Bicheng Dun
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Bicheng Dun has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
- Guiyun Huang
Yangtze River Biodiversity Research Centre, China Three Gorges Corporation, China
2 shared publications - Haibo Zhang
Yangtze River Biodiversity Research Centre, China Three Gorges Corporation, Wuhan 443133, China
2 shared publications - Di He
Engineering Research Center of Eco-Environment in Three Gorges Reservoir Region, Ministry of Education, Hubei International Scientific and Technological Center of Ecological Conservation and Management in the Three Gorges Area, China Three Gorges University, Yichang 443002, China
1 shared publication - Di Wu
Hubei Key Laboratory of Rare Resource Plants in Three Gorges Reservoir Area, China Three Gorges Corporation, Yichang 443100, China
1 shared publication - Di Wu
Rare Plants Research Institute of Yangtze River, Three Gorges Corporation, Yichang 443000, China
1 shared publication - Guoli Li
Beijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, College of Horticulture, China Agricultural University, Beijing 100193, China
1 shared publication
Latest Publications
- Open Access
Chromosome-Level Genome Assembly of Myricaria laxiflora and Identification of Candidate MylAP2/ERF Genes Involved in Flooding Stress
M. laxiflora is an endangered plant that grows in the Yangtze River floodplain of China and often suffers from flooding stress. Due to the lack of a reference genome for M. laxiflora, the molecular regulatory mechanism of waterlogging stress in this plant remains unclear. In this study, we report a high-quality reference genome of M. laxiflora with a size of 1.29 Gb. A total of 23,666 gene-encoding proteins and 5457 ncRNAs were predicted in this reference genome. A comparative genome analysis revealed that 902 and 4299 gene families significantly expanded and contracted, respectively, in M. laxiflora. The expansions of the 902 gene families were significantly related to the “response to stress”, “response to abiotic stimulus”, and “response to oxygen-containing compounds” pathways. In the M. laxiflora genome, 101 MylAP2/ERF genes were identified and divided into five subgroups. Several MeJA-, ABA-, and hypoxia-responsive elements were found in the promoter regions of these MylAP2/ERF genes. According to the transcriptome data analysis, 74 MylAP2/ERF genes responded to flooding stress. Moreover, three genes (MylAP2/ERF49/78/91) that belong to the same branch as the RAP2.2 gene exhibited different expression trends under flooding stress. Our results provide valuable information on the molecular regulatory mechanism of flooding stress in M. laxiflora.
Open AccessChromosome-Level Genome Assembly of Myricaria laxiflora and Identification of Candidate MylAP2/ERF Genes Involved in Flooding Stress
M. laxiflora is an endangered plant that grows in the Yangtze River floodplain of China and often suffers from flooding stress. Due to the lack of a reference genome for M. laxiflora, the molecular regulatory mechanism of waterlogging stress in this plant remains unclear. In this study, we report a high-quality reference genome of M. laxiflora with a size of 1.29 Gb. A total of 23,666 gene-encoding proteins and 5457 ncRNAs were predicted in this reference genome. A comparative genome analysis revealed that 902 and 4299 gene families significantly expanded and contracted, respectively, in M. laxiflora. The expansions of the 902 gene families were significantly related to the “response to stress”, “response to abiotic stimulus”, and “response to oxygen-containing compounds” pathways. In the M. laxiflora genome, 101 MylAP2/ERF genes were identified and divided into five subgroups. Several MeJA-, ABA-, and hypoxia-responsive elements were found in the promoter regions of these MylAP2/ERF genes. According to the transcriptome data analysis, 74 MylAP2/ERF genes responded to flooding stress. Moreover, three genes (MylAP2/ERF49/78/91) that belong to the same branch as the RAP2.2 gene exhibited different expression trends under flooding stress. Our results provide valuable information on the molecular regulatory mechanism of flooding stress in M. laxiflora.
- Open Access
- 17 November 2022
- Published by MDPI AG in Sustainability
- Vol. 14 (22) , 15305
The Establishment of Rapid Propagation System of ‘RED SUN’ Phalaenopsis aphrodite
Phalaenopsis aphrodite Rchb. F. is a plant of great ornamental and economic value, and its growth has strict requirements in terms of environment. In order to establish the rapid propagation of Phalaenopsis aphrodite Rchb. F., this study used the popular large-flowered variety ‘RED SUN’, which is found on the market, as the material, and studied the effects of pedicel taking time, site, plant growth regulators, and organic substances on the establishment of a regeneration system. The results indicated that the best combination of initiation culture was collecting peduncles in January + upper position of peduncles + 0.1% HgCl2 sterilization for 8 min. The best recipe for inducing adventitious buds was MS + TDZ 0.4 mg/L + NAA 0.5 mg/L. The optimal combination for adventitious bud propagation was MS + TDZ 0.2 mg/L + NAA 0.4 mg/L. The best recipe for strong seedling from aseptic seedlings was MS + NAA 0.4 mg/L + banana powder 20 g/L + tryptone 2 g. The best recipe for rooting for aseptic seedlings was 1/2 MS + IBA 0.5 mg/L + charcoal 2 g/L. The best combination of acclimation and transplanting for Phalaenopsis was using sphagnum in the training seedling room, which produced a seedling survival rate of 97%. Our findings, therefore, demonstrate the methods of rapid breeding of the Phalaenopsis orchid, which provide a scientific basis for the conservation of this species.
- 17 November 2022
- Published by MDPI AG in Sustainability
- Vol. 14 (22) , 15305
Open AccessThe Establishment of Rapid Propagation System of ‘RED SUN’ Phalaenopsis aphrodite
Phalaenopsis aphrodite Rchb. F. is a plant of great ornamental and economic value, and its growth has strict requirements in terms of environment. In order to establish the rapid propagation of Phalaenopsis aphrodite Rchb. F., this study used the popular large-flowered variety ‘RED SUN’, which is found on the market, as the material, and studied the effects of pedicel taking time, site, plant growth regulators, and organic substances on the establishment of a regeneration system. The results indicated that the best combination of initiation culture was collecting peduncles in January + upper position of peduncles + 0.1% HgCl2 sterilization for 8 min. The best recipe for inducing adventitious buds was MS + TDZ 0.4 mg/L + NAA 0.5 mg/L. The optimal combination for adventitious bud propagation was MS + TDZ 0.2 mg/L + NAA 0.4 mg/L. The best recipe for strong seedling from aseptic seedlings was MS + NAA 0.4 mg/L + banana powder 20 g/L + tryptone 2 g. The best recipe for rooting for aseptic seedlings was 1/2 MS + IBA 0.5 mg/L + charcoal 2 g/L. The best combination of acclimation and transplanting for Phalaenopsis was using sphagnum in the training seedling room, which produced a seedling survival rate of 97%. Our findings, therefore, demonstrate the methods of rapid breeding of the Phalaenopsis orchid, which provide a scientific basis for the conservation of this species.