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tRNA modifications in viral replication
DOI:10.1016/j.jbc.2026.111430.png)
摘要
En 中文
tRNA修饰是在外部和细胞应激条件下对转录后基因表达调控的关键因素。病毒感染是一种常见的外部应激,它会劫持细胞过程以进行复制。宿主细胞的tRNA池和修饰谱在病毒感染期间通常会被重塑,从而引发促病毒和抗病毒效应。宿主tRNA修饰的变化,特别是在反密码子序列中的变化,有能力重编程宿主和病毒的蛋白质组。例如,反密码环修饰有助于产生某些病毒蛋白所必需的程序性核糖体移码。然而,tRNA修饰在病毒感染中的作用并不仅限于翻译过程。反转录病毒使用选择的宿主细胞tRNA作为反转录引物,而修饰则调节反转录过程中的各个步骤。此外,一些非引物修饰的tRNA被选择性地包装到病毒颗粒中,尽管其功能尚不清楚。病毒编码的tRNA含有修饰,以扩展反密码子池,因为宿主tRNA被耗尽。在病毒感染后,多种tRNA修饰酶的表达和活性受到调控,其功能意义有待阐明。tRNA修饰参与抗病毒防御,特别是在病毒感染后,反密码环处的tRNA裂解会导致产生tRNA衍生片段。尽管大多数病毒感染后tRNA修饰景观很可能发生显著改变,但目前的证据仅限于少数特定实例。在病毒感染期间进行全局tRNA组分析将阐明这些及其他过程的调控机制。新兴技术,包括直接tRNA测序的进步以及通过质谱检测修饰的方法,正在使这一目标成为可能。
Keyword:
transfer RNA (tRNA)
RNA modification
viral replication
translation regulation
reverse transcription
codon usage
anti-viral immune response
tRNA-modifying enzymes
tRNA-derived RNA (tDR)
tRNA-like structures (TLS)
AC
anticodon
D
dihydrouridine
PRF
programmed ribosomal frameshifting
TLS
tRNA-like structures
DENV
dengue virus
CHIKV
chikungunya virus
HTLV-1
human T-lymphotropic virus-1
SARS-CoV-2
severe acute respiratory syndrome coronavirus-2
RSV
respiratory syncytial virus
HEV
Hepatitis E virus
SLFN
Schlafen
t6A
N6-threonylcarbamoyladenosine
ms2t6A,methylthio-t6A
m1A
1-methyladenosine
HCMV
human cytomegalovirus
yW
wybutosine
m3C
3-methylcytidine
TRMT61A and TRMT6
tRNA methyltransferase 61A and 6
mcm5U
5-methoxycarbonylmethyluridine
mcm5s2U
5-methoxycarbonylmethyl-2-thiouridine
mchm5U
5-methoxy-carbonyl-hydroxy-methyluridine
ALKBH8
ALKB homolog 8
f5C
5-formylcytidine
f5Cm
5-formyl-2'-O-methylcytidine
Elp1
elongator complex protein 1
I
inosine
i6A
isopentenyl adenosine
Q
queuosine
MCP
major capsid protein
MMTV
mouse mammary tumor virus
BLV
bovine leukemia virus
m1G
1-methylguanosine
s2U34
2-thiouridine
ncRNAs
non-coding RNAs
snRNA
spliceosomal U6 small nuclear RNA
SRP
signal recognition particle
LysRS
lysyl-tRNA synthetase
NTD
N-terminal domain
m2G
N2-methylguanosine
TLRs
toll-like receptors
CA
capsid
m5C
5-methylcytidine
m6A
N6-methyladenosine
m5U
5-methyluridine
ψ
pseudouridine
m1Gm
1,2'-O-dimethylguanosine
m5Um
5,2'-O-dimethyluridine
LC/MS
liquid chromatography-mass spectrometry
Am
2′-O-methyladenosine
m6t6A
N6-methyl-N6-threonylcarbamoyladenosine
Cm, 2'-O-methylcytidine
NC
nucleocapsid
RT
Reverse transcriptase
PBS
primer binding site
PAS
primer activation signal
ASLV
avian sarcoma and leukosis virus
M-MuLV
Moloney murine leukemia virus
PPT
poly-purine tract
+sss
plus-strand strong-stop
TRMT1
tRNA methyltransferase 1
m2,2G
N2,N2-dimethylguanosine
MPro/Nsp5
main protease/non-structural protein 5
HCV
Hepatitis C virus
ANG
angiogenin
s4U
4-thiouridine
acp3U
3-(3-amino-3-carboxypropyl)uridine
k2C
2-lysidine
cmnm5s2U
5-carboxymethylaminomethyl-2-thiouridine
TMV
tobacco mosaic virus
TYMV
turnip yellow mosaic virus
ACNases
Anticodon nucleases
mnm5s2U34
5-methylaminomethyl-2-thiouridine
VLE
virus-like elements
SAMD9
sterile alpha motif domain-containing 9
2-5A
2′-5′-linked oligoadenylates
IFNs
type-I interferons
ONT
Oxford nanopore technology
Im
2'-O-methylinosine
m1I
1-methylinosine
m2A
2-methyladenosine
mnm5U
5-methylaminomethyluridine
ncm5U
5-carbamoylmethyluridine
m6Am
N6,2'-O-dimethyladenosine
mim-tRNAseq
modification-induced misincorporation tRNA sequencing
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期刊
IF:
3.9
论文数:
11.2W
被引数:
28.3W
机构
引用论文
Improvement of reading frame maintenance is a common function for several tRNA modifications
EMBO JOURNAL
IF8.3
Codon usage bias from tRNA's point of view: Redundancy, specialization, and efficient decoding for translation optimization
GENOME RESEARCH
IF5.5
Quantitative analysis of tRNA abundance and modifications by nanopore RNA sequencing通过纳米孔RNA测序定量分析tRNA丰度和修饰
NATURE BIOTECHNOLOGY
IF41.7
Connecting tRNA Charging and Decoding through the Axis of Nucleotide Modifications at Position 37通过第37位核苷酸修饰轴连接tRNA的氨基酸负载和密码子识别
Decreasing the frameshift efficiency translates into an equivalent reduction of the replication of the human immunodeficiency virus type 1
Virology
IF0

