Copper chaperone ATOX1 regulates pluripotency factor OCT4 in preimplantation mouse embryos

被引:10
|
作者
Celauro, Emanuele [1 ]
Mukaj, Amisa [1 ]
Fierro-Gonzalez, Juan Carlos [1 ]
Wittung-Stafshede, Pernilla [1 ]
机构
[1] Chalmers, Dept Biol & Biol Engn, S-41296 Gothenburg, Sweden
关键词
Atox1; Preimplantation mouse embryo; Development; Transcription factor; Oct4; TRANSPORT PROTEIN ANTIOXIDANT-1; STEM-CELLS; MAMMALIAN EMBRYO; GENE-EXPRESSION; TRANSCRIPTION; TROPHECTODERM; LINEAGE; DIFFERENTIATION; SPECIFICATION; BLASTOCYST;
D O I
10.1016/j.bbrc.2017.07.064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite of the importance of copper (Cu) during pregnancy, the roles of Cu-binding proteins during early embryonic development are unknown. The Cu chaperone ATOX1 was recently suggested to have additional functions related to transcription and cancer. When we analyzed single-cell RNA transcript data from early mouse embryos, Atox1 transcript levels increased dramatically at the 8-cell stage and, at 16 and 32-cell embryo stages, matched those of Oct4 which expresses a transcription factor essential for pluripotency in the inner cell mass. To explore this, we probed Atox1 expression during the first week of development of mouse embryos. ATOX1 appeared ubiquitously expressed throughout the cells until compaction; in subsequent embryo stages, ATOX1 relocalized to cytoplasmic perinuclear domains in the inner cell mass. Silencing of Oct4 did not affect Atoxl expression, but silencing of Atoxl at the 2-cell stage strongly diminished Oct4 expression in 16-cell embryos. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:147 / 153
页数:7
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