Cdx2 represses Oct4 function via inducing its proteasome-dependent degradation in early porcine embryos

Developmental Biology

Volumn 410, Issue 1, 2016, Pages 36-44

  Bou, Gerelchimeg ^a   Liu, Shichao ^a   Guo, Jia ^a   Zhao, Yueming ^a   Sun, Mingju ^a   Xue, Binghua ^a   Wang, Jiaqiang ^a   Wei, Yanchang ^a   Kong, Qingran ^a   Liu, Zhonghua ^a  

^a NORTHEAST AGRICULTURAL UNIVERSITY   (China)

Author keywords

Cdx2; Early embryo; Molecular interaction; Oct4; Pig; Proteasomal degradation

Indexed keywords

OCTAMER TRANSCRIPTION FACTOR 4; PROTEASOME; TRANSCRIPTION FACTOR CDX2; BENZYLOXYCARBONYLLEUCYL-LEUCYL-LEUCINE ALDEHYDE; HOMEODOMAIN PROTEIN; LEUPEPTIN; MESSENGER RNA; OCTAMER TRANSCRIPTION FACTOR;

ANIMAL CELL; ARTICLE; BINDING SITE; CELL CYCLE ARREST; CELL LINEAGE; COMPLEX FORMATION; CONTROLLED STUDY; EMBRYO; GENE OVEREXPRESSION; GENE SEGREGATION; INNER CELL MASS; NONHUMAN; PIG; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROCESSING; PROTEIN PROTEIN INTERACTION; TRANSCRIPTION REGULATION; TROPHECTODERM; TROPHOBLAST; ACTIVE TRANSPORT; ANIMAL; CELL CULTURE; EMBRYOLOGY; GENETICS; PHYSIOLOGY;

ACTIVE TRANSPORT, CELL NUCLEUS; ANIMALS; CELLS, CULTURED; HOMEODOMAIN PROTEINS; LEUPEPTINS; OCTAMER TRANSCRIPTION FACTORS; PROTEASOME ENDOPEPTIDASE COMPLEX; RNA, MESSENGER; SWINE;

EID: 84961207073     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2015.12.014     Document Type: Article

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