ArticlePlant cell reports2004
Cloning and expression of 1-aminocyclopropane-1-carboxylate synthase cDNA from rosa (Rosa x hybrida).
Article in Plant cell reports, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
9 citing papers in PubMed, 48 citations in OpenAlex.
- Determination of Flavonoids and Carotenoids and Their Contributions to Various Colors of Rose Cultivars (Frontiers in plant science · 2019Article
- Molecular aspects of flower senescence and strategies to improve flower longevity.Breeding science · 2018Review
- Genetics and genomics of flower initiation and development in roses.Journal of experimental botany · 2013Review
- Integrative analysis of miRNA and mRNA profiles in response to ethylene in rose petals during flower opening.PloS one · 2013Article
- Effects of abscisic acid on ethylene biosynthesis and perception in Hibiscus rosa-sinensis L. flower development.Journal of experimental botany · 2011Article
- Relationship between Rh-RTH1 and ethylene receptor gene expression in response to ethylene in cut rose.Plant cell reports · 2010Article
- Rh-PIP2;1, a rose aquaporin gene, is involved in ethylene-regulated petal expansion.Plant physiology · 2008Article
- Multiple models for Rosaceae genomics.Plant physiology · 2008Review
- Expression of ethylene biosynthetic and receptor genes in rose floral tissues during ethylene-enhanced flower opening.Journal of experimental botany · 2008Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The role of 1-aminocyclopropane-1-carboxylate (ACC) synthase in rose flower petal senescence was investigated. A cDNA library from senescing petals of rose ( Rosa x hybrid cv. Kardinal) prepared in lambdacDNA ZAP Express Vector was probed with a rose-specific 400-bp probe, and seven putative positive ACC synthase clones were isolated. Except for differences in length, the sequences of these clones were identical. A full-length clone, RKacc7, 1,750 bp long, coded for an open reading frame of 480 amino acids that contained the 11 conserved amino acid residues, the substrate and pyridoxal 5'-phosphate binding sites, all of which are characteristic of all ACC synthases. The transcripts prepared in vitro from the full-length clone when translated in rabbit reticulocyte lysates exhibited a 55-KDa polypeptide that comigrated with a polypeptide synthesized from a mRNA fraction isolated from senescing petals, and both were immunoselected by anti-ACC synthase antibodies. Reverse transcriptase-PCR-based studies showed that in planta RKacc7 is specifically expressed in rose petals, ovary and sepals. The expression of ACC synthase increased dramatically as the flower matured to senescence and also correlated positively with ethylene levels. The results of genomic Southern blots probed with RKacc7 are consistent with a pattern expected from a multigene family.
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