RGD Reference Report - Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex. - Rat Genome Database
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Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.

Authors: Pasternack, SM  Refke, M  Paknia, E  Hennies, HC  Franz, T  Schafer, N  Fryer, A  Van Steensel, M  Sweeney, E  Just, M  Grimm, C  Kruse, R  Ferrandiz, C  Nothen, MM  Fischer, U  Betz, RC 
Citation: Pasternack SM, etal., Am J Hum Genet. 2013 Jan 10;92(1):81-7. doi: 10.1016/j.ajhg.2012.10.022. Epub 2012 Dec 13.
RGD ID: 10768831
Pubmed: (View Article at PubMed) PMID:23246290
DOI: Full-text: DOI:10.1016/j.ajhg.2012.10.022

Hypotrichosis simplex (HS) comprises a group of hereditary isolated alopecias that are characterized by a diffuse and progressive loss of hair starting in childhood and shows a wide phenotypic variability. We mapped an autosomal-dominant form of HS to chromosome 1q31.3-1q41 in a Spanish family. By direct sequencing, we identified the heterozygous mutation c.1A>G (p.Met1?) in SNRPE that results in loss of the start codon of the transcript. We identified the same mutation in a simplex HS case from the UK and an additional mutation (c.133G>A [p.Gly45Ser]) in a simplex HS case originating from Tunisia. SNRPE encodes a core protein of U snRNPs, the key factors of the pre-mRNA processing spliceosome. The missense mutation c.133G>A leads to a glycine to serine substitution and is predicted to disrupt the structure of SNRPE. Western blot analyses of HEK293T cells expressing SNRPE c.1A>G revealed an N-terminally truncated protein, and therefore the mutation might result in use of an alternative in-frame downstream start codon. Subcellular localization of mutant SNRPE by immunofluorescence analyses as well as incorporation of mutant SNRPE proteins into U snRNPs was found to be normal, suggesting that the function of U snRNPs in splicing, rather than their biogenesis, is affected. In this report we link a core component of the spliceosome to hair loss, thus adding another specific factor in the complexity of hair growth. Furthermore, our findings extend the range of human phenotypes that are linked to the splicing machinery.


Disease Annotations    
hypotrichosis 1  (IAGP,ISO)

Phenotype Annotations    

Human Phenotype
Alopecia  (IAGP)
Objects Annotated

Genes (Rattus norvegicus)
Snrpe  (small nuclear ribonucleoprotein polypeptide E)

Genes (Mus musculus)
Snrpe  (small nuclear ribonucleoprotein E)

Genes (Homo sapiens)
SNRPE  (small nuclear ribonucleoprotein polypeptide E)

Additional Information