کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6263196 | 1613844 | 2015 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Research ReportCharacterisation of multiple regulatory domains spanning the major transcriptional start site of the FUS gene, a candidate gene for motor neurone disease Research ReportCharacterisation of multiple regulatory domains spanning the major transcriptional start site of the FUS gene, a candidate gene for motor neurone disease](/preview/png/6263196.png)
- cis-acting DNA regulators of FUS gene promoter identified by sequence conservation.
- both evolutionary conserved regions enhance reporter gene expression in culture.
- reporter gene expression is enhanced by ECRs in developing motor neurons in vivo.
- both domains may regulate FUS expression in normal tissue and in ALS.
Fused-In-Sarcoma (FUS) is a candidate gene for neurological disorders including motor neurone disease and Parkinson׳s disease in addition to various types of cancer. Recently it has been reported that over expression of FUS causes motor neurone disease in mouse models hence mutations leading to changes in gene expression may contribute to the development of neurodegenerative disease. Genome evolutionary conservation was used to predict important cis-acting DNA regulators of the FUS gene promoter that direct transcription. The putative regulators identified were analysed in reporter gene assays in cells and in chick embryos. Our analysis indicated in addition to regulatory domains 5Ⲡof the transcriptional start site an important regulatory domain resides in intron 1 of the gene itself. This intronic domain functioned both in cell lines and in vivo in the neural tube of the chick embryo including developing motor neurones. Our data suggest the interaction of multiple domains including intronic domains are involved in expression of FUS. A better understanding of the regulation of expression of FUS may give insight into how its stimulus inducible expression may be associated with neurological disorders.
Journal: Brain Research - Volume 1595, 21 January 2015, Pages 1-9