Abstract

The H19 gene, one of the best known imprinted genes, encodes a long non-coding RNA that regulates cell proliferation and differentiation. H19 RNA is widely expressed in embryonic tissues, but its expression is restricted in only a few tissues after birth. However, regulation of H19 gene expression remains poorly understood outside the context of genomic imprinting. Here we identified evolutionarily conserved guanine (G)-rich repeated motifs at the 5′ end of the H19 coding region that are consistent with theoretically deduced G-quadruplex sequences. Circular dichroism spectroscopy and electrophoretic mobility shift assays with G-quadruplex-specific ligands revealed that the G-rich motif, located immediately downstream of the transcription start site (TSS), forms a G-quadruplex structure in vitro. By using a series of mutant forms of H19 harboring deletion or G-to-A substitutions, we found that the H19-G-quadruplex regulates H19 gene expression. We further showed that transcription factors Sp1 and E2F1 were associated with the H19-G-quadruplex to either suppress or promote the H19 transcription, respectively. Moreover, H19 expression during differentiation of mouse embryonic stem cells appears to be regulated by a genomic H19 G-quadruplex. These results demonstrate that the G-quadruplex structure immediately downstream of the TSS functions as a novel regulatory element for H19 gene expression.

Highlights

  • The H19 gene encodes a ~2.5 kb transcript that is capped, spliced, and polyadenylated

  • The H19-Igf[2] locus is under the control of genomic imprinting, whereby H19 is expressed from the maternal allele and Igf[2] is expressed from the paternal allele

  • We show that H19 gene transcription is regulated by a G-quadruplex which is located at the region immediately downstream of H19 transcription start sites (TSS)

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Summary

Introduction

The H19 gene encodes a ~2.5 kb transcript that is capped, spliced, and polyadenylated. It has been established that monoallelic expression of H19 genes is regulated by a differentially methylated region (DMR) located between −​2 kb and −​4 kb upstream of the H19 gene locus[26,27,28]. G-quadruplex structures are found in telomeres, promoters and regions proximal to transcription start sites (TSS) of genes[31,32,33,34]. We identify conserved G-rich motifs located immediately downstream of the H19 TSS that forms a G-quadruplex structure. This G-quadruplex structure regulates H19 transcription through binding to transcription factors Sp1 and E2F1. This study demonstrates for the first time the regulation of H19 gene expression via G-quadruplex structure within its coding region

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