Efficient expression of a heterologous gene in plants depends on the nucleotide composition of mRNA’s 5'-region


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Abstract

The contribution of nucleotide composition of mRNA 5'-region to the efficiency of expression at transcriptional and translational levels was studied in transgenic tobacco plants (Nicotiana tabacum L., cultivar Petit Havana) using a thermostable lichenase reporter gene. Synthetic sequence that contains CG-rich motifs, typical for 5'-region of plant genes, identified in silico, was constructed. Transgenic plant lines of N. tabacum were obtained; they contain thermostable lichenase reporter gene that is under control of the constitutive 35S RNA CaMV promoter and additional regulatory element: synthetic CG-rich sequence, which functions as the 5'-UTR (untranslated region) of the reporter gene mRNA or as 5'-region of the hybrid gene coding sequence, wherein the synthetic sequence is fused with the sequence of the reporter gene in its reading frame. Results of the comparative analysis of mRNA and protein levels in the obtained lines of transgenic plants showed that the synthetic CG-rich sequence significantly increases the level of transcription of the reporter gene and appear to have no negative effect on the efficiency of reporter mRNA translation, which may be due to the peculiarities of its nucleotide composition and structure, namely, due to the presence of motifs that are specific for 5'-regions of plant genes, as well as due to the properties of the secondary structure— the absence of hairpin structures with a high energy of formation. It was experimentally confirmed for the first time that the 5'-region of the genes with a high content of CpG dinucleotides can help to increase the transcription level of genes in plants.

About the authors

A. A. Tyurin

Timiryazev Institute of Plant Physiology; Russian State Agrarian University–Timiryazev Agricultural Academy

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276; ul. Timiryazeva 47, Moscow, 127550

K. V. Kabardaeva

Timiryazev Institute of Plant Physiology; Russian State Agrarian University–Timiryazev Agricultural Academy

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276; ul. Timiryazeva 47, Moscow, 127550

O. A. Gra

Timiryazev Institute of Plant Physiology

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276

O. M. Mustafaev

Timiryazev Institute of Plant Physiology

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276

N. S. Sadovskaya

Timiryazev Institute of Plant Physiology

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276

O. S. Pavlenko

Timiryazev Institute of Plant Physiology; Russian State Agrarian University–Timiryazev Agricultural Academy

Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276; ul. Timiryazeva 47, Moscow, 127550

I. V. Goldenkova-Pavlov

Timiryazev Institute of Plant Physiology; Russian State Agrarian University–Timiryazev Agricultural Academy

Author for correspondence.
Email: irengold58@gmail.com
Russian Federation, ul. Botanicheskaya 35, Moscow, 127276; ul. Timiryazeva 47, Moscow, 127550

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