Castillo S O, Xiao Q, Lyu M S, Kozak C A, Nikodem V M
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-1766, USA.
Genomics. 1997 Apr 15;41(2):250-7. doi: 10.1006/geno.1997.4677.
We have cloned and characterized the organization of the mouse orphan nuclear receptor Nurr1 gene. The Nurr1 gene is approximately 7 kb long, contains eight exons and seven introns, and mapped to mouse chromosome 2. Although the exon/intron structure of Nurr1 is nearly identical to that of Nur77, Nurr1 possesses an additional untranslated exon. Primer extension was used to identify two major transcription initiation sites mapped 37 nucleotides apart in the first untranslated exon. Functional studies of chimeric Nurr1-luciferase reporter genes delineated the promoter region and underscored the importance of the +1 transcription start site. Sequence analysis of the 5' flanking region surrounding +1 revealed several possible response elements such as a hexanucleotide glucocorticoid binding site, a cAMP-response element, a CArG box, and two c-Jun-binding sites. These data help to explain the different response characteristics of two closely related early response genes, Nurr1 and Nur77.
我们已经克隆并鉴定了小鼠孤儿核受体Nurr1基因的结构。Nurr1基因长度约为7kb,包含8个外显子和7个内含子,定位于小鼠2号染色体。虽然Nurr1的外显子/内含子结构与Nur77几乎相同,但Nurr1有一个额外的非翻译外显子。采用引物延伸法在第一个非翻译外显子中鉴定出两个主要转录起始位点,它们相距37个核苷酸。对嵌合Nurr1 - 荧光素酶报告基因的功能研究确定了启动子区域,并强调了+1转录起始位点的重要性。对+1周围5'侧翼区域的序列分析揭示了几个可能的反应元件,如六核苷酸糖皮质激素结合位点、cAMP反应元件、CArG框和两个c - Jun结合位点。这些数据有助于解释两个密切相关的早期反应基因Nurr1和Nur77的不同反应特征。