Ryseck R P, Macdonald-Bravo H, Mattéi M G, Bravo R
Bristol-Myers Squibb Pharmaceutical Research Institute, Department of Molecular Biology, Princeton, New Jersey 08543.
Cell Growth Differ. 1991 May;2(5):225-33.
We have characterized a growth factor-inducible gene, fisp-12, previously isolated by differential screening of a lambda complementary DNA library of RNA from serum-stimulated NIH 3T3 cells, and have shown that it encodes a cysteine-rich secreted protein of 348 amino acids. The induction of fisp-12 mRNA is rapid and remains for at least 8 h at a high level of expression. The increased level of fisp-12 mRNA following serum stimulation is mainly due to transcriptional activation. Studies on the genomic structure reveal that the fisp-12 transcription unit is 3.1 kilobases long and split into five exons. The 5' flanking region does not contain serum-responsive elements normally found in other immediate early genes. Immunoprecipitation analyses show that the protein is rapidly induced following serum stimulation and that it is efficiently secreted in an unglycosylated form to the medium. The fisp-12 gene maps to the [10A3-10B1] region of the murine genome.
我们已对一个生长因子诱导基因fisp - 12进行了特征描述,该基因先前是通过对来自血清刺激的NIH 3T3细胞的λ互补DNA文库进行差异筛选分离得到的,并且已表明它编码一种含有348个氨基酸的富含半胱氨酸的分泌蛋白。fisp - 12 mRNA的诱导迅速,并且在高水平表达下至少持续8小时。血清刺激后fisp - 12 mRNA水平的升高主要是由于转录激活。对基因组结构的研究表明,fisp - 12转录单位长3.1千碱基,分为五个外显子。5'侧翼区域不包含其他立即早期基因中通常存在的血清反应元件。免疫沉淀分析表明,该蛋白在血清刺激后迅速诱导产生,并且它以未糖基化的形式有效地分泌到培养基中。fisp - 12基因定位于小鼠基因组的[10A3 - 10B1]区域。