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 chloroplasts
about
Genome-wide analysis of Arabidopsis pentatricopeptide repeat proteins reveals their essential role in organelle biogenesisReverse genetic screening identifies five E-class PPR proteins involved in RNA editing in mitochondria of Arabidopsis thalianaExpression of complementary RNA from chloroplast transgenes affects editing efficiency of transgene and endogenous chloroplast transcriptsComprehensive High-Resolution Analysis of the Role of an Arabidopsis Gene Family in RNA EditingAn RNA recognition motif-containing protein is required for plastid RNA editing in Arabidopsis and maize.Complete chloroplast genome sequence of Magnolia kwangsiensis (Magnoliaceae): implication for DNA barcoding and population genetics.Transcriptomic analysis of salt stress responsive genes in Rhazya stricta.The E-class PPR protein MEF3 of Arabidopsis thaliana can also function in mitochondrial RNA editing with an additional DYW domain.Molecular evolution of pentatricopeptide repeat genes reveals truncation in species lacking an editing target and structural domains under distinct selective pressuresNMR structure of the apoB mRNA stem-loop and its interaction with the C to U editing APOBEC1 complementary factor.MEF10 is required for RNA editing at nad2-842 in mitochondria of Arabidopsis thaliana and interacts with MORF8.Maintenance of plastid RNA editing activities independently of their target sites.The pentatricopeptide repeat protein OTP87 is essential for RNA editing of nad7 and atp1 transcripts in Arabidopsis mitochondriaA site-specific factor interacts directly with its cognate RNA editing site in chloroplast transcripts.Frequent chloroplast RNA editing in early-branching flowering plants: pilot studies on angiosperm-wide coexistence of editing sites and their nuclear specificity factorsGenetic architecture of mitochondrial editing in Arabidopsis thaliana.Amino acid sequence variations in Nicotiana CRR4 orthologs determine the species-specific efficiency of RNA editing in plastids.Post-transcriptional control of chloroplast gene expression.Different patterns in the recognition of editing sites in plant mitochondria.When you can't trust the DNA: RNA editing changes transcript sequences.RNA editing in hornwort chloroplasts makes more than half the genes functional.Developmental co-variation of RNA editing extent of plastid editing sites exhibiting similar cis-elements.Complex cis-elements determine an RNA editing site in pea mitochondria.Multiple specificity recognition motifs enhance plant mitochondrial RNA editing in vitro.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.Identification of a sequence motif critical for editing of a tobacco chloroplast transcript.A pentatricopeptide repeat protein acts as a site-specificity factor at multiple RNA editing sites with unrelated cis-acting elements in plastids.Organellar RNA editing and plant-specific extensions of pentatricopeptide repeat proteins in jungermanniid but not in marchantiid liverworts.The SLO1 PPR protein is required for RNA editing at multiple sites with similar upstream sequences in Arabidopsis mitochondria.The longest mitochondrial RNA editing PPR protein MEF12 in Arabidopsis thaliana requires the full-length E domain.Faithful editing of a tomato-specific mRNA editing site in transgenic tobacco chloroplasts.Sequence elements critical for efficient RNA editing of a tobacco chloroplast transcript in vivo and in vitro.Identification of the chloroplast adenosine-to-inosine tRNA editing enzyme.A study of new Arabidopsis chloroplast RNA editing mutants reveals general features of editing factors and their target sites.Two interacting proteins are necessary for the editing of the NdhD-1 site in Arabidopsis plastids.In vitro RNA editing in pea mitochondria requires NTP or dNTP, suggesting involvement of an RNA helicase.Quantitative analysis of motifs contributing to the interaction between PLS-subfamily members and their target RNA sequences in plastid RNA editing.The DYW-E-PPR protein MEF14 is required for RNA editing at site matR-1895 in mitochondria of Arabidopsis thaliana.
P2860
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P2860
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 chloroplasts
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Recognition of RNA editing sit ...... n tobacco and pea chloroplasts
@en
Recognition of RNA editing sit ...... tobacco and pea chloroplasts.
@nl
type
label
Recognition of RNA editing sit ...... n tobacco and pea chloroplasts
@en
Recognition of RNA editing sit ...... tobacco and pea chloroplasts.
@nl
prefLabel
Recognition of RNA editing sit ...... n tobacco and pea chloroplasts
@en
Recognition of RNA editing sit ...... tobacco and pea chloroplasts.
@nl
P2093
P2860
P1476
Recognition of RNA editing sit ...... n tobacco and pea chloroplasts
@en
P2093
Junichi Obokata
Masahiro Sugiura
Tetsuya Miyamoto
P2860
P304
P356
10.1128/MCB.22.19.6726-6734.2002
P407
P577
2002-10-01T00:00:00Z