生物
遗传学
疾病基因鉴定
外显子组测序
基因
桑格测序
甲基化
甲基转移酶
无意义介导的衰变
胡说
突变
RNA剪接
核糖核酸
作者
Marie Bernkopf,Gerald Webersinke,Chanakan Tongsook,Chintan N. Koyani,Muhammad Rafiq,Muhammad Ayaz,Doris H. Müller,Christian Enzinger,Muhammad Aslam,Farooq Naeem,Kurt Schmidt,Karl Gruber,Michael R. Speicher,Ernst Malle,Peter Macheroux,Muhammad Ayub,John B. Vincent,Christian Windpassinger,Peter E. Newburger
摘要
We describe the characterization of a gene for mild nonsyndromic autosomal recessive intellectual disability (ID) in two unrelated families, one from Austria, the other from Pakistan. Genome-wide single nucleotide polymorphism microarray analysis enabled us to define a region of homozygosity by descent on chromosome 17q25. Whole-exome sequencing and analysis of this region in an affected individual from the Austrian family identified a 5 bp frameshifting deletion in the METTL23 gene. By means of Sanger sequencing of METTL23, a nonsense mutation was detected in a consanguineous ID family from Pakistan for which homozygosity-by-descent mapping had identified a region on 17q25. Both changes lead to truncation of the putative METTL23 protein, which disrupts the predicted catalytic domain and alters the cellular localization. 3D-modelling of the protein indicates that METTL23 is strongly predicted to function as an S-adenosyl-methionine (SAM)-dependent methyltransferase. Expression analysis of METTL23 indicated a strong association with heat shock proteins, which suggests that these may act as a putative substrate for methylation by METTL23. A number of methyltransferases have been described recently in association with ID. Disruption of METTL23 presented here supports the importance of methylation processes for intact neuronal function and brain development.
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