摘要
转染了P75NGFR的R2神经细胞系R2L1在去血清的培养时可以诱导细胞凋亡的发生.此凋亡可以被RNA合成抑制剂放线菌素D和蛋白质合成抑制剂环己酰胺所抑制.利用DDRT-PCR技术比较了去血清培养的发生凋亡的R2L1细胞与有血清培养的不发生凋亡的R2L1细胞以及去血清培养的不发生凋亡的R2P细胞基因表达的差异.克隆了数个特异或差异表达的短cDNA片段,经Northern杂交证实其中两个片段LIAREST-1和LIAREST-2表达量在凋亡细胞中显著高于不发生凋亡的细胞中,GenBank检索表明此二片段为新的cDNA序列并给予登录号U47315和U47316.另有一个cDNA片段LIARCD-3在凋亡细胞中受到了明显的抑制,经检索为一已知的与前强啡肽原上游调控区结合的DNA结合蛋白cDNA编码区的一部分。
Apoptosis was observed in P 75NGFR expressing R2 cells (R2L1)after depriving serum from the culture medium,but not in PXT 1 transfected control R2 cells (R2P).Differential display technique was used to reveal the differentially expressed genes between normal control and apoptotic neural cells.Several short cDNA fragments were cloned and sequenced.These differentially expressed fragments were further confirmed by Northern blotting hybridization with their original total RNAs.The result showed that there were two of the short cDNA fragments LIAREST 1 and LIAREST 2 whose expression levels in apoptotic serum depriving cultured R2L1 cells were significantly higher than in normal serum containing cultured R2L1 cells and serum depriving cultured R2P cells.Sequence analysis showed that both of them contained a 3'poly A tail and a polyA tail adding signal in the 17 nucleotides upstream from 5' ending of polyA.Another short cDNA fragment LIARCD 3 was observed,whose expression level in apoptotic serum depriving cultured R2L1 cells was 63 4% and 62 3% lower than in serum containing cultured R2L1 cells and serum depriving cultured R2P cells,respectively.The full length of this cDNA fragment was cloned by Gu Jun of NIH in 1994 and is accessible with the accession number U08214.It encodes a protein(UreB 1)binding to an 8 nucleotide upstream regulation element(URE)for a translation initator element in the preprodynorphin promoter,and with a tyrosine kinase phosphorylation consensus.The role of these genes in apoptosis of neural cells in unknown at present.
出处
《中国生物化学与分子生物学报》
CAS
CSCD
1998年第5期610-616,共7页
Chinese Journal of Biochemistry and Molecular Biology
基金
国家自然科学基金
卫生部青年基金