Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Proc Natl Acad Sci U S A. 2011 Jul 26;108(30):12390-5. doi: 10.1073/pnas.1107103108. Epub 2011 Jul 6.
Here we report a human intellectual disability disease locus on chromosome 14q31.3 corresponding to mutation of the ZC3H14 gene that encodes a conserved polyadenosine RNA binding protein. We identify ZC3H14 mRNA transcripts in the human central nervous system, and we find that rodent ZC3H14 protein is expressed in hippocampal neurons and colocalizes with poly(A) RNA in neuronal cell bodies. A Drosophila melanogaster model of this disease created by mutation of the gene encoding the ZC3H14 ortholog dNab2, which also binds polyadenosine RNA, reveals that dNab2 is essential for development and required in neurons for normal locomotion and flight. Biochemical and genetic data indicate that dNab2 restricts bulk poly(A) tail length in vivo, suggesting that this function may underlie its role in development and disease. These studies reveal a conserved requirement for ZC3H14/dNab2 in the metazoan nervous system and identify a poly(A) RNA binding protein associated with a human brain disorder.
在这里,我们报告了一个位于染色体 14q31.3 的人类智力残疾疾病基因座,该基因座对应于 ZC3H14 基因的突变,该基因编码一种保守的多聚腺苷酸 RNA 结合蛋白。我们在人类中枢神经系统中鉴定出 ZC3H14 mRNA 转录本,并且发现啮齿动物 ZC3H14 蛋白在海马神经元中表达,并与神经元胞体中的多聚(A)RNA 共定位。通过突变编码 ZC3H14 同源物 dNab2 的基因创建的这种疾病的果蝇模型也表明,dNab2 对发育至关重要,并且在神经元中对于正常运动和飞行是必需的。生化和遗传数据表明,dNab2 在体内限制多聚(A)尾巴的长度,这表明该功能可能是其在发育和疾病中的作用基础。这些研究揭示了 ZC3H14/dNab2 在后生动物神经系统中的保守需求,并确定了与人类大脑紊乱相关的多聚(A)RNA 结合蛋白。