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Mol. Cell. Biol., 12 1997, 6948-6952, Vol 17, No. 12
ML Reed and MR Hanson
Single nucleotides in plant chloroplast transcripts are edited from the
genomically encoded C to U, often resulting in changes of the encoded
protein sequence. Site-specific trans-acting factors are postulated to
direct the selection of edited residues. In order to further define cis
sequences required for RNA editing, we investigated whether two editing
sites present in maize rpoB mRNA would be recognized by the editing
machinery of transformed tobacco chloroplasts. A 93-nucleotide (nt) segment
surrounding site I is sufficient to direct editing of the maize sequence in
tobacco chloroplasts. However, an 86-nt segment surrounding maize site IV
(which is genomically encoded as a T in tobacco) does not confer editing of
this site, suggesting that trans-acting factors necessary for recognition
of site IV are not present in tobacco. The maize sequences surrounding site
I were found to compete with the endogenous rpoB for a depletable trans
factor and to reduce editing of endogenous site I. The presence of
exogenous maize site I was also found to decrease editing of endogenous
tobacco site II, indicating that there is a shared aspect of editing for
some closely spaced editing sites.
Copyright © 1997, American Society for Microbiology
A heterologous maize rpoB editing site is recognized by transgenic tobacco chloroplasts
Section of Genetics and Development, Cornell University, Ithaca, New York 14853, USA.
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