Abstract
Several clones corresponding to the gene encoding NADH-dependent hydroxypyruvate reductase have been isolated from a cucumber genomic library. Restriction mapping indicates the presence of two HPR genes, hpr-A and hpr-B, in the cucumber genome. Examination of the DNAs of individual plants suggests that hpr-A and hpr-B are most likely alleles at a single locus. The sequence of a 6.7 kb genomic fragment that includes the entire transcribed region, 2.2 kb of 5' flanking sequence, and about 0.8 kb of 3' flanking sequence reveals the presence of 12 introns in hpr-A. These introns are AT-rich relative to the exons. The donor sequence at the 5' end of the sixth intron contains an unusual dinucleotide, GC, rather than the nearly invariant GT. Primer extension analysis maps the transcription initiation site to 61 nucleotides upstream of the translation initiation codon. An AT-rich stretch is centered at position -31 with respect to the transcription initiation site, and a potential CCAAT box is centered at position -138. Several elements that are homologous to regulatory elements of other plant genes have been identified in the flanking regions of hpr-A.
MeSH Terms
Alcohol Oxidoreductases/genetics
Amino Acid Sequence
Base Sequence
Blotting, Southern
Cloning, Molecular
Gene Expression Regulation/physiology
Hydroxypyruvate Reductase
Introns/genetics
Light
Molecular Sequence Data
Plant Proteins/genetics
Plants/enzymology,genetics
Plants, Genetically Modified/genetics
Plants, Toxic
Restriction Mapping
Tobacco/genetics
Chemicals
Plant Proteins
Alcohol Oxidoreductases
Hydroxypyruvate Reductase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schwartz B W
Department of Genetics, University of Wisconsin, Madison 53706.
Sloan J S
Becker W M
References (13)
13 references, click to expand
-
Mapping of gene transcripts by nuclease protection assays and cDNA primer extension.
Methods Enzymol. 1987;152:611-32
PMID: 2821358
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
Anal Biochem. 1983 Jul 1;132(1):6-13
PMID: 6312838
-
The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.
Nucleic Acids Res. 1989 Mar 25;17(6):2159-80
PMID: 2704616
-
A catalogue of splice junction and putative branch point sequences from plant introns.
Nucleic Acids Res. 1986 Dec 22;14(24):9549-59
PMID: 3808952
-
Photoregulated gene expression may involve ubiquitous DNA binding proteins.
EMBO J. 1990 Nov;9(11):3415-27
PMID: 2209551
-
Light-stimulated accumulation of the peroxisomal enzymes hydroxypyruvate reductase and serine:glyoxylate aminotransferase and their translatable mRNAs in cotyledons of cucumber seedlings.
Plant Mol Biol. 1987 May;9(3):259-75
PMID: 24276974
-
Isolation, characterization and sequence analysis of a full-length cDNA clone encoding NADH-dependent hydroxypyruvate reductase from cucumber.
Plant Mol Biol. 1989 Aug;13(2):139-50
PMID: 2519111
-
Organ Specificity and Light Regulation of NADH-Dependent Hydroxypyruvate Reductase Transcript Abundance.
Plant Physiol. 1990 Nov;94(3):1484-7
PMID: 16667858
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
Anal Biochem. 1987 Apr;162(1):156-9
PMID: 2440339
-
Unidirectional digestion with exonuclease III in DNA sequence analysis.
Methods Enzymol. 1987;155:156-65
PMID: 3323819
-
Molecular light switches for plant genes.
Plant Cell. 1990 May;2(5):369-78
PMID: 2152164
-
Organization and expression of eucaryotic split genes coding for proteins.
Annu Rev Biochem. 1981;50:349-83
PMID: 6791577
-
Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing.
J Mol Biol. 1980 Oct 25;143(2):161-78
PMID: 6260957