Abstract | INTRODUCTION: METHODS AND RESULTS: Using exome sequencing in a family with three affected brothers, we identified a mutation in the intron 7 splice donor site (c.471+2T→A) of the N- acetyltransferase NAA10 gene. NAA10 has been previously shown to be mutated in patients with Ogden syndrome, which is clinically distinct from LMS. Linkage studies for this family mapped the disease locus to Xq27-Xq28, which was consistent with the locus of NAA10. The mutation co-segregated with the phenotype and cDNA analysis showed aberrant transcripts. Patient fibroblasts lacked expression of full length NAA10 protein and displayed cell proliferation defects. Expression array studies showed significant dysregulation of genes associated with genetic forms of anophthalmia such as BMP4, STRA6, and downstream targets of BCOR and the canonical WNT pathway. In particular, STRA6 is a retinol binding protein receptor that mediates cellular uptake of retinol/ vitamin A and plays a major role in regulating the retinoic acid signalling pathway. A retinol uptake assay showed that retinol uptake was decreased in patient cells. CONCLUSIONS: We conclude that the NAA10 mutation is the cause of LMS in this family, likely through the dysregulation of the retinoic acid signalling pathway.
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Authors | Taraneh Esmailpour, Hamidreza Riazifar, Linan Liu, Sandra Donkervoort, Vincent H Huang, Shreshtha Madaan, Bassem M Shoucri, Anke Busch, Jie Wu, Alexander Towbin, Robert B Chadwick, Adolfo Sequeira, Marquis P Vawter, Guoli Sun, Jennifer J Johnston, Leslie G Biesecker, Riki Kawaguchi, Hui Sun, Virginia Kimonis, Taosheng Huang |
Journal | Journal of medical genetics
(J Med Genet)
Vol. 51
Issue 3
Pg. 185-96
(Mar 2014)
ISSN: 1468-6244 [Electronic] England |
PMID | 24431331
(Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- RNA Splice Sites
- Tretinoin
- N-Terminal Acetyltransferase A
- NAA10 protein, human
- N-Terminal Acetyltransferase E
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Topics |
- Anophthalmos
(genetics, physiopathology)
- Cell Proliferation
- Cells, Cultured
- Female
- Fibroblasts
- Humans
- Male
- Microphthalmos
(genetics, physiopathology)
- Mutation
(genetics)
- N-Terminal Acetyltransferase A
(genetics)
- N-Terminal Acetyltransferase E
(genetics)
- Pedigree
- Phenotype
- RNA Splice Sites
(genetics)
- Signal Transduction
(genetics)
- Tretinoin
(metabolism)
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