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onsdag 27 maj 2020

Influenssa ja mikroRNA-kirjo . Käsitys RNA virus ten kyvystä miRNA muodsotukseen

. 2016 Nov; 26(6): 389–407.
Published online 2016 Jul 4. doi: 10.1002/rmv.1894
PMCID: PMC7169129
PMID: 27373545

The role of microRNAs in respiratory viral infection: friend or foe?

Abbreviations

microRNAs
miRNAs
nucleotide
nt
precursor miRNAs
pre‐miRNA
RNA‐induced silencing complex
RISC
three prime untranslated region
3ʹ‐UTR
nuclear factor kappa B
NF‐kB
interleukin‐1 receptor‐associated kinase
IRAK
chemokine (C‐C motif) ligand
CCL
nerve growth factor
NGF
tropomyosin‐related kinase A
TrkA
severe acute respiratory syndrome‐coronavirus
SARS‐CoV
Middle East respiratory syndrome‐coronavirus
MERS‐CoV
OC43‐coronavirus
OC43‐CoV
very low‐density lipoprotein receptor
VLDLR
human metapneumovirus
HMPV
virus‐associated RNAs
VARNAs
 Figure 1
Following viral infection, host cells alter their microRNAs (miRNAs) expression as a defense against infection, while viruses can circumvent host defense and promote their own propagation by affecting host cellular miRNAs expression or by expressing their own miRNAs

miRNAs, microRNAs; TGF‐β, transforming growth factor‐β; COX6C, cytochrome c oxidase VIC; NGF, nerve growth factor; TrkA, tropomyosin‐related kinase A; NF‐kB, nuclear factor kappa B; HMPV, human metapneumovirus; HCMV, human cytomegalovirus; CAR, Coxsackie virus and adenovirus receptor; HDGF, hepatoma‐derived growth factor.

(Uppfattning,  Käsitys 2016) :
"RNA Viruses


Unlike DNA viruses, RNA viruses usually do not encode their own miRNA, and the reasons behind this discrepancy are debated theoretically 89. The majority of RNA viruses replicate in the cytoplasm where they cannot access the nuclear enzyme Drosha, which is required for miRNA processing. Those RNA viruses, which do have access to the nucleus (e.g. influenza and HIV‐1), may avoid encoding their own miRNAs because excision of a primary miRNA from RNA virus genome would induce cleavage and destruction of viral genome 20, 27. In addition, viruses that undergo short lytic replication cycles are less likely to encode miRNAs 22."


Influenza infection of airway epithelial cells induces or inhibits certain cellular microRNAs (miRNAs) expression in favor of viral replication, pathogenesis, and also suppress anti‐viral responses. However, certain cellular miRNAs can inhibit replication of influenza in infected cells, and certain miRNAs play important roles in priming airway cells for repair and regeneration following influenza infection



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