In-Depth Bioinformatic Analyses of Nidovirales Including Human SARS-CoV-2, SARS-CoV, MERS-CoV Viruses Suggest Important Roles of Non-canonical Nucleic Acid Structures in Their Lifecycles

被引:51
作者
Bartas, Martin [1 ]
Brazda, Vaclav [2 ,3 ]
Bohalova, Natalia [2 ,4 ]
Cantara, Alessio [2 ,4 ]
Volna, Adriana [5 ]
Stachurova, Tereza [1 ]
Malachova, Katerina [1 ]
Jagelska, Eva B. [2 ]
Porubiakova, Otilia [2 ,3 ]
Cerven, Jiri [1 ]
Pecinka, Petr [1 ]
机构
[1] Univ Ostrava, Fac Sci, Dept Biol & Ecol, Ostrava, Czech Republic
[2] Acad Sci Czech Republ, Inst Biophys, Dept Biophys Chem & Mol Oncol, Brno, Czech Republic
[3] Brno Univ Technol, Fac Chem, Brno, Czech Republic
[4] Masaryk Univ, Fac Sci, Dept Expt Biol, Brno, Czech Republic
[5] Univ Ostrava, Fac Sci, Dept Phys, Ostrava, Czech Republic
关键词
coronavirus; genome; RNA; G-quadruplex; inverted repeats; G-QUADRUPLEX STRUCTURES; WEB-BASED SERVER; MOLECULAR-BIOLOGY; RNA; DNA; CORONAVIRUS; PROTEIN; GENOME; TARGETS; ORGANIZATION;
D O I
10.3389/fmicb.2020.01583
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Non-canonical nucleic acid structures play important roles in the regulation of molecular processes. Considering the importance of the ongoing coronavirus crisis, we decided to evaluate genomes of all coronaviruses sequenced to date (stated more broadly, the orderNidovirales) to determine if they contain non-canonical nucleic acid structures. We discovered much evidence of putative G-quadruplex sites and even much more of inverted repeats (IRs) loci, which in fact are ubiquitous along the whole genomic sequence and indicate a possible mechanism for genomic RNA packaging. The most notable enrichment of IRs was found inside 5 ' UTR for IRs of size 12+ nucleotides, and the most notable enrichment of putative quadruplex sites (PQSs) was located before 3 ' UTR, inside 5 ' UTR, and before mRNA. This indicates crucial regulatory roles for both IRs and PQSs. Moreover, we found multiple G-quadruplex binding motifs in human proteins having potential for binding of SARS-CoV-2 RNA. Non-canonical nucleic acids structures inNidoviralesand in novel SARS-CoV-2 are therefore promising druggable structures that can be targeted and utilized in the future.
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页数:16
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