Abe R, Yamamoto K, Sakamoto H
Department of Biology, Faculty of Science, Kobe University, Japan.
Nucleic Acids Res. 1996 Jun 1;24(11):2011-6. doi: 10.1093/nar/24.11.2011.
We have identified cDNAs encoding Mel-N1, the mouse homologue of a human nervous system-specific RNA-binding protein, Hel-N1. Two major mRNA transcripts of Mel-N1 were detected predominantly in the adult mouse brain by Northern blot analysis. To gain insight into the RNA binding specificity of Mel-N1, we performed iterative in vitro RNA selection. The resulting in vitro selected RNAs were found to contain AU-rich sequences as well as a GAAA motif in the majority of clones. By means of in vitro binding assays we demonstrate that this GAAA sequence appears to significantly affect the Mel-N1 RNA-binding efficiency. Our studies further reveal that Mel-N1 can bind to its own 3' untranslated region (3'UTR) as well as to the c-fos 3'UTR, and is localized predominantly in the cytoplasmic region in cells, suggesting that posttranscriptional autoregulation of Mel-N1 gene expression occurs in vivo.
我们已经鉴定出编码Mel-N1的cDNA,它是人类神经系统特异性RNA结合蛋白Hel-N1的小鼠同源物。通过Northern印迹分析,在成年小鼠大脑中主要检测到Mel-N1的两种主要mRNA转录本。为了深入了解Mel-N1的RNA结合特异性,我们进行了迭代体外RNA筛选。结果发现,在大多数克隆中,体外筛选出的RNA含有富含AU的序列以及GAAA基序。通过体外结合试验,我们证明这个GAAA序列似乎显著影响Mel-N1的RNA结合效率。我们的研究进一步表明,Mel-N1可以与其自身的3'非翻译区(3'UTR)以及c-fos 3'UTR结合,并且在细胞中主要定位于细胞质区域,这表明Mel-N1基因表达的转录后自动调节在体内发生。