Unravelling tRNA fragments in DENV pathogenesis: Insights from RNA sequencing

被引:4
作者
Madhry, Deeksha [1 ]
Kumari, Kiran [1 ]
Meena, Varsha [1 ]
Roy, Riya [1 ]
Verma, Bhupendra [1 ]
机构
[1] All India Inst Med Sci, Dept Biotechnol, New Delhi 110029, India
关键词
DENV; Host-virus interaction; Non-coding RNA; tRNA-derived RNA fragment; Small RNA sequencing; RNases; IDENTIFICATION; ANGIOGENIN; CANCER; BREAST;
D O I
10.1038/s41598-024-69391-7
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
Small non-coding RNAs (sncRNAs) derived from tRNAs are known as tRNA-derived small RNAs (tsRNAs). These tsRNAs are further categorized into tRNA-derived fragments (tRFs) and tRNA halves (tiRNAs), which play significant roles in the various molecular mechanisms underlying certain human diseases. However, the generation of tsRNAs and their potential roles during Dengue virus (DENV) infection is not yet known. Here, we performed small RNA sequencing to identify the generation and alterations in tsRNAs expression profiles of DENV-infected Huh7 cells. Upon DENV infection, tRNA fragmentation was found to be increased. We identified a significant number of differentially expressed tsRNAs during DENV infection. Interestingly, the 3 ' tRF population showed upregulation, while the i-tRF population exhibited downregulation. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was performed to analyze the impact of differentially expressed tsRNAs on DENV pathogenesis. Our results suggest that differentially expressed tsRNAs are involved in transcriptional regulation via RNA polymerase II promoter and metabolic pathways. Overall, our study contributes significantly to our understanding of the roles played by tsRNAs in the complex dynamics of DENV infection.
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页数:10
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共 50 条
[1]   tRNA fragments in human health and disease [J].
Anderson, Paul ;
Ivanov, Pavel .
FEBS LETTERS, 2014, 588 (23) :4297-4304
[2]   G3BP1, G3BP2 and CAPRIN1 Are Required for Translation of Interferon Stimulated mRNAs and Are Targeted by a Dengue Virus Non-coding RNA [J].
Bidet, Katell ;
Dadlani, Dhivya ;
Garcia-Blanco, Mariano A. .
PLOS PATHOGENS, 2014, 10 (07)
[3]   Complex Modulation of the Aedes aegypti Transcriptome in Response to Dengue Virus Infection [J].
Bonizzoni, Mariangela ;
Dunn, W. Augustine ;
Campbell, Corey L. ;
Olson, Ken E. ;
Marinotti, Osvaldo ;
James, Anthony A. .
PLOS ONE, 2012, 7 (11)
[4]   Cyclin-Dependent Kinases 8 and 19 Regulate Host Cell Metabolism during Dengue Virus Serotype 2 Infection [J].
Butler, Molly ;
Chotiwan, Nunya ;
Brewster, Connie D. ;
DiLisio, James E. ;
Ackart, David F. ;
Podell, Brendan K. ;
Basaraba, Randall J. ;
Perera, Rushika ;
Quackenbush, Sandra L. ;
Rovnak, Joel .
VIRUSES-BASEL, 2020, 12 (06)
[5]  
Cristodero M, 2017, Non-coding RNA Investigation, V1, P7, DOI [10.21037/ncri.2017.08.07, 10.21037/ncri.2017.08.07, DOI 10.21037/NCRI.2017.08.07]
[6]   Functional Interplay between RNA Viruses and Non-Coding RNA in Mammals [J].
Damas, Nkerorema Djodji ;
Fossat, Nicolas ;
Scheel, Troels K. H. .
NON-CODING RNA, 2019, 5 (01)
[7]   Respiratory Syncytial Virus Utilizes a tRNA Fragment to Suppress Antiviral Responses Through a Novel Targeting Mechanism [J].
Deng, Junfang ;
Ptashkin, Ryan N. ;
Chen, Yu ;
Cheng, Zhi ;
Liu, Guangliang ;
Phan, Thien ;
Deng, Xiaoling ;
Zhou, Jiehua ;
Lee, Inhan ;
Lee, Yong Sun ;
Bao, Xiaoyong .
MOLECULAR THERAPY, 2015, 23 (10) :1622-1629
[8]   Non-coding RNA genes and the modern RNA world [J].
Eddy, SR .
NATURE REVIEWS GENETICS, 2001, 2 (12) :919-929
[9]   tiRNAs as a novel biomarker for cell damage assessment in in vitro ischemia-reperfusion model in rat neuronal PC12 cells [J].
Elkordy, Alaa ;
Rashad, Sherif ;
Shehabeldeen, Heba ;
Mishima, Eikan ;
Niizuma, Kuniyasu ;
Abe, Takaaki ;
Tominaga, Teiji .
BRAIN RESEARCH, 2019, 1714 :8-17
[10]   Stress-induced tRNA cleavage and tiRNA generation in rat neuronal PC12 cells [J].
Elkordy, Alaa ;
Mishima, Eikan ;
Niizuma, Kuniyasu ;
Akiyama, Yasutoshi ;
Fujimura, Miki ;
Tominaga, Teiji ;
Abe, Takaaki .
JOURNAL OF NEUROCHEMISTRY, 2018, 146 (05) :560-569