Schreiber M, Poirier C, Franchi A, Kurzbauer R, Guenet J L, Carle G F, Wagner E F
Research Institute of Molecular Pathology (IMP), Vienna, Austria.
Oncogene. 1997 Sep 4;15(10):1171-8. doi: 10.1038/sj.onc.1201460.
We have determined the genomic structure of the mouse fra-1 gene, which consists of four exons and three introns at positions also found in the other members of the fos gene family. Fra-1 is expressed rather highly in the brain and testes of adult mice, and at low levels in most other tissues. Absence of c-Fos leads to significantly reduced serum stimulation of fra-1 expression in gene targeted mouse fibroblasts, demonstrating that mitogen induction of fra-1 is partially mediated by c-Fos/AP-1. A polymorphic (CA)n microsatellite marker was found in intron 2 of fra-1 and used to map the gene to the centromeric region of mouse chromosome 19. Since fra-1 maps to the same genomic region as oc (osteosclerosis), an autosomal recessive disorder leading to the bone remodelling disease osteopetrosis, we tested it as a candidate gene for oc. The segregation of fra-1 in two different crosses of mice carrying oc and an allelism test between oc and a targeted disruption of fra-1 demonstrate that fra-1 and oc are two distinct genes rather than oc being a mutant allele of fra-1.
我们已经确定了小鼠fra-1基因的基因组结构,该基因由四个外显子和三个内含子组成,其位置也存在于fos基因家族的其他成员中。Fra-1在成年小鼠的大脑和睾丸中表达相当高,而在大多数其他组织中表达水平较低。在基因靶向的小鼠成纤维细胞中,c-Fos的缺失导致血清对fra-1表达的刺激显著降低,这表明fra-1的丝裂原诱导部分由c-Fos/AP-1介导。在fra-1的内含子2中发现了一个多态性(CA)n微卫星标记,并用于将该基因定位到小鼠19号染色体的着丝粒区域。由于fra-1与oc(骨硬化症)位于同一基因组区域,oc是一种导致骨重塑疾病骨石化症的常染色体隐性疾病,我们将其作为oc的候选基因进行了测试。fra-1在携带oc的小鼠的两个不同杂交中的分离以及oc与fra-1靶向破坏之间的等位性测试表明,fra-1和oc是两个不同的基因,而不是oc是fra-1的突变等位基因。