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      Gene-flow investigation between garden and wild roses planted in close distance

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          Abstract

          Rose is a major ornamental plant, and a lot of cultivars with attractive morphology, color and scent have been generated by classical breeding. Recent progress of genetic modification produces a novel cultivar with attractive features. In both cases, a major problem is the gene-flow from cultivated or genetically modified (GM) plants to wild species, causing reduction of natural population. To investigate whether gene-flow occurs in wild species, molecular analysis with DNA markers with higher efficient technique is useful. Here we investigated the gene-flow from cultivated roses ( Rosa× hybrida) to wild rose species planted in close distance in the field. The overlapping flowering periods and visiting insects suggest that pollens were transported by insects between wild and cultivated roses. We examined the germination ratio of seeds from wild species, and extracted DNA and checked with KSN and APETALA2 ( AP2) DNA markers to detect transposon insertions. Using two markers, we successfully detected the outcross between wild and cultivated roses. For higher efficiency, we established a bulking method, where DNA, leaves or embryos were pooled, enabling us to that check the outcross of many plants. Our results suggest that wild species and garden cultivars can cross in close distance, so that they should be planted in distance, and checked the outcross with multiple DNA markers.

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          The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors.

          Mutations in the homeotic gene agamous of the plant Arabidopsis cause the transformation of the floral sex organs. Cloning and sequence analysis of agamous suggest that it encodes a protein with a high degree of sequence similarity to the DNA-binding region of transcription factors from yeast and humans and to the product of a homeotic gene from Antirrhinum. The agamous gene therefore probably encodes a transcription factor that regulates genes determining stamen and carpel development in wild-type flowers.
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            A simple and rapid method for the preparation of plant genomic DNA for PCR analysis.

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              The Rosa genome provides new insights into the domestication of modern roses

              Roses hold high cultural and economic importance as ornamentals and for the perfume industry. We report the rose whole genome sequencing and assembly and resequencing of major genotypes that contributed to rose domestication. We generated a homozygous genotype from a heterozygous diploid modern roses progenitor, Rosa chinensis ‘Old Blush’. Using Single Molecule Real-Time sequencing and a meta-assembly approach we obtained one of the most complete plant genomes to date. Diversity analyses highlighted the mosaic origin of ‘La France’, one of the first hybrids combining the growth vigor of European species and recurrent blooming of Chinese species. Genomic segments of Chinese ancestry revealed new candidate genes for recurrent blooming. Reconstructing regulatory and secondary metabolism pathways allowed us to propose a model of interconnected regulation of scent and flower color. This genome provides a foundation for understanding the mechanisms governing rose traits and will accelerate improvement in roses, Rosaceae and ornamentals.
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                Author and article information

                Journal
                Plant Biotechnol (Tokyo)
                Plant Biotechnol (Tokyo)
                plantbiotechnol
                Plant Biotechnology
                Japanese Society for Plant Biotechnology (c/o Academy Center, Yamabukicho 358-5, Shinjuku-ku, Tokyo 162-0801, Japan )
                1342-4580
                1347-6114
                25 December 2023
                : 40
                : 4
                : 283-288
                Affiliations
                [1 ]Department of Agricultural and Life Science, Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Shimogamo Hangi-cho, Sakyo-ku, Kyoto 606-8522, Japan
                [2 ]Research Institute, Suntory Global Innovation Center Ltd., Seikadai 8-1-1, Seika-cho, Kyoto 619-0284, Japan
                [3 ]Biotechnology Research Department, Kyoto Prefectural Agriculture, Forestry and Fisheries Technology Center, Kitaina Yazuma Oji 74, Seika-cho, Kyoto 619-0244, Japan
                Author notes
                [*] [* ]E-mail: seijitakeda@ 123456kpu.ac.jp Tel: +81-774-93-3526
                Article
                10.5511/plantbiotechnology.23.0708a
                10905366
                38434113
                7e29b16a-0be6-461b-8b6b-db26efd8255d
                © 2023 Japanese Society for Plant Biotechnology

                This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, https://creativecommons.org/licenses/by/4.0/).

                History
                : 12 April 2023
                : 8 July 2023
                Categories
                Original Paper

                apetala2,dna marker,gene-flow,ksn,rose
                apetala2, dna marker, gene-flow, ksn, rose

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