Molecular and functional characterization of the stress-induced protein (SIP) gene and its two transcripts generated by alternative splicing - SIP induced by stress and promotes cell death

We have used a quantitative fluorescent cDNA microarray hybridization appro ach to identify pancreatic genes induced by the cellular stress promoted by acute pancreatitis in the mouse. We report the cloning and characterizatio n of one of them that encodes the stress-induced proteins (SIP). The mouse SIP gene is organized into five exons and expands over similar to 20 kiloba se pairs. Exon 4 (38 base pairs) is alternatively spliced to generate two t ranscripts. Northern blot and in situ hybridization showed that both SIP mR NAs are rapidly and strongly induced in acinar cells of the pancreas with a cute pancreatitis. They are also constitutively expressed in several other tissues, although with different ratios. They encode proteins of 18 and 27 kDa (SIP18 and SIP27). SIP27 is identical to the thymus-expressed acidic pr otein (TEAP) protein, formerly described as a thymus-specific protein. Expr ession of the SIP18 and SIP27/EGFP or V5 fusion proteins showed that both a re nuclear factors. We monitored SIP expression in NIH3T3 cells submitted t o various stress agents. UV stress, base damaging, mutagenic stress, ethano l, heat shock, and oxidative stress induced the concomitant expression of S IP's and SIP27 mRNAs. Finally, transient transfection of SIP's and SIP27 ex pression plasmids induced death by apoptosis in COS7 cells as measured by t erminal deoxynuelcotidyltransferase-mediated dUTP nick end-labeling stainin g. In conclusion, the SIP gene is an important element of cellular stress r esponse. It is expressed in many tissues and induced by a variety of stress agents affecting many cellular pathways. SIP generates, by alternative spl icing, two nuclear proteins that can promote cell death by apoptosis.