Construction of a general piggyBac transposon inducible cell immortalization vector and verification of its basic properties.
- Author:
Hui HUANG
;
Guangdong HU
;
Jian KANG
;
Suzhu QING
;
Yong ZHANG
- Publication Type:Journal Article
- MeSH:
Cell Line;
DNA Transposable Elements;
genetics;
Genetic Vectors;
Green Fluorescent Proteins;
genetics;
HEK293 Cells;
Humans;
Plasmids;
Polymerase Chain Reaction;
Telomerase;
genetics;
Transfection
- From:
Chinese Journal of Biotechnology
2014;30(8):1182-1192
- CountryChina
- Language:Chinese
-
Abstract:
In order to construct generally efficient cell immortalization vector, pTP-hTERT, we modified the traditional piggyBac (PB) transposon using artificial synthesis, PCR and enzyme digestion. The modified vector contained the necessary transposon elements, a PB transposase expression cassette, a co-expression selectable element and a human telomerase reverse transcriptase (hTERT) expression cassette. The co-expression selectable element had two markers, enhanced green fluorescent protein (EGFP) gene and puromycin-resistance (Puro) gene, linked by porcine teschovirus-1 2A peptide (P2A). To validate the functionality of vector elements, we transfected pTP-hTERT into HEK293 cell, selected the positive cell clones and then conducted RT-PCR, Western blotting (WB) and Tail-PCR, methylene blue staining and statistic analysis on selected cells. The results of sequencing and cell culture show that the pTP-hTERT was constructed successfully and the positive cell could be selected by puromycin. The WB results, P2A cutting EGFP and Puro fusion protein with high efficiency, reflected the selectable element worked. The sequencing result of Tail-PCR confirmed the vector integrated into the genome through transposition. The results of methylene blue staining and statistic analysis indicated the clone of positive cells triggered by pTP-hTERT significantly increased (P < 0.01) compared with control group. The construction of pTP-hTERT provides an efficient tool for establishing immortalized cell lines and a demonstration for building other eukaryotic plasmids.
