摘要
目的:研究在口腔癌细胞中剪切因子hnRNP L对其新的靶基因CD55的内含子7的可变剪切的调控作用。方法::应用GEO2R在线软件对GEO数据库中的关于hnRNP L沉默后细胞前体mRNA可变剪切改变的外显子阵列数据进行再分析,发现了一系列hnRNP L的新靶基因,然后在人口腔鳞状细胞癌细胞系CAL 27中应用RNA干扰技术降低hnRNP L的表达,通过逆转录PCR检测CD55内含子7的可变剪切。结果:对外显子阵列数据再分析发现CD55是hnRNP L的靶基因。在CAL 27细胞中抑制hnRNP L的表达时,促进了包含内含子7的CD55亚型的表达。结论:CD55内含子7的保留受到hnRNP L的调控。CD55是hnRNP L在口腔癌细胞中的靶基因。
Objective:To study the effect of splicing factor hnRNP L on alternative splicing of CD55 intron 7,a new target of hnRNP L in CAL 27 cells.Methods:An exon array data about hnRNP L down-regulation in cells in GEO database was re-analyzed with GEO2 Ronline service.HnRNP L was knocked down by using siRNA in oral squamous cell carcinoma(OSCC)CAL 27 cells.Alternative splicing of CD55 intron 7was analyzed by RT-PCR.Results:CD55is a new target of hnRNP L.Knockdown of hnRNP L in CAL 27 cells significantly increased the inclusion of CD55 intron 7.Conclusion:The retention of CD55 intron 7was regulated by hnRNP L.CD55 was the target of hnRNP L in OSCC cells.
作者
张偲
刘苗苗
刘佩琦
贾荣
郭继华
ZHANG Si LIU Miao-miao LIU Pei- qi JIA Rong GUO Ji- hua(The State Key Laboratory Breeding Base of Basic Science of Stomatology ( Hubei- MOST) and Key'Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan 430079, China Department of Endodontics, Hubei- MOST KLOS & KLOBME , School & Hospital of Stomatology , Wuhan University, Wuhan 430079, China.)
出处
《口腔医学研究》
CAS
CSCD
北大核心
2016年第10期1006-1009,共4页
Journal of Oral Science Research
基金
国家自然科学基金(编号:81470741)