Regulation of human autoimmune regulator (AIRE) gene translation by miR-220b

Tomohito Matsuo, Yukiko Noguchi, Mieko Shindo, Yoshifumi Morita, Yoshie Oda, Eiko Yoshida, Hiroko Hamada, Mine Harada, Yuichi Shiokawa, Takahiro Nishida, Ryuji Tominaga, Yoshikane Kikushige, Koichi Akashi, Jun Kudoh, Nobuyoshi Shimizu, Yuka Tanaka, Tsukuru Umemura, Taketoshi Taniguchi, Akihiko Yoshimura, Takashi KobayashiMasao Mitsuyama, Hironori Kurisaki, Hitoshi Katsuta, Seiho Nagafuchi

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Although mutations of autoimmune regulator (AIRE) gene are responsible for autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), presenting a wide spectrum of many characteristic and non-characteristic clinical features, some patients lack AIRE gene mutations. Therefore, something other than a mutation, such as dysregulation of AIRE gene, may be a causal factor for APECED or its related diseases. However, regulatory mechanisms for AIRE gene expression and/or translation have still remained elusive. We found that IL-2-stimulated CD4+ T (IL-2T) cells showed a high expression of AIRE gene, but very low AIRE protein production, while Epstein-Barr virus-transformed B (EBV-B) cells express both AIRE gene and AIRE protein. By using microarray analysis, we could identify miR-220b as a possible regulatory mechanism for AIRE gene translation in IL-2T cells. Here we report that miR-220b significantly reduced the expression of AIRE protein in AIRE gene with 3'UTR region transfected 293T cells, whereas no alteration of AIRE protein production was observed in the open reading frame of AIRE gene alone transfected cells. In addition, anti-miR-220b reversed the inhibitory function of miR-220b for the expression of AIRE protein in AIRE gene with 3'UTR region transfected cells. Moreover, when AIRE gene transfected cells with mutated 3'UTR were transfected with miR-220b, no reduction of AIRE protein production was observed. Taken together, it was concluded that miR-220b inhibited the AIRE gene translation through the 3'UTR region of AIRE gene, indicating that miR-220b could serve as a regulator for human AIRE gene translation.

Original languageEnglish
Pages (from-to)19-25
Number of pages7
JournalGene
Volume530
Issue number1
DOIs
Publication statusPublished - 2013 Nov 1

Keywords

  • Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
  • Autoimmune regulator gene
  • MicroRNA
  • Translation

ASJC Scopus subject areas

  • Genetics

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  • Cite this

    Matsuo, T., Noguchi, Y., Shindo, M., Morita, Y., Oda, Y., Yoshida, E., Hamada, H., Harada, M., Shiokawa, Y., Nishida, T., Tominaga, R., Kikushige, Y., Akashi, K., Kudoh, J., Shimizu, N., Tanaka, Y., Umemura, T., Taniguchi, T., Yoshimura, A., ... Nagafuchi, S. (2013). Regulation of human autoimmune regulator (AIRE) gene translation by miR-220b. Gene, 530(1), 19-25. https://doi.org/10.1016/j.gene.2013.08.015