238926.
  11. ↑ Kozak M (2005). "A second look at cellular mRNA sequences said to function as internal ribosome entry sites". Nucleic Acids Research. 33 (20): 6593–6602. doi:10.1093/nar/gki958. PMC 1298923. PMID 16314320.
  12. ↑ Baranick BT, Lemp NA, Nagashima J, Hiraoka K, Kasahara N, Logg CR (March 2008). "Splicing mediates the activity of four putative cellular internal ribosome entry sites". Proceedings of the National Academy of Sciences of the United States of America. 105 (12): 4733–4738. Bibcode:2008PNAS..105.4733B. doi:10.1073/pnas.0710650105. PMC 2290820. PMID 18326627.
  13. ↑ Lemp NA, Hiraoka K, Kasahara N, Logg CR (August 2012). "Cryptic transcripts from a ubiquitous plasmid origin of replication confound tests for cis-regulatory function". Nucleic Acids Res. 40 (15): 7280–7290. doi:10.1093/nar/gks451. PMC 3424574. PMID 22618870.
  14. ↑ Shaimardanova, AA; Chulpanova, DS (2019). "Production and Application of Multicistronic Constructs for Various Human Disease Therapies". Pharmaceutics. 11 (11): 580–590. doi:10.3390/pharmaceutics11110580. PMC 6920891. PMID 31698727.
  15. ↑ Michnick, Donna; Wasley, Louise C.; Davies, Monique V.; Kaufman, Randal J. (1991-08-25). "Improved vectors for stable expression of foreign genes in mammalian cells by use of the untranslated leader sequence from EMC virus". Nucleic Acids Research. 19 (16): 4485–4490. doi:10.1093/nar/19.16.4485. ISSN 0305-1048. PMC 328638. PMID 1653417.
  16. ↑ Xia, Qingyou; Ping Zhao; Wang, Riyuan; Wang, Feng; Wang, Yuancheng (2015-11-05). "2A self-cleaving peptide-based multi-gene expression system in the silkworm Bombyx mori". Scientific Reports. 5: 16273. Bibcode:2015NatSR...516273W. doi:10.1038/srep16273. PMC 4633692. PMID 26537835.
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