A small interfering RNA (siRNA) database for SARS-CoV-2

被引:18
作者
Medeiros, Inacio Gomes [1 ,3 ]
Khayat, Andre Salim [5 ]
Stransky, Beatriz [2 ,4 ]
Santos, Sidney [5 ]
Assumpcao, Paulo [6 ]
Santana de Souza, Jorge Estefano [1 ,2 ]
机构
[1] Univ Fed Rio Grande do Norte, Metropole Digital Inst, Bioinformat Grad Program, BR-59078400 Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, Metropole Digital Inst, Bioinformat Multidisciplinary Environm BioME, BR-59078400 Natal, RN, Brazil
[3] Univ Fed Rio Grande do Norte, Inst Cerebro, BR-59078970 Natal, RN, Brazil
[4] Univ Fed Rio Grande do Norte, Ctr Technol, Biomed Engn Dept, BR-59078970 Natal, RN, Brazil
[5] Univ Fed Para, Inst Ciencias Biol, BR-66075110 Belem, Para, Brazil
[6] Univ Fed Para, Nucleo Pesquisas Oncol, BR-66073110 Belem, Para, Brazil
关键词
SARS CORONAVIRUS; IN-VITRO; THERAPEUTICS; DELIVERY; INHIBITION; EXPRESSION; SEQUENCES; RESPONSES; ANTISENSE; DESIGN;
D O I
10.1038/s41598-021-88310-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Coronavirus disease 2019 (COVID-19) rapidly transformed into a global pandemic, for which a demand for developing antivirals capable of targeting the SARS-CoV-2 RNA genome and blocking the activity of its genes has emerged. In this work, we presented a database of SARS-CoV-2 targets for small interference RNA (siRNA) based approaches, aiming to speed the design process by providing a broad set of possible targets and siRNA sequences. The siRNAs sequences are characterized and evaluated by more than 170 features, including thermodynamic information, base context, target genes and alignment information of sequences against the human genome, and diverse SARS-CoV-2 strains, to assess possible bindings to off-target sequences. This dataset is available as a set of four tables, available in a spreadsheet and CSV (Comma-Separated Values) formats, each one corresponding to sequences of 18, 19, 20, and 21 nucleotides length, aiming to meet the diversity of technology and expertise among laboratories around the world. A metadata table (Supplementary Table S1), which describes each feature, is also provided in the aforementioned formats. We hope that this database helps to speed up the development of new target antivirals for SARS-CoV-2, contributing to a possible strategy for a faster and effective response to the COVID-19 pandemic.
引用
收藏
页数:10
相关论文
共 67 条
[1]   siRNA and RNAi optimization [J].
Alagia, Adele ;
Eritja, Ramon .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2016, 7 (03) :316-329
[2]  
Ambike S., Research Square, V2020, DOI DOI 10.21203/RS.3.RS-105129/V2
[3]  
[Anonymous], 2020, Coronavirus disease, P198
[4]  
[Anonymous], 2021, TECHNOTE 2 WAYS REDU
[5]   Genetic variation in SARS-CoV-2 may explain variable severity of COVID-19 [J].
Biswas, Subrata K. ;
Mudi, Sonchita R. .
MEDICAL HYPOTHESES, 2020, 143
[6]  
Carneiro J, 2020, bioRxiv, DOI [10.1101/2020.04.19.048991, 10.1101/2020.04.19.048991, DOI 10.1101/2020.04.19.048991]
[7]   SARS, MERS and SARS-CoV-2 (COVID-19) treatment: a patent review [J].
Carvalho Nascimento Junior, Jose Adao ;
Santos, Anamaria Mendonca ;
Quintans-Junior, Lucindo Jose ;
Bandero Walker, Cristiani Isabel ;
Borges, Lysandro Pinto ;
Serafini, Mairim Russo .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2020, 30 (08) :567-579
[8]   Computational Identification of Small Interfering RNA Targets in SARS-CoV-2 [J].
Chen, Wei ;
Feng, Pengmian ;
Liu, Kewei ;
Wu, Meng ;
Lin, Hao .
VIROLOGICA SINICA, 2020, 35 (03) :359-361
[9]   ALARMING COVID VARIANTS SHOW KEY ROLE OF GENOMIC SURVEILLANCE [J].
Cyranoski, David .
NATURE, 2021, 589 (7842) :337-338
[10]  
de Carli GJ, 2020, GENET MOL BIOL, V43, DOI [10.1590/1678-4685-GMB-2019-0300, 10.1590/1678-4685-gmb-2019-0300]