PUBLICATION
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis
- Authors
- DeLuca, A.P., Whitmore, S.S., Barnes, J., Sharma, T.P., Westfall, T.A., Scott, C.A., Weed, M.C., Wiley, J.S., Wiley, L.A., Johnston, R.M., Schnieders, M.J., Lentz, S.R., Tucker, B.A., Mullins, R.F., Scheetz, T.E., Stone, E.M., Slusarski, D.C.
- ID
- ZDB-PUB-151024-2
- Date
- 2016
- Source
- Human molecular genetics 25(1): 44-56 (Journal)
- Registered Authors
- Slusarski, Diane C.
- Keywords
- none
- MeSH Terms
-
- Adolescent
- Animals
- Carrier Proteins
- Cells, Cultured
- Exome
- Gene Expression
- Humans
- Male
- Mutation
- Nucleotides/metabolism
- Nucleotidyltransferases/genetics*
- Perilipin-1
- Phosphoproteins
- RNA Splicing
- Retinitis Pigmentosa/genetics*
- Sequence Analysis, DNA
- Young Adult
- Zebrafish
- PubMed
- 26494905 Full text @ Hum. Mol. Genet.
Citation
DeLuca, A.P., Whitmore, S.S., Barnes, J., Sharma, T.P., Westfall, T.A., Scott, C.A., Weed, M.C., Wiley, J.S., Wiley, L.A., Johnston, R.M., Schnieders, M.J., Lentz, S.R., Tucker, B.A., Mullins, R.F., Scheetz, T.E., Stone, E.M., Slusarski, D.C. (2016) Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Human molecular genetics. 25(1):44-56.
Abstract
Retinitis Pigmentosa (RP) is a highly heterogeneous group of disorders characterized by degeneration of the retinal photoreceptor cells and progressive loss of vision. While hundreds of mutations in more than 100 genes have been reported to cause RP, discovering the causative mutations in many patients remains a significant challenge. Exome sequencing in an individual affected with non-syndromic RP revealed two plausibly-disease-causing variants in TRNT1, a gene encoding a nucleotidyltransferase critical for tRNA processing. Seven hundred twenty-seven additional unrelated individuals with molecularly uncharacterized RP were completely screened for TRNT1 coding sequence variants and a second family was identified with two members who exhibited a phenotype that was remarkably similar to the index patient. Inactivating mutations in TRNT1 have been previously shown to cause a severe congenital syndrome of sideroblastic anemia, B-cell immunodeficiency, recurrent fevers and developmental delay (SIFD). Complete blood counts of all three of our patients revealed red blood cell microcytosis and anisocytosis with only mild anemia. Characterization of TRNT1 in patient-derived cell lines revealed reduced but detectable TRNT1 protein, consistent with partial function. Suppression of trnt1 expression in zebrafish recapitulated several features of the human SIFD syndrome, including anemia and sensory organ defects. When levels of trnt1 were titrated visual dysfunction was found in the absence of other phenotypes. The visual defects in the trnt1 knockdown zebrafish were ameliorated by the addition of exogenous human TRNT1 RNA. Our findings indicate that hypomorphic TRNT1 mutations can cause a recessive disease that is almost entirely limited to the retina.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping