Arabidopsis chloroplast quantitative editotype

被引:86
作者
Ruwe, Hannes [1 ]
Castandet, Benoit [2 ]
Schmitz-Linneweber, Christian [1 ]
Stern, David B. [2 ]
机构
[1] Humboldt Univ, Inst Biol, D-10115 Berlin, Germany
[2] Cornell Univ, Boyce Thompson Inst Plant Res, Ithaca, NY 14853 USA
关键词
RNA editing; Chloroplast; RNA-seq; PNPase; Pentatricopeptide repeat; RNA processing; PENTATRICOPEPTIDE REPEAT PROTEIN; EDITING SITES; RNA; PLASTIDS; TRANSCRIPTION; SEQUENCE; DOMAINS; FAMILY; TARGET;
D O I
10.1016/j.febslet.2013.03.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chloroplast C-to-U RNA editing is an essential post-transcriptional process. Here we analyzed RNA editing in Arabidopsis thaliana using strand-specific deep sequencing datasets from the wild-type and a mutant defective in RNA 3' end maturation. We demonstrate that editing at all sites is partial, with an average of 5-6% of RNAs remaining unedited. Furthermore, we identified nine novel sites with a low extent of editing. Of these, three sites are absent from the WT transcriptome because they are removed by 3' end RNA processing, but these regions accumulate, and are edited, in a mutant lacking polynucleotide phosphorylase. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1429 / 1433
页数:5
相关论文
共 33 条
  • [1] RIP1, a member of an Arabidopsis protein family, interacts with the protein RARE1 and broadly affects RNA editing
    Bentolila, Stephane
    Heller, Wade P.
    Sun, Tao
    Babina, Arianne M.
    Friso, Giulia
    van Wijk, Klaas J.
    Hanson, Maureen R.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (22) : E1453 - E1461
  • [2] TISSUE-SPECIFIC AND STAGE-SPECIFIC MODULATION OF RNA EDITING OF THE PSBF AND PSBL TRANSCRIPT FROM SPINACH PLASTIDS - A NEW REGULATORY MECHANISM
    BOCK, R
    HAGEMANN, R
    KOSSEL, H
    KUDLA, J
    [J]. MOLECULAR & GENERAL GENETICS, 1993, 240 (02): : 238 - 244
  • [3] RNA Editing in Plant Organelles. Why Make It Easy?
    Castandet, B.
    Araya, A.
    [J]. BIOCHEMISTRY-MOSCOW, 2011, 76 (08) : 924 - 931
  • [4] Cross-competition in transgenic chloroplasts expressing single editing sites reveals shared cis elements
    Chateigner-Boutin, AL
    Hanson, MR
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (24) : 8448 - 8456
  • [5] A rapid high-throughput method for the detection and quantification of RNA editing based on high-resolution melting of amplicons
    Chateigner-Boutin, Anne-Laure
    Small, Ian
    [J]. NUCLEIC ACIDS RESEARCH, 2007, 35 (17)
  • [6] Plant RNA editing
    Chateigner-Boutin, Anne-Laure
    Small, Ian
    [J]. RNA BIOLOGY, 2010, 7 (02) : 213 - 219
  • [7] PCR amplification introduces errors into mononucleotide and dinucleotide repeat sequences
    Clarke, LA
    Rebelo, CS
    Gonçalves, J
    Boavida, MG
    Jordan, P
    [J]. JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2001, 54 (05): : 351 - 353
  • [8] TRANSCRIPTION OF SINGLE BASE OLIGONUCLEOTIDES BY RIBONUCLEIC ACID-DIRECTED DEOXYRIBONUCLEIC-ACID POLYMERASE
    FALVEY, AK
    WEISS, GB
    KRUEGER, LJ
    KANTOR, JA
    ANDERSON, WF
    [J]. NUCLEIC ACIDS RESEARCH, 1976, 3 (01) : 79 - 88
  • [9] Rapid evolution of RNA editing sites in a small non-essential plastid gene
    Fiebig, A
    Stegemann, S
    Bock, R
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 (12) : 3615 - 3622
  • [10] Mutational analysis of Arabidopsis chloroplast polynucleotide phosphorylase reveals roles for both RNase PH core domains in polyadenylation, RNA 3′-end maturation and intron degradation
    Germain, Arnaud
    Herlich, Shira
    Larom, Shirley
    Kim, Sang Hu
    Schuster, Gadi
    Stern, David B.
    [J]. PLANT JOURNAL, 2011, 67 (03) : 381 - 394