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Publication Type : Journal Article
Thematic Areas : Medical Sciences
Publisher : American Journal of Human Genetics
Source : American Journal of Human Genetics, Volume 87, Number 2, p.189-198 (2010)
Keywords : Abnormalities, adolescent, adult, allele, Alleles, article, Base Sequence, bone demineralization, bone development, brain development, child, Chromosomes, codon, comparative genomic hybridization, DNA Mutational Analysis, embryo, facies, failure to thrive, female, fetus, frameshift mutation, gene deletion, Gene Expression Regulation, gene mutation, Genetic Testing, human, human tissue, Humans, In Situ Hybridization, kyphoscoliosis, major clinical study, male, malformation syndrome, marshall smith syndrome, Messenger, Molecular Sequence Data, mouse, Multiple, Mus, Mutation, newborn, NFI Transcription Factors, nonhuman, Nonsense, nonsense mediated mRNA decay, nuclear factor, nuclear factor I, nuclear factor ix, osteopenia, Pair 19, phenotype, priority journal, protein expression, protein function, respiratory failure, Reverse Transcriptase Polymerase Chain Reaction, RNA, RNA splicing, RNA Stability, Sotos syndrome, spine malformation, Syndrome, unclassified drug, weight gain
Campus : Kochi
School : School of Medicine
Department : Paediatrics
Year : 2010
Abstract : By using a combination of array comparative genomic hybridization and a candidate gene approach, we identified nuclear factor I/X (NFIX) deletions or nonsense mutation in three sporadic cases of a Sotos-like overgrowth syndrome with advanced bone age, macrocephaly, developmental delay, scoliosis, and unusual facies. Unlike the aforementioned human syndrome, Nfix-deficient mice are unable to gain weight and die in the first 3 postnatal weeks, while they also present with a spinal deformation and decreased bone mineralization. These features prompted us to consider NFIX as a candidate gene for Marshall-Smith syndrome (MSS), a severe malformation syndrome characterized by failure to thrive, respiratory insufficiency, accelerated osseous maturation, kyphoscoliosis, osteopenia, and unusual facies. Distinct frameshift and splice NFIX mutations that escaped nonsense-mediated mRNA decay (NMD) were identified in nine MSS subjects. NFIX belongs to the Nuclear factor one (NFI) family of transcription factors, but its specific function is presently unknown. We demonstrate that NFIX is normally expressed prenatally during human brain development and skeletogenesis. These findings demonstrate that allelic NFIX mutations trigger distinct phenotypes, depending specifically on their impact on NMD. © 2010 The American Society of Human Genetics.
Cite this Research Publication : Va Malan, Rajan, Db, Thomas, Sa, Shaw, A. Cc, Picard, HaLouis Dit, Layet, Vd, Till, Me, Van Haeringen, Af, Mortier, Gg, Nampoothiri, Sh, Pušeljić, Si, Legeai-Mallet, La, Carter, N. Pb, Vekemans, Ma, Munnich, Aa, Hennekam, R. Cj, Colleaux, La, and Cormier-Daire, Va, “Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a sotos-like or a Marshall-Smith Syndrome”, American Journal of Human Genetics, vol. 87, pp. 189-198, 2010.