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龙眼‘蜀冠’ב大乌圆’杂交后代果实品质性状多样性分析及综合评价
引用本文:薛 鑫,石胜友,侯世奎.龙眼‘蜀冠’ב大乌圆’杂交后代果实品质性状多样性分析及综合评价[J].园艺学报,2020,36(5):827-836.
作者姓名:薛 鑫  石胜友  侯世奎
作者单位:1岭南师范学院生命科学与技术学院,广东湛江 524048;2中国热带农业科学院南亚热带作物研究所,农业部热带果树生物学重点实验室,广东湛江 524091;3海南大学园艺学院,海口 570100;4重庆市储美果树研究所,重庆 402260
基金项目:国家自然科学基金项目(31572087);广东省自然科学基金项目(2020A1515011365);国家现代农业产业技术体系建设专项资金项目(CARS-32-02);中国热带农业科学院基本科研业务费项目(1630062020003)
摘    要:以龙眼‘蜀冠’ב大乌圆’的F1代65个单株为材料,对其果实的27个品质性状进行了连续3年的观测,应用SPSS19.0软件对各性状进行变异系数、Shannon-Weinner多样性指数和主成分分析。结果表明:65个单株果实品质性状存在着极显著差异,13个数量性状(单果质量、果实纵径、果实横径、可溶性固形物、可食率、果皮厚度、果皮质量、果肉厚、种子质量、维生素C含量、蔗糖含量、葡萄糖含量和果糖含量)变异系数在6.95% ~ 41.64%之间;多样性指数在1.33 ~ 2.02之间;14个描述性状(成熟期、果皮颜色、果形、果肩、果顶、龟裂纹、疣状突起、果肉颜色、果肉质地、果肉透明度、果肉离核难易度、果汁、化渣程度和果肉风味)多样性指数在0.56 ~ 1.28之间;主成分分析发现前5个性状(单果质量、可食率、可溶性固形物、成熟期和果实风味)的累积贡献率为87.50%;建立了‘蜀冠’ב大乌圆’杂交后代果实品质性状综合评价的方法,利用该方法在65个杂交后代中筛选出了5个优异的单株(SD7、SD11、SD36、SD53和SD120),结果与实际观测结果高度一致。

关 键 词:龙眼  杂交后代  果实品质性状  多样性  综合评价  

Specific expression of hyperpolarization-activated cyclic nucleotide-ga-ted cation channel isoforms in rat superficial spinal dorsal horn
HUANG Jiao-yan,CHENG Xiao-e,MA Long-xian,ZHANG Da-ying,JIANG Chang-yu,LIU Tao.Specific expression of hyperpolarization-activated cyclic nucleotide-ga-ted cation channel isoforms in rat superficial spinal dorsal horn[J].Acta Horticulturae Sinica,2020,36(5):827-836.
Authors:HUANG Jiao-yan  CHENG Xiao-e  MA Long-xian  ZHANG Da-ying  JIANG Chang-yu  LIU Tao
Institution:1.School of Life and Technology of Lingnan Normal University,Zhanjiang,Guangdong 524048,China;2Key Laboratory of Tropical Fruit Biology,Ministry of Agriculture,South Subtropical Crops Research Institute,Chinese Academy of Tropical Agricultural Sciences,Zhanjiang,Guangdong 524091,China;3College of Horticulture and Landscape Architecture,Hainan University,Haikou 570100,China;4Chumei Subtropical Fruit Trees Research Institute,Chongqing 402260,China
Abstract:AIMTo investigate the distinct expression and localization of the 4 subtypes of hyperpolarization-activated cyclic nucleotide-gated cation (HCN) channels in rat superficial spinal dorsal horn (SDH). METHODSTransverse slices of L4~L5 segments were obtained from Sprague-Dawley (SD) rats (3~5-week-old) of either sex. Using the immunohistochemical technique and laser confocal imaging, the distribution of HCN1~4 in neurons, glia cells and subcellular structure of neuron in SDH was observed. RESULTSThe expression of 4 subtypes of HCN channel in rat SDH was distinct: HCN1 was mainly co-localized with neuronal marker neuronal nuclei (NeuN) and astrocyte marker glial fibrillary acidic protein (GFAP). HCN2 and HCN3 were largely co-localized with NeuN. HCN2 was primarily co-localized with peptidergic primary afferent nerve ending marker calcitonin gene-related peptide (CGRP). However, HCN4 was mainly co-localized with non-peptidergic primary afferent nerve ending marker isolectin B4 (IB4). HCN1 and HCN4 were mainly co-localized with dendrite marker microtubule-associated protein 2 (MAP2). HCN4 was primarily co-localized with axonal terminal of inhibitory interneuron marker vesicular γ-aminobutyric acid transporter (VGAT). CONCLUSION HCN1~4 are predominantly distributed in superficial spinal dorsal horn and exhibit a specific expression pattern in neurons, glia cells and subcellular structure of neurons.
Keywords:Hyperpolarization-activated cyclic nucleotide-gated cation channels  Spinal dorsal horn  Neurons  
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