論文

査読有り 最終著者 責任著者
2018年5月4日

Exogenous TPRX1 homeoprotein modulates the gene expression of lineage-specific transcription factors in human embryonal carcinoma cells

Biotechnology and Biotechnological Equipment
  • Yuki Mori
  • ,
  • Mizuki Sakuraoka
  • ,
  • Takahiro Suzuki
  • ,
  • Sho Sato
  • ,
  • Saiko Sugawara
  • ,
  • Misuzu Hiraide
  • ,
  • Suguru Sato
  • ,
  • Masayuki Kobayashi

32
3
開始ページ
646
終了ページ
652
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1080/13102818.2018.1447396
出版者・発行元
Taylor and Francis Ltd.

We reported previously that EGAM1 homeoproteins (EGAM1 and EGAM1N), transcribed from the Crxos gene as splicing variants, are expressed in preimplantation mouse embryos and mouse embryonic stem (ES) cells. Exogenous expression of these proteins affects the maintenance of an undifferentiated state and the progression of differentiation in mouse ES cells. Human tetrapeptide-repeat homeobox 1 (TPRX1), a member of the eutherian totipotent cell homeobox (ETCHbox) genes, is an ortholog of Crxos. However, the roles of TPRX1 in the differentiation of human pluripotent cells are still unknown. Because the TPRX1 transcripts were undetectable in an undifferentiated state and during the progression of differentiation in wild-type human embryonal carcinoma NT2/D1 cells, it would be advantageous to clarify the relationship between the exogenous expression of TPRX1 and the induction of genes encoding lineage-specific transcription factors in pluripotent cells. The expression of GATA6 and FOXA2, crucial transcription factors for the formation of the primitive endoderm, was upregulated, whereas that of CDX2, a crucial transcription factor for the formation of the trophectoderm, was downregulated by enforced expression of TPRX1. Overall, we suggest that TPRX1 is capable of modulating the expression of lineage-specific transcription factors in pluripotent cells derived from humans.

リンク情報
DOI
https://doi.org/10.1080/13102818.2018.1447396
ID情報
  • DOI : 10.1080/13102818.2018.1447396
  • ISSN : 1310-2818
  • SCOPUS ID : 85043714958

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