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Mol Cell Biol. 2015 Oct;35(19):3436-45. doi: 10.1128/MCB.00381-15. Epub 2015 Jul 13.

Expression of the CTCFL Gene during Mouse Embryogenesis Causes Growth Retardation, Postnatal Lethality, and Dysregulation of the Transforming Growth Factor β Pathway.

Author information

1
Department of Histology and Embryology, Akdeniz University School of Medicine, Antalya, Turkey.
2
Department of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
3
Department of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut, USA james.mcgrath@yale.edu.

Abstract

CTCFL, a paralog of CTCF, also known as BORIS (brother of regulator of imprinted sites), is a testis-expressed gene whose function is largely unknown. Its product is a cancer testis antigen (CTA), and it is often expressed in tumor cells and also seen in two benign human vascular malformations, juvenile angiofibromas and infantile hemangiomas. To understand the function of Ctcfl, we created tetracycline-inducible Ctcfl transgenic mice. We show that Ctcfl expression during embryogenesis results in growth retardation, eye malformations, multiorgan pathologies, vascular defects, and neonatal death. This phenotype resembles prior mouse models that perturb the transforming growth factor β (TGFB) pathway. Embryonic stem (ES) cells with the Ctcfl transgene reproduce the phenotype in ES cell-tetraploid chimeras. Transcriptome sequencing of the Ctcfl ES cells revealed 14 genes deregulated by Ctcfl expression. Bioinformatic analysis revealed the TGFB pathway as most affected by embryonic Ctcfl expression. Understanding the consequence of Ctcfl expression in nontesticular cells and elucidating downstream targets of Ctcfl could explain the role of its product as a CTA and its involvement in two, if not more, human vascular malformations.

PMID:
26169830
PMCID:
PMC4561735
DOI:
10.1128/MCB.00381-15
[Indexed for MEDLINE]
Free PMC Article
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