The multigene expression system is highly attractive to co-express multiple genes or multi-subunit complex-based genes for their functional studies， and in gene therapy and visual tracking of expressed proteins. However， the current multiple gene co-expression strategies usually suffer from severe inefficiency and unbalanced expression of multiple genes. Here， we report on an improved 2A self-cleaving peptide (2A)-based multigene expression system (2A-MGES)， by introducing an optimized Kozak region (Ck) and altering the gene arrangement， both of which contributed to the efficient expression of two fluorescent protein genes in silkworm. By co-expressing DsRed and EGFP genes in insect cells and silkworm... More
The multigene expression system is highly attractive to co-express multiple genes or multi-subunit complex-based genes for their functional studies， and in gene therapy and visual tracking of expressed proteins. However， the current multiple gene co-expression strategies usually suffer from severe inefficiency and unbalanced expression of multiple genes. Here， we report on an improved 2A self-cleaving peptide (2A)-based multigene expression system (2A-MGES)， by introducing an optimized Kozak region (Ck) and altering the gene arrangement， both of which contributed to the efficient expression of two fluorescent protein genes in silkworm. By co-expressing DsRed and EGFP genes in insect cells and silkworms， the potent Ck was first found to improve the translation efficiency of downstream genes， and the expression of the flanking genes of 2A were improved by altering the gene arrangement in 2A-MGES. Moreover， we showed that combining Ck and an optimized gene arrangement in 2A-MGES could synergistically improve the expression of genes in the cell. Further， these two flanking genes， regulated by modified 2A-MGES， were further co-expressed in the middle silk gland and secreted into the cocoon， and both achieved efficient expression in the transgenic silkworms and their cocoons. These results suggested that the modified Ck-2A-MGES will be a potent tool for multiple gene expression， for studies of their functions， and their applications in insect species.
