| Literature DB >> 28347816 |
Sébastien Szuplewski1, Nesrine Maharzi2, Elisabeth Nelson2, Kutaiba Alhaj Hussen2, Bernard Mignotte1, Isabelle Guénal3, Bruno Canque2.
Abstract
Human KIAA0922/TMEM131L encodes a transmembrane protein, TMEM131L, that regulates the canonical Wnt/β-catenin signaling pathway by eliciting the lysosome-dependent degradation of phosphorylated LRP6 co-receptor. Here, we use a heterospecific Drosophila transgenic model to examine the potential evolutionary conservation of TMEM131L function. Analysis of TMEM131L transgenic flies shows that TMEM131L interference with the Wnt pathway results primarily from a Notch-dependent decrease in Wingless production. Consistently, lentivirus-mediated overexpression of TMEM131L in human CD34+ hematopoietic progenitor cells leads to decreased susceptibility to Notch1 ligation and defective commitment toward the T lineage. These results show that TMEM131L corresponds to an evolutionary conserved regulator of the Notch signaling pathway.Entities:
Keywords: Drosophila; Human T cell differentiation; Notch; TMEM131L
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Year: 2017 PMID: 28347816 DOI: 10.1016/j.bbrc.2017.03.123
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575