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. 2023 Jan 20;11(2):238. doi: 10.3390/vaccines11020238

Table 1.

The efficiency of IRESs in different cell lines.

IRES Cell Line Method of Comparison Results Source
EMCV, CVB3 HEK293, HeLa, A549, Min6 Gaussia luciferase The efficiency of IRESs varies according to cell type; CVB3 IRES was superior in all cell types [9]
EMCV, Poliovirus, KSHV, and HCV HEK293; U87; Huh7; 293T GFP Poliovirus IRES resulted in maximal expression in HEK293 [7]
EMCV and HAV Monkey kidney cells (BT7-H) antibiotic resistance (bacterial chloramphenicol acetyltransferase) EMCV IRES was more efficient than translation directed by the HAV IRES [24]
A synthetic construct with five concatenated copies of the 9-nt Gtx IRES mouse N2a cells Photinus luciferase The efficiency of the translation increases, if several copies of the 9-nt Gtx IRES are included in the construct [25]
EMCV, c-myc, FGF-2, and HTLV-1 B16.F10, TS/A, NIH-3T3, ψCRIP, 293T, and primary cultures of human melanoma cells Immunostaining and flow cytometry The efficiency of translation initiation depends on the type of cells induced and the presence of other genetic elements in the vector. [26]
Five viral (FMDV, HCV, EMCV, PV, HRV)
and eight cellular IRES elements (Rbm3, NRF, Apaf-1, BIP, VCIP, AQP-4, c-myc, CAT-1)
murine fibroblast cell line (NIH 3T3), mouse embryonic fibroblasts (MEF), human hepatoma cell line (Huh 7) and human lung fibroblasts (MRC-5) Firefly and Renilla luciferase Vascular endothelial growth factor and type 1 collagen-inducible protein (VCIP) IRES induced the highest firefly luciferase expression rate in all tested cell lines [27]