Affiliation:
1. Department of Molecular and Cell Biology, The University of Texas at Dallas, Richardson, Texas 75080
Abstract
ABSTRACT
tRNAs encoded on the mitochondrial DNA of
Physarum polycephalum
and
Didymium nigripes
require insertional editing for their maturation. Editing consists of the specific insertion of a single cytidine or uridine relative to the mitochondrial DNA sequence encoding the tRNA. Editing sites are at 14 different locations in nine tRNAs. Cytidine insertion sites can be located in any of the four stems of the tRNA cloverleaf and usually create a G · C base pair. Uridine insertions have been identified in the T loop of tRNA
Lys
from
Didymium
and tRNA
Glu
from
Physarum
. In both tRNAs, the insertion creates the GUUC sequence, which is converted to GTΨC (Ψ = pseudouridine) in most tRNAs. This type of tRNA editing is different from other, previously described types of tRNA editing and resembles the mRNA and rRNA editing in
Physarum
and
Didymium
. Analogous tRNAs in
Physarum
and
Didymium
have editing sites at different locations, indicating that editing sites have been lost, gained, or both since the divergence of
Physarum
and
Didymium
. Although cDNAs derived from single tRNAs are generally fully edited, cDNAs derived from unprocessed polycistronic tRNA precursors often lack some of the editing site insertions. This enrichment of partially edited sequences in unprocessed tRNAs may indicate that editing is required for tRNA processing or at least that RNA editing occurs as an early event in tRNA synthesis.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
47 articles.
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