Knowledge in the investigation of A-to-I RNA editing signals

被引:14
|
作者
Nigita, Giovanni [1 ]
Alaimo, Salvatore [2 ]
Ferro, Alfredo [3 ]
Giugno, Rosalba [3 ]
Pulvirenti, Alfredo [3 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Univ Catania, Dept Math & Comp Sci, Catania, Italy
[3] Univ Catania, Dept Clin & Expt Med, Via Santa Sofia 78, I-95122 Catania, Italy
关键词
A-to-I RNA editing; motif analysis; prediction; ADARs; logistic regression;
D O I
10.3389/fbioe.2015.00018
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA editing is a post-transcriptional alteration of RNA sequences that is able to affect protein structure as well as RNA and protein expression. Adenosine-to-inosine (A-to-I) RNA editing is the most frequent and common post-transcriptional modification in human, where adenosine (A) deamination produces its conversion into inosine (I), which in turn is interpreted by the translation and splicing machineries as guanosine (G). The disruption of the editing machinery has been associated to various human diseases such as cancer or neurodegenerative diseases. This biological phenomenon is catalyzed by members of the adenosine deaminase acting on RNA (ADAR) family of enzymes and occurs on dsRNA structures. Despite the enormous efforts made in the last decade, the real biological function underlying such a phenomenon, as well as ADAR's substrate features still remain unknown. In this work, we summarize the major computational aspects of predicting and understanding RNA editing events. We also investigate the detection of short motif sequences potentially characterizing RNA editing signals and the use of a logistic regression technique to model a predictor of RNA editing events. The latter, named AIRlINER, an algorithmic approach to assessment of A-to-I RNA editing sites in non-repetitive regions, is available as a web app at: http://alpha.dmi.unict.it/airliner/. Results and comparisons with the existing methods encourage our findings on both aspects.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] The majority of A-to-I RNA editing is not required for mammalian homeostasis
    Chalk, Alistair M.
    Taylor, Scott
    Heraud-Farlow, Jacki E.
    Walkley, Carl R.
    GENOME BIOLOGY, 2019, 20 (01)
  • [22] A-to-I RNA editing as a tuner of noncoding RNAs in cancer
    Liao, Yuanfan
    Jung, Seung Ho
    Kim, Taewan
    CANCER LETTERS, 2020, 494 : 88 - 93
  • [23] RNA A-to-I editing, environmental exposure, and human diseases
    Cayir, Akin
    CRITICAL REVIEWS IN TOXICOLOGY, 2021, 51 (05) : 456 - 466
  • [24] A-to-I RNA editing — immune protector and transcriptome diversifier
    Eli Eisenberg
    Erez Y. Levanon
    Nature Reviews Genetics, 2018, 19 : 473 - 490
  • [25] RADAR: a rigorously annotated database of A-to-I RNA editing
    Ramaswami, Gokul
    Li, Jin Billy
    NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) : D109 - D113
  • [26] The majority of A-to-I RNA editing is not required for mammalian homeostasis
    Alistair M. Chalk
    Scott Taylor
    Jacki E. Heraud-Farlow
    Carl R. Walkley
    Genome Biology, 20
  • [27] De Novo A-to-I RNA Editing Discovery in lncRNA
    Silvestris, Domenico Alessandro
    Scopa, Chiara
    Hanchi, Sara
    Locatelli, Franco
    Gallo, Angela
    CANCERS, 2020, 12 (10) : 1 - 13
  • [28] The preponderance of nonsynonymous A-to-I RNA editing in coleoids is nonadaptive
    Jiang, Daohan
    Zhang, Jianzhi
    NATURE COMMUNICATIONS, 2019, 10 (1)
  • [29] A-to-I RNA editing: Recent news and residual mysteries
    Maas, S
    Rich, A
    Nishikura, K
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) : 1391 - 1394
  • [30] A-to-I RNA Editing Contributes to Proteomic Diversity in Cancer
    Peng, Xinxin
    Xu, Xiaoyan
    Wang, Yumeng
    Hawke, David H.
    Yu, Shuangxing
    Han, Leng
    Zhou, Zhicheng
    Mojumdar, Kamalika
    Jeong, Kang Jin
    Labrie, Marilyne
    Tsang, Yiu Huen
    Zhang, Minying
    Lu, Yiling
    Hwu, Patrick
    Scott, Kenneth L.
    Liang, Han
    Mills, Gordon B.
    CANCER CELL, 2018, 33 (05) : 817 - +