Xiang Bo, Wang Wei, Yi Mei, Li Wenjuan, Zhou Ming, Li Xiaoling, Li Guiyuan
Cancer Research Institute, Central South University, Changsha 410078, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jul;36(7):597-603. doi: 10.3969/j.issn.1672-7347.2011.07.003.
To analyze the distribution and subcellular localization of NOR1 alternative splice isoforms in human tissues and cell lines.
NOR1 open reading frame(ORF) was amplified from human fetal brain cDNA library and subcloned into pCMV/myc vector. The level of NOR1 mRNA in human tissues was determined by real-time RT-PCR. Region spanning exon 2 was amplified from cDNA or genomic DNA by specific primers and sequenced. The expression plasmids of NOR1 were transfected into cells and immunofluoresence assay was performed to determine the subcellular localization of NOR1 protein isoforms in human cells.
The expression of NOR1 mRNA was high in human adult testis, moderate in human fetus nasopharynx, trachea, brain, and kidney tissues, and weak or undetectable in other tissues. Two splice variants of human NOR1 gene resulted from alternative splicing at exon 2 were identified. Both of isoform 1 and isoform 2 mRNA were detected in human fetus brain. Isoform 2 was the sole isoform in other tissues but brain. Only isoform 2 mRNA was detected in cell lines used in this study, though no genomic deletion of exon 2 could be found in all these cell lines. Immunofluoresence assay showed both isoform 1 and isoform 2 proteins were distributed in cytoplasm.
Alternative splice isoforms of tumor suppressor gene NOR1 are identified. NOR1 isoform 1 and isoform 2 are both detected in fetus brain. NOR1 isoform 2 lacking of exon 2 is the sole isoform in multiple tissues except for brain. The exon 2 encoded peptide does not affect the subcellular location of NOR1 protein.
分析人组织和细胞系中NOR1可变剪接异构体的分布及亚细胞定位。
从人胎脑cDNA文库中扩增NOR1开放阅读框(ORF),并亚克隆至pCMV/myc载体。采用实时逆转录聚合酶链反应(RT-PCR)测定人组织中NOR1 mRNA水平。用特异性引物从cDNA或基因组DNA中扩增跨越外显子2的区域并测序。将NOR1表达质粒转染至细胞中,进行免疫荧光测定以确定人细胞中NOR1蛋白异构体的亚细胞定位。
NOR1 mRNA在成人睾丸中表达较高,在胎儿鼻咽、气管、脑和肾组织中表达中等,在其他组织中表达较弱或未检测到。鉴定出人类NOR1基因由于外显子2处的可变剪接产生的两种剪接变体。在胎儿脑中检测到异构体1和异构体2的mRNA。异构体2是除脑以外其他组织中的唯一异构体。在本研究使用的细胞系中仅检测到异构体2的mRNA,尽管在所有这些细胞系中均未发现外显子2的基因组缺失。免疫荧光测定显示异构体1和异构体2蛋白均分布于细胞质中。
鉴定出肿瘤抑制基因NOR1的可变剪接异构体。在胎儿脑中同时检测到NOR1异构体1和异构体2。缺乏外显子2的NOR1异构体2是除脑以外多个组织中的唯一异构体。外显子2编码的肽不影响NOR1蛋白的亚细胞定位。