Vasseur S, Vidal Mallo G, Fiedler F, Bödeker H, Cánepa E, Moreno S, Iovanna J L
U.315 INSERM, Marseille, France.
Eur J Biochem. 1999 Feb;259(3):670-5. doi: 10.1046/j.1432-1327.1999.00092.x.
We have previously identified a new rat mRNA, provisionally named p8, which showed a strong, but transient, induction in the pancreas in response to acute pancreatitis. We report here the cloning and sequencing of the human p8 cDNA. The human p8 polypeptide is 82 amino acids long and shows an overall identity of 74% with the rat counterpart. The complete structure of the p8 gene was also established. The p8 gene comprises three exons separated by two introns and the gene was mapped to chromosome 16. Analysis of the p8 primary structure suggested the presence of a bipartite motif of nuclear targeting, indicating that p8 may function within the nucleus. This presumption has been confirmed by transfection of COS-7 cells with the p8 cDNA followed by immunostaining with specific antibodies. p8 mRNA expression is induced in some, but not all, cells by serum starvation and ceramide. To analyze the p8 function, we stably transfected HeLa cells with a p8 expression plasmid, and measured their growth and their sensitivity to apoptosis. Response to TNF alpha and staurosporine-induced apoptosis was not modified by p8 expression. However, cells expressing p8 grew significantly more rapidly.
我们之前鉴定出一种新的大鼠mRNA,暂命名为p8,它在胰腺中对急性胰腺炎有强烈但短暂的诱导表达。我们在此报告人p8 cDNA的克隆和测序。人p8多肽长82个氨基酸,与大鼠对应物的总体同一性为74%。还确定了p8基因的完整结构。p8基因由三个外显子和两个内含子分隔,该基因定位于16号染色体。对p8一级结构的分析表明存在核靶向的双分基序,这表明p8可能在细胞核内发挥作用。用p8 cDNA转染COS-7细胞,然后用特异性抗体进行免疫染色,证实了这一推测。血清饥饿和神经酰胺可在部分而非所有细胞中诱导p8 mRNA表达。为分析p8的功能,我们用p8表达质粒稳定转染HeLa细胞,并检测其生长情况和对凋亡的敏感性。p8表达未改变对TNFα和星形孢菌素诱导凋亡的反应。然而,表达p8的细胞生长明显更快。