Home LiteratureArticle Details
PMID: 10688364 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

A phylogenetic analysis reveals an unusual sequence conservation within introns involved in RNA editing.

RNA (New York, N.Y.) ·Vol. 6 ·No. 2 ·2000-02-00 ·Pages 257-69

Aruscavage PJ, Bass BL

Abstract

Adenosine deaminases that act on RNA (ADARs) are RNA editing enzymes that convert adenosines to inosines within cellular and viral RNAs. Certain glutamate receptor (gluR) pre-mRNAs are substrates for the enzymes in vivo. For example, at the R/G editing site of gluR-B, -C, and -D RNAs, ADARs change an arginine codon (AGA) to a glycine codon (IGA) so that two protein isoforms can be synthesized from a single encoded mRNA; the highly related gluR-A sequence is not edited at this site. To gain insight into what features of an RNA substrate are important for accurate and efficient editing by an ADAR, we performed a phylogenetic analysis of sequences required for editing at the R/G site. We observed highly conserved sequences that were shared by gluR-B, -C, and -D, but absent from gluR-A. Surprisingly, in contrast to results obtained in phylogenetic analyses of tRNA and rRNA, it was the bases in paired, helical regions whose identity was conserved, whereas bases in nonhelical regions varied, but maintained their nonhelical state. We speculate this pattern in part reflects constraints imposed by ADAR's unique specificity and gained support for our hypotheses with mutagenesis studies. Unexpectedly, we observed that some of the gluR introns were conserved beyond the sequences required for editing. The approximately 600-nt intron 13 of gluR-C was particularly remarkable, showing >94% nucleotide identity between human and chicken, organisms estimated to have diverged 310 million years ago.

MeSH Terms
Adenosine Deaminase/metabolism Animals Base Sequence Conserved Sequence DNA Primers/genetics DNA, Complementary/genetics Humans Introns Molecular Sequence Data Mutagenesis Nucleic Acid Conformation Phylogeny RNA Editing/genetics RNA Precursors/chemistry,genetics,metabolism RNA-Binding Proteins Receptors, Glutamate/genetics Sequence Homology, Nucleic Acid Species Specificity Substrate Specificity
Chemicals
DNA Primers DNA, Complementary RNA Precursors RNA-Binding Proteins Receptors, Glutamate ADARB1 protein, human Adenosine Deaminase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Aruscavage P J
Department of Biochemistry/Howard Hughes Medical Institute, University of Utah, Salt Lake City 84132, USA.
Bass B L
References (28)
28 references, click to expand
  1. Lessons from an evolving rRNA: 16S and 23S rRNA structures from a comparative perspective.
    Microbiol Rev. 1994 Mar;58(1):10-26 PMID: 8177168
  2. The importance of internal loops within RNA substrates of ADAR1.
    J Mol Biol. 1999 Aug 6;291(1):1-13 PMID: 10438602
  3. Preferential selection of adenosines for modification by double-stranded RNA adenosine deaminase.
    EMBO J. 1994 Dec 1;13(23):5701-11 PMID: 7527340
  4. Control of kinetic properties of AMPA receptor channels by nuclear RNA editing.
    Science. 1994 Dec 9;266(5191):1709-13 PMID: 7992055
  5. Human and rodent DNA sequence comparisons: a mosaic model of genomic evolution.
    Trends Genet. 1995 Sep;11(9):367-71 PMID: 7482789
  6. Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice.
    Science. 1995 Dec 8;270(5242):1677-80 PMID: 7502080
  7. RNA editing of hepatitis delta virus antigenome by dsRNA-adenosine deaminase.
    Nature. 1996 Apr 4;380(6573):454-6 PMID: 8602246
  8. CDNA cloning of chick brain alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors reveals conservation of structure, function and post-transcriptional processes with mammalian receptors.
    Brain Res Mol Brain Res. 1996 Feb;36(1):101-13 PMID: 9011745
  9. Purification and characterization of a human RNA adenosine deaminase for glutamate receptor B pre-mRNA editing.
    Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4354-9 PMID: 9113993
  10. Regulation of serotonin-2C receptor G-protein coupling by RNA editing.
    Nature. 1997 May 15;387(6630):303-8 PMID: 9153397
  11. RNA editing and hypermutation by adenosine deamination.
    Trends Biochem Sci. 1997 May;22(5):157-62 PMID: 9175473
  12. RNA editing: rewriting receptors.
    Curr Biol. 1997 Jul 1;7(7):R437-9 PMID: 9210370
  13. A standardized nomenclature for adenosine deaminases that act on RNA.
    RNA. 1997 Sep;3(9):947-9 PMID: 9292492
  14. Long human-mouse sequence alignments reveal novel regulatory elements: a reason to sequence the mouse genome.
    Genome Res. 1997 Oct;7(10):959-66 PMID: 9331366
  15. Inosine exists in mRNA at tissue-specific levels and is most abundant in brain mRNA.
    EMBO J. 1998 Feb 16;17(4):1120-7 PMID: 9463389
  16. Sequence-specific recognition of double helical nucleic acids by proteins.
    Proc Natl Acad Sci U S A. 1976 Mar;73(3):804-8 PMID: 1062791
  17. Transfer RNA: molecular structure, sequence, and properties.
    Annu Rev Biochem. 1976;45:805-60 PMID: 60910
  18. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences.
    J Mol Evol. 1980 Dec;16(2):111-20 PMID: 7463489
  19. Secondary structure of 16S ribosomal RNA.
    Science. 1981 Apr 24;212(4493):403-11 PMID: 6163215
  20. Evolution of large-subunit rRNA structure. The diversification of divergent D3 domain among major phylogenetic groups.
    Eur J Biochem. 1990 Mar 10;188(2):219-29 PMID: 2138538
  21. Flip and flop: a cell-specific functional switch in glutamate-operated channels of the CNS.
    Science. 1990 Sep 28;249(4976):1580-5 PMID: 1699275
  22. Ca2+ permeability of unedited and edited versions of the kainate selective glutamate receptor GluR6.
    Proc Natl Acad Sci U S A. 1993 Jan 15;90(2):755-9 PMID: 7678465
  23. RNA editing of AMPA receptor subunit GluR-B: a base-paired intron-exon structure determines position and efficiency.
    Cell. 1993 Dec 31;75(7):1361-70 PMID: 8269514
  24. Purification of the Xenopus laevis double-stranded RNA adenosine deaminase.
    J Biol Chem. 1994 Apr 1;269(13):9933-9 PMID: 8144588
  25. A molecular timescale for vertebrate evolution.
    Nature. 1998 Apr 30;392(6679):917-20 PMID: 9582070
  26. RNA editing of brain glutamate receptor channels: mechanism and physiology.
    Brain Res Brain Res Rev. 1998 May;26(2-3):217-29 PMID: 9651532
  27. Molecular analysis of AMPA-specific receptors: subunit composition, editing, and calcium influx determination in small amounts of tissue.
    Brain Res Brain Res Protoc. 1998 Nov;3(2):142-54 PMID: 9813290
  28. Cloned glutamate receptors.
    Annu Rev Neurosci. 1994;17:31-108 PMID: 8210177
Article Info
Journal
RNA (New York, N.Y.)
Abbr.
RNA
ISSN
1355-8382
Published
2000-02-00
Pages
257-69
Language
English
Region
United States
NLM ID
9509184
PMCID
PMC1369911
Subset
IM
Grants
NIGMS NIH HHS · R01 GM044073 · United States
NIGMS NIH HHS · R01 GM044073-11 · United States
NCI NIH HHS · 5P30CA42014 · United States
NIGMS NIH HHS · GM44073 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com