Trim71/lin-41 Links an Ancient miRNA Pathway to Human Congenital Hydrocephalus
Document Type
Article
Abstract
Tripartite motif 71 (Trim71)/lineage defective 41 (lin-41) is the primary target of the ancient lethal 7 (let-7) miRNA that is essential for survival and development across animal phylogeny. Recent work identified Trim71 as a critical regulator of mammalian neural stem cell (NSC) fate and a bona fide human disease gene in congenital hydrocephalus (CH). Studying TRIM71 as a paradigm of NSC involvement in CH is a remarkable opportunity to better understand the mechanisms that regulate the timing of brain development and the pathogenesis of the most common pediatric neurosurgical disorder.
Medical Subject Headings
Brain (abnormalities, embryology, metabolism); Genetic Predisposition to Disease; Humans; Hydrocephalus (diagnosis, genetics); MicroRNAs (genetics); Neural Stem Cells (metabolism); Neurogenesis (genetics); Transcription Factors (genetics); Tripartite Motif Proteins (genetics); Ubiquitin-Protein Ligases (genetics)
Publication Date
6-1-2019
Publication Title
Trends in molecular medicine
E-ISSN
1471-499X
Volume
25
Issue
6
First Page
467
Last Page
469
PubMed ID
30975633
Digital Object Identifier (DOI)
10.1016/j.molmed.2019.03.004
Recommended Citation
Duy, Phan Q.; Furey, Charuta G.; and Kahle, Kristopher T., "Trim71/lin-41 Links an Ancient miRNA Pathway to Human Congenital Hydrocephalus" (2019). Neurosurgery. 2414.
https://scholar.barrowneuro.org/neurosurgery/2414