抄録
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.
| 本文言語 | English |
|---|---|
| ページ(範囲) | 10742-10752 |
| ページ数 | 11 |
| ジャーナル | Nucleic acids research |
| 巻 | 40 |
| 号 | 21 |
| DOI | |
| 出版ステータス | Published - 2012 11月 |
| 外部発表 | はい |
ASJC Scopus subject areas
- 遺伝学
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