癌变·畸变·突变 ›› 2008, Vol. 20 ›› Issue (2): 85-088.doi: 10.3969/j.issn.1004-616x.2008.02.002

• 论著 • 上一篇    下一篇

食管癌相关功能未知基因的电子克隆延伸与ncRNA的发现

吴炳礼1,3,许丽艳2,应晓敏3,牛永东1,李伍举3,,李恩民1   

  1. 1. 汕头大学医学院生化与分子生物学教研室,汕头 515041; 2. 汕头大学医学院肿瘤病理研究室,汕头 515041;3.军事医学科学院基础医学研究所,北京 100850
  • 收稿日期:2007-10-25 修回日期:2007-11-10 出版日期:2008-03-30 发布日期:2008-03-30
  • 通讯作者: 李恩民,李伍举

Silicon Cloning for the Unknown Functional Genes Related to Esophageal Carcinoma and ncRNA Finding

WU Bing-li1,3, XU Li-yan2, YING Xiao-min3,NIU Yong-dong1, LI Wu-ju3,, LI En-min1   

  1. 1. Biochemistry and Molecular Biology Department, Medical College of Shantou University,Shantou 515041; 2. Department of Tumor Pathology, Medical College of Shantou University, Shantou 515041; 3. Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100850,China
  • Received:2007-10-25 Revised:2007-11-10 Online:2008-03-30 Published:2008-03-30
  • Contact: LI En-min,LI Wu-ju

摘要: 背景与目的: 运用电子克隆等生物信息学方法研究筛查出的48个与食管癌相关功能未知的DNA序列片段,为食管癌相关研究提供指导。 材料与方法: 以48个DNA序列片段为核心,运用BioEdit建立本地数据库;通过电子克隆的方法对48个DNA序列中功能未知的基因片段进行序列延伸;通过BLAST同源分析搜索48个基因的内含子以及上下游基因间隔区中存在的非编码RNA(noncoding RNA,ncRNA)。 结果: 48个DNA序列中功能未知的基因片段通过电子克隆的方法平均能够延伸190 bp以上;在48个基因的内含子以及上下游基因间隔区存在着与已知ncRNA相似性很高的片段。 结论: 运用电子克隆的方法可以使某些食管癌相关功能未知基因的序列得以明显延伸;一些食管癌相关基因所在的染色体区段存在着某些与ncRNA高度相似的片段,这提示我们,ncRNA可能参与食管癌的发生过程,其具体功能有待深入研究。

关键词: 生物信息学, 序列分析, 非编码RNA, 电子克隆

Abstract: BACKGROUND AND AIM: In order to provide further support for the experimental verification and functional exploration of 48 DNA sequences related to esophageal carcinoma found in our lab, these sequences were investigated systematically using bioinformatics methods such as silicon cloning and BLAST search tool. MATERIALS AND METHODS: A local database including the 48 sequences was constructed by the BioEdit software; the 48 DNA sequences coding unknown genes were extended by the method of silicon cloning; the potential ncRNAs, located in the introns, the upstream and downstream of intergenic regions of the above 48 DNA sequences, were analyzed by BLAST tool. RESULTS: The sequences coding unknown genes were extended to more than 190 bp on average using silicon cloning. Some sequence segments with high similarity to the known noncoding RNA(ncRNAs) were found in the intronic or intergenic regions. CONCLUSION: Some esophageal carcinoma related genes can be extended obviously by the method of silicon cloning,some sequences with high similarity to known ncRNAs were found in the chromosome region where the esophageal carcinoma related genes are located. The information gives us potential clues that these ncRNAs maybe participate in the development process of esophageal carcinoma, and the functions of these ncRNAs needs further study.

Key words: bioinformatics, sequence analysis, noncoding RNA, silicon cloning