iRNA-AI: identifying the adenosine to inosine editing sites in RNA sequences

被引:188
作者
Chen, Wei [1 ,2 ,5 ]
Feng, Pengmian [3 ]
Yang, Hui [4 ]
Ding, Hui [4 ]
Lin, Hao [4 ,5 ]
Chou, Kuo-Chen [4 ,5 ]
机构
[1] North China Univ Sci & Technol, Sch Sci, Dept Phys, Tangshan, Tangshan, Peoples R China
[2] North China Univ Sci & Technol, Ctr Genom & Computat Biol, Tangshan, Tangshan, Peoples R China
[3] North China Univ Sci & Technol, Sch Publ Hlth, Hebei Prov Key Lab Occupat Hlth & Safety Coal Ind, Tangshan, Peoples R China
[4] Univ Elect Sci & Technol China, Ctr Informat Biol, Sch Life Sci & Technol, Minist Educ,Key Lab Neuroinformat, Chengdu, Peoples R China
[5] Gordon Life Sci Inst, Belmont, MA 02478 USA
基金
中国博士后科学基金;
关键词
A-to-I editing; nucleotide chemical properties; nucleotide density distribution; PseKNC; web-server; AMINO-ACID-COMPOSITION; PSEUDO NUCLEOTIDE COMPOSITION; LABEL LEARNING CLASSIFIER; MEMBRANE-PROTEIN TYPES; K-TUPLE; ENSEMBLE CLASSIFIER; SUBCELLULAR-LOCALIZATION; PHYSICOCHEMICAL PROPERTIES; N-6-METHYLADENOSINE SITES; RECOMBINATION SPOTS;
D O I
10.18632/oncotarget.13758
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Catalyzed by adenosine deaminase (ADAR), the adenosine to inosine (A-to-I) editing in RNA is not only involved in various important biological processes, but also closely associated with a series of major diseases. Therefore, knowledge about the A-to-I editing sites in RNA is crucially important for both basic research and drug development. Given an uncharacterized RNA sequence that contains many adenosine (A) residues, can we identify which one of them can be of A-to-I editing, and which one cannot? Unfortunately, so far no computational method whatsoever has been developed to address such an important problem based on the RNA sequence information alone. To fill this empty area, we have proposed a predictor called iRNA-AI by incorporating the chemical properties of nucleotides and their sliding occurrence density distribution along a RNA sequence into the general form of pseudo nucleotide composition (PseKNC). It has been shown by the rigorous jackknife test and independent dataset test that the performance of the proposed predictor is quite promising. For the convenience of most experimental scientists, a user-friendly webserver for iRNA-AI has been established at http://lin.uestc.edu.cn/server/iRNA-AI/, by which users can easily get their desired results without the need to go through the mathematical details.
引用
收藏
页码:4208 / 4217
页数:10
相关论文
共 108 条
[21]   QUASI-CONTINUUM MODELS OF TWIST-LIKE AND ACCORDION-LIKE LOW-FREQUENCY MOTIONS IN DNA [J].
CHOU, KC ;
MAGGIORA, GM ;
MAO, B .
BIOPHYSICAL JOURNAL, 1989, 56 (02) :295-305
[22]   Prediction of membrane protein types by incorporating amphipathic effects [J].
Chou, KC ;
Cai, YD .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2005, 45 (02) :407-413
[23]   Using amphiphilic pseudo amino acid composition to predict enzyme subfamily classes [J].
Chou, KC .
BIOINFORMATICS, 2005, 21 (01) :10-19
[24]   Using functional domain composition and support vector machines for prediction of protein subcellular location [J].
Chou, KC ;
Cai, YD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (48) :45765-45769
[25]   Prediction of signal peptides using scaled window [J].
Chou, KC .
PEPTIDES, 2001, 22 (12) :1973-1979
[26]   COLLECTIVE MOTION IN DNA AND ITS ROLE IN DRUG INTERCALATION [J].
CHOU, KC ;
MAO, BY .
BIOPOLYMERS, 1988, 27 (11) :1795-1815
[27]   LOW-FREQUENCY VIBRATIONS OF DNA-MOLECULES [J].
CHOU, KC .
BIOCHEMICAL JOURNAL, 1984, 221 (01) :27-31
[29]   PREDICTION OF PROTEIN STRUCTURAL CLASSES [J].
CHOU, KC ;
ZHANG, CT .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 30 (04) :275-349
[30]   DIAGRAMMATIZATION OF CODON USAGE IN 339 HUMAN-IMMUNODEFICIENCY-VIRUS PROTEINS AND ITS BIOLOGICAL IMPLICATION [J].
CHOU, KC ;
ZHANG, CT .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1992, 8 (12) :1967-1976