allelic variations of a light harvesting chlorophyll ab-binding protein gene (lhcb1) associated with agronomic traits in barley等位基因变异的光收获叶绿素ab-binding蛋白基因(lhcb1)与大麦农艺性状有关.pdfVIP

allelic variations of a light harvesting chlorophyll ab-binding protein gene (lhcb1) associated with agronomic traits in barley等位基因变异的光收获叶绿素ab-binding蛋白基因(lhcb1)与大麦农艺性状有关.pdf

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allelic variations of a light harvesting chlorophyll ab-binding protein gene (lhcb1) associated with agronomic traits in barley等位基因变异的光收获叶绿素ab-binding蛋白基因(lhcb1)与大麦农艺性状有关

Allelic Variations of a Light Harvesting Chlorophyll A/B- Binding Protein Gene (Lhcb1) Associated with Agronomic Traits in Barley 1,2 2 3 1 4 4 Yanshi Xia , Zhengxiang Ning , Guihua Bai , Ronghua Li , Guijun Yan , Kadambot H. M. Siddique , 5 1 Michael Baum , Peiguo Guo * 1 International Crop Research Center for Stress Resistance, College of Life Sciences, Guangzhou University, Guangzhou, China, 2 College of Light Industry and Food Science, South China University of Technology, Guangzhou, China, 3 Hard Winter Wheat Genetics Research Unit, United States Department of Agriculture - Agricultural Research Service, Manhattan, Kansas, United States of America, 4 The Institute of Agriculture, The University of Western Australia, Crawley, Perth, Australia, 5 International Center for Agricultural Research in the Dry Areas, Aleppo, Syria Abstract Light-harvesting chlorophyll a/b-binding protein (LHCP) is one of the most abundant chloroplast proteins in plants. Its main function is to collect and transfer light energy to photosynthetic reaction centers. However, the roles of different LHCPs in light-harvesting antenna systems remain obscure. Exploration of nucleotide variation in the genes encoding LHCP can facilitate a better understanding of the functions of LHCP. In this study, nucleotide variations in Lhcb1, a LHCP gene in barley, were investigated across 292 barley accessions collected from 35 different countries using EcoTILLING technology, a variation of the Targeting Induced Local Lesions In Genomes (TILLING). A total of 23 nucleotide variations were detected including three insert/deletions (indels) and 20 single nucleotide polymorphisms (SNPs). Among them, 17

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