A novel essential splice site variant in SPTB in a large hereditary spherocytosis family
In: Molecular Genetics & Genomic Medicine Molecular Genetics & Genomic Medicine, Jg. 9 (2021), Heft 5, S. n/a-n/a
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Zugriff:
Background We studied a large family with 22 individuals affected with autosomal dominant hereditary spherocytosis (HS). Methods Genome‐wide linkage, whole‐genome sequencing (WGS), Sanger sequencing, RT‐PCR, and ToPO TA cloning analyses were performed. Results We revealed a heterozygous G>A transition in the 14q23 locus, at position +1 of the intron 8 donor splice site of the spectrin beta, erythrocytic (SPTB) gene. This splice variant (SPTB c.1064+1G>A) was confirmed by Sanger sequencing and showed complete co‐segregation with HS in the family. Further RT‐PCR reactions and sequencing analysis indicated that the variant leads to the exclusion of exon 8 and subsequent frameshift in exon 9 and a premature stop codon in SPTB. Translation of the altered allele would lead to a truncation with a loss of all spectrin repeat domains in SPTB protein. Conclusion This variant is novel and has not been found in any databases. We propose that this splice variant explains the spherocytosis phenotype observed in this large family.
We studied a large family with 22 individuals affected with autosomal dominant hereditary spherocytosis (HS). Genome‐wide linkage and whole‐genome sequencing analyses revealed a heterozygous G>A transition in the 14q23 locus, at position +1 of the intron 8 donor splice site of the spectrin beta, erythrocytic (SPTB) gene.
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A novel essential splice site variant in SPTB in a large hereditary spherocytosis family
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Autor/in / Beteiligte Person: | Brock, Pamela ; Nieminen, Taina T. ; He, Huiling ; Wang, Yanqiang ; Comiskey, Daniel F. ; Hendrickson, Isabella V. ; Li, W. G. ; Liyanarachchi, Sandya ; Albert de la Chapelle ; Department of Medical and Clinical Genetics ; Biosciences |
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Zeitschrift: | Molecular Genetics & Genomic Medicine Molecular Genetics & Genomic Medicine, Jg. 9 (2021), Heft 5, S. n/a-n/a |
Veröffentlichung: | 2021 |
Medientyp: | unknown |
ISSN: | 2324-9269 (print) |
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