A single alteration 20 nt 5' to an editing target inhibits chloroplast RNA editing in vivo.
about
Expression of complementary RNA from chloroplast transgenes affects editing efficiency of transgene and endogenous chloroplast transcriptsHigh-level expression of a synthetic red-shifted GFP coding region incorporated into transgenic chloroplasts.Loss of matK RNA editing in seed plant chloroplasts.Heterologous, splicing-dependent RNA editing in chloroplasts: allotetraploidy provides trans-factors.Transcript abundance supercedes editing efficiency as a factor in developmental variation of chloroplast gene expressionMaintenance of plastid RNA editing activities independently of their target sites.Eukaryotic genome evolution: rearrangement and coevolution of compartmentalized genetic informationA site-specific factor interacts directly with its cognate RNA editing site in chloroplast transcripts.Conserved domain structure of pentatricopeptide repeat proteins involved in chloroplast RNA editing.Characteristics and prediction of RNA editing sites in transcripts of the Moss Takakia lepidozioides chloroplastAmino acid sequence variations in Nicotiana CRR4 orthologs determine the species-specific efficiency of RNA editing in plastids.Post-transcriptional control of chloroplast gene expression.Recognition of RNA editing sites is directed by unique proteins in chloroplasts: biochemical identification of cis-acting elements and trans-acting factors involved in RNA editing in tobacco and pea chloroplastsCross-competition in transgenic chloroplasts expressing single editing sites reveals shared cis elements.Complex cis-elements determine an RNA editing site in pea mitochondria.Two RNA editing sites with cis-acting elements of moderate sequence identity are recognized by an identical site-recognition protein in tobacco chloroplasts.Cross-competition in editing of chloroplast RNA transcripts in vitro implicates sharing of trans-factors between different C targetsAn in vitro RNA editing system from cauliflower mitochondria: editing site recognition parameters can vary in different plant species.A pentatricopeptide repeat protein acts as a site-specificity factor at multiple RNA editing sites with unrelated cis-acting elements in plastids.Sequence elements critical for efficient RNA editing of a tobacco chloroplast transcript in vivo and in vitro.A comparative genomics approach identifies a PPR-DYW protein that is essential for C-to-U editing of the Arabidopsis chloroplast accD transcript.A study of new Arabidopsis chloroplast RNA editing mutants reveals general features of editing factors and their target sites.RNA editing sites in plant mitochondria can share cis-elements.A simple in vitro RNA editing assay for chloroplast transcripts using fluorescent dideoxynucleotides: distinct types of sequence elements required for editing of ndh transcripts.
P2860
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P2860
A single alteration 20 nt 5' to an editing target inhibits chloroplast RNA editing in vivo.
description
2001 nî lūn-bûn
@nan
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@ast
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@en
type
label
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@ast
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@en
prefLabel
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@ast
A single alteration 20 nt 5' t ...... loroplast RNA editing in vivo.
@en
P2860
P356
P1476
A single alteration 20 nt 5' t ...... hloroplast RNA editing in vivo
@en
P2093
P2860
P304
P356
10.1093/NAR/29.7.1507
P407
P50
P577
2001-04-01T00:00:00Z