An investigation of NFXL1, a gene implicated in a study of specific language impairment. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Nudel, Ron
• Is Part Of: Journal of neurodevelopmental disorders. Volume 8:Issue 1(2016)
• Page Start: 1
• Page End: 5
• Publication Date: 2016-12
• Subjects: Specific language impairment -- NFXL1 -- Neurogenetics -- Neurodevelopment -- Language disorder -- Transcription factor -- Cerebellum; Developmental neurobiology -- Periodicals; Neurosciences -- Periodicals; Nervous system -- Diseases -- Periodicals; 618.928
• DOI: 10.1186/s11689-016-9146-9
• Languages: English
• ISSNs: 1866-1947

Abstract

Abstract Background A recent study identifiedNFXL1 as a candidate gene for specific language impairment. The protein encoded by this gene is predicted to be a transcription factor based on domain similarities with NFX1, a repressor of HLA class II genes, which have themselves been implicated in specific language impairment. However, there is very little literature on the function ofNFXL1 . Methods This report describes a study ofNFXL1 expression in several human tissues and an investigation of differential expression in several specific brain regions through quantitative PCR as well as a study of the protein's sub-cellular localization in HEK cells and SH-SY5Y cells through immunofluorescence. Results TheNFXL1 transcript was found in all investigated tissues. In the brain, a high level ofNFXL1 expression was found in the cerebellum. An analysis of the sub-cellular localization of the protein showed a cytoplasmic pattern in the investigated cells. Conclusions TheNFXL1 transcript was present in samples from different tissues; in the brain, a high expression level was found in a region implicated in some language-related pathologies. NFXL1 did not show nuclear localization, suggesting that, if it regulates transcription, certain conditions may be required for it to translocate to the nucleus.