Class Ia molecules of human leucocyte antigen (HLA-A,-B and-C) are widely expressed and play a central role in the immune system by presenting peptides derived from the lumen of the endoplasmic reticulum. In contrast, class Ib molecules such as HLA-G serve novel functions. The distribution of HLA-G is mostly limited to foetal trophoblastic tissues and some tumour tissues. The mechanism required for the tissue-specific regulation of the HLA-G gene has not been well understood. Here, we investigated the genomic regulation of HLA-G by manipulating one copy of a genomic DNA fragment on a human artificial chromosome. We identified a potential negative regulator of gene expression in a sequence upstream of HLA-G that overlapped with the long interspersed element (LINE1); silencing of HLA-G involved a DNA secondary structure generated in LINE1. The presence of a LINE1 gene silencer may explain the limited expression of HLA-G compared with other class I genes. © 2012 The Author(s).
Ikeno, M., Suzuki, N., Kamiya, M., Takahashi, Y., Kudoh, J., & Okazaki, T. (2012). LINE1 family member is negative regulator of HLA-G expression. Nucleic Acids Research, 40(21), 10742–10752. https://doi.org/10.1093/nar/gks874