Identification of a sequence within U5 required for human immunodeficiency virus type 1 to stably maintain a primer binding site complementary to tRNA(Met).
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Preferences for the selection of unique tRNA primers revealed from analysis of HIV-1 replication in peripheral blood mononuclear cellsThe structure of the human tRNALys3 anticodon bound to the HIV genome is stabilized by modified nucleosides and adjacent mismatch base pairsPrimer tRNAs for reverse transcriptionThe nucleocapsid protein specifically anneals tRNALys-3 onto a noncomplementary primer binding site within the HIV-1 RNA genome in vitro.Changes in Rous sarcoma virus RNA secondary structure near the primer binding site upon tRNATrp primer annealing.Structural basis for the specificity of the initiation of HIV-1 reverse transcription.A succession of mechanisms stimulate efficient reconstituted HIV-1 minus strand strong stop DNA transferInitiation of HIV-2 reverse transcription: a secondary structure model of the RNA-tRNA(Lys3) duplex.Structural and functional properties of the HIV-1 RNA-tRNA(Lys)3 primer complex annealed by the nucleocapsid protein: comparison with the heat-annealed complexThe primer binding site on the RNA genome of human and simian immunodeficiency viruses is flanked by an upstream hairpin structure.Mutational analysis of the tRNA3Lys/HIV-1 RNA (primer/template) complex.The Interaction between tRNA(Lys) 3 and the primer activation signal deciphered by NMR spectroscopy.tRNA isoacceptor preference prior to retrovirus Gag-Pol junction links primer selection and viral translation.The importance of the A-rich loop in human immunodeficiency virus type 1 reverse transcription and infectivity.Identification of sequences downstream of the primer binding site that are important for efficient replication of human immunodeficiency virus type 1.Nucleotide substitutions within U5 are critical for efficient reverse transcription of human immunodeficiency virus type 1 with a primer binding site complementary to tRNA(His)Multiple biological roles associated with the Rous sarcoma virus 5' untranslated RNA U5-IR stem and loop.Prospects for antisense peptide nucleic acid (PNA) therapies for HIVDestabilization of tRNA3(Lys) from the primer-binding site of HIV-1 genome by anti-A loop polyamide nucleotide analogHuman immunodeficiency virus type-1 reverse transcription can be inhibited in vitro by oligonucleotides that target both natural and synthetic tRNA primers.A structured RNA motif is involved in correct placement of the tRNA(3)(Lys) primer onto the human immunodeficiency virus genome.Does the HIV-1 primer activation signal interact with tRNA3(Lys) during the initiation of reverse transcription?HIV-1 designed to use different tRNAGln isoacceptors prefers to select tRNAThr for replication.Initiation of HIV Reverse TranscriptionGenetic analysis of a unique human immunodeficiency virus type 1 (HIV-1) with a primer binding site complementary to tRNAMet supports a role for U5-PBS stem-loop RNA structures in initiation of HIV-1 reverse transcriptionSequence requirements for removal of tRNA by an isolated human immunodeficiency virus type 1 RNase H domainPreferential completion of human immunodeficiency virus type 1 proviruses initiated with tRNA3Lys rather than tRNA1,2Lys.RNase H requirements for the second strand transfer reaction of human immunodeficiency virus type 1 reverse transcription.Transfer of primer binding site-mutated simian immunodeficiency virus vectors by genetically engineered artificial and hybrid tRNA-like primers.Essential regions of the tRNA primer required for HIV-1 infectivityAnti-TAR polyamide nucleotide analog conjugated with a membrane-permeating peptide inhibits human immunodeficiency virus type 1 production.Selection of retroviral reverse transcription primer is coordinated with tRNA biogenesis.Probing the importance of tRNA anticodon: human immunodeficiency virus type 1 (HIV-1) RNA genome complementarity with an HIV-1 that selects tRNA(Glu) for replication.A mutation in integrase can compensate for mutations in the simian immunodeficiency virus att site.Structure-function relationships of the initiation complex of HIV-1 reverse transcription: the case of mutant viruses using tRNA(His) as primerForced selection of a human immunodeficiency virus type 1 variant that uses a non-self tRNA primer for reverse transcription: involvement of viral RNA sequences and the reverse transcriptase enzyme.Nucleotides within the anticodon stem are important for optimal use of tRNA(Lys,3) as the primer for HIV-1 reverse transcription.Analysis of the replication of HIV-1 forced to use tRNAMet(i) supports a link between primer selection, translation and encapsidation.Impact of forced selection of tRNAs on HIV-1 replication and genome stability highlight preferences for selection of certain tRNAs.Switching the in vitro tRNA usage of HIV-1 by simultaneous adaptation of the PBS and PAS.
P2860
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P2860
Identification of a sequence within U5 required for human immunodeficiency virus type 1 to stably maintain a primer binding site complementary to tRNA(Met).
description
1997 nî lūn-bûn
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1997年の論文
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1997年学术文章
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1997年学术文章
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Identification of a sequence w ...... ing site complementary to tRNA
@nl
Identification of a sequence w ...... te complementary to tRNA(Met).
@en
type
label
Identification of a sequence w ...... ing site complementary to tRNA
@nl
Identification of a sequence w ...... te complementary to tRNA(Met).
@en
prefLabel
Identification of a sequence w ...... ing site complementary to tRNA
@nl
Identification of a sequence w ...... te complementary to tRNA(Met).
@en
P2093
P2860
P1433
P1476
Identification of a sequence w ...... ite complementary to tRNA(Met)
@en
P2093
P2860
P304
P407
P577
1997-01-01T00:00:00Z