The regulatory function of tandem repeat VNTR2‐1 in hTERT gene involves basic Helix–loop–helix family transcription factors

Abstract

Telomerase is a ribonucleoprotein enzyme that synthesizes telomere end sequence. The expression of hTERT gene, encoding the catalytic subunit of human telomerase, is restricted to highly proliferative tissues and is undetectable in most somatic cells. Abnormal activation of hTERT gene is found in 90% of human tumors. Previously, we identified tandem repeat of 42‐bp/unit, VNTR2‐1, in intron 2 of the hTERT gene, as a novel regulatory element important for hTERT transcription in cancer cells. In the current study, we found that multiple 42‐bp repeats of VNTR2‐1 activated luciferase gene in reporter plasmids. Mutation of the predicted cis‐regulatory elements within the 42‐bp repeats, including a E‐box motif, resulted in a partial or complete loss of its enhancer activity. Moreover, MYC family proteins, c‐MYC, MAX, and MNT, regulated hTERT gene transcription through both VNTR2‐1 and E‐boxes at the proximal hTERT promoter. Chromatin segmentation analysis of published ChIP‐sequencing data from K562 cells indicated that VNTR2‐1 was a bivalent enhancer. In telomerase‐expressing human melanoma cell line MelJuSo, deletion of VNTR2‐1 caused the hTERT promoter chromatin status to change from an active state to a repressed state, accompanied by increases of H3K27me3 and H3K9me3 marks. Therefore, we provided additional evidence for VNTR2‐1 as a functional regulatory element that regulated hTERT expression by MYC family transcription factors. These results have improved our knowledge on the functions of repetitive genomic DNAs and the regulatory mechanisms of human telomerase gene.

An easy method to improve the recombinant efficiency of psi-CHECK2

“…Up to date, the traditional method (as described for Group-3) is still widely used to construct various recombinant vectors such as psi-CHECK2 because of the low cost and easy access of the materials [6,14,15]. To improve the recombinant efficiency of the traditional method, innovation has been developed.…”