The maize mitochondrial cox2 gene has five promoters in two genomic regions, including a complex promoter consisting of seven overlapping units

Citation
Ds. Lupold et al., The maize mitochondrial cox2 gene has five promoters in two genomic regions, including a complex promoter consisting of seven overlapping units, J BIOL CHEM, 274(6), 1999, pp. 3897-3903
Citations number
31
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
274
Issue
6
Year of publication
1999
Pages
3897 - 3903
Database
ISI
SICI code
0021-9258(19990205)274:6<3897:TMMCGH>2.0.ZU;2-C
Abstract
Plant mitochondrial genes are often transcribed into complex sets of RNAs, resulting from multiple initiation sites and processing steps. To elucidate the role of initiation in generating the more than 10 cox2 transcripts fou nd in maize mitochondria, we surveyed sequences upstream of cox2 for active promoters. Because the cox2 coding region is immediately downstream of a 0 .7-kb recombination repeat, cox2 is under the control of two different sets of potential expression signals. Using an in vitro transcription assay, we localized four promoters upstream of the coding region in the so-called ma ster chromosome, and two promoters upstream of the coding region in the rec ombinant subgenome, Ribonuclease protection analysis of labeled primary tra nscripts confirmed that all but one of these promoters is active in vivo. P rimer extension was used to identify the promoter sequences and initiation sites, which agree with the consensus established earlier for maize mitocho ndria. This study identified two unusual promoters, the core sequences of w hich were composed entirely of adenines and thymines, and one of which was a complex promoter consisting of seven overlapping units. Deletion mutagene sis of the complex promoter suggested that each of its units was recognized independently by RNA polymerase, While each active promoter fit the maize core consensus sequence YRTAT, not all such sequences surveyed supported in itiation. We conclude that in vitro transcription is a powerful tool for lo cating mitochondrial promoters and that, in the case of cox2, promoter mult iplicity contributes strongly to transcript complexity.