JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.

Nat Genet 2014 Sep 17;46(9):1021-7. Epub 2014 Aug 17.

Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig Maximilians University, Munich, Germany.

The analysis of individuals with severe congenital neutropenia (SCN) may shed light on the delicate balance of factors controlling the differentiation, maintenance and decay of neutrophils. We identify 9 distinct homozygous mutations in the JAGN1 gene encoding Jagunal homolog 1 in 14 individuals with SCN. JAGN1-mutant granulocytes are characterized by ultrastructural defects, a paucity of granules, aberrant N-glycosylation of multiple proteins and increased incidence of apoptosis. JAGN1 participates in the secretory pathway and is required for granulocyte colony-stimulating factor receptor-mediated signaling. JAGN1 emerges as a factor that is necessary in the differentiation and survival of neutrophils.

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http://dx.doi.org/10.1038/ng.3069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829076PMC
September 2014
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