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TaDEP1基因在普通六倍体小麦及其供体种中的保守与分化
引用本文:毛龙,张锴,张兰,李爱丽,赵光耀,孔秀英,贾继增,徐吉臣.TaDEP1基因在普通六倍体小麦及其供体种中的保守与分化[J].植物遗传资源学报,2011,12(6):957-964.
作者姓名:毛龙  张锴  张兰  李爱丽  赵光耀  孔秀英  贾继增  徐吉臣
作者单位:1. 北京林业大学生物科学与技术学院/林木育种国家工程实验室/林木、花卉遗传育种教育部重点实验室/国家林业局树木花卉育种与生物工程重点开放实验室,北京100083;中国农业科学院作物科学研究所/国家农作物基因资源与基因改良重大科学工程,北京100081
2. 中国农业科学院作物科学研究所/国家农作物基因资源与基因改良重大科学工程,北京,100081
3. 北京林业大学生物科学与技术学院/林木育种国家工程实验室/林木、花卉遗传育种教育部重点实验室/国家林业局树木花卉育种与生物工程重点开放实验室,北京,100083
基金项目:The National Basic Research Program of China (973 Program)
摘    要:根据已知小麦正源基因TaDEP1 cDNA序列设计引物,成功克隆了小麦TaDEP1基因组序列,发现该基因包含5个外显子,4个内含子.通过比较该基因在六倍体普通小麦A、B、D基因组中的差异,筛选出可以区分A、B、D基因组的分子标记Ta956.以中国春缺体-四体系为材料,利用该标记将TaDEP1基因定位于小麦5A、5B和5...

关 键 词:小麦  TaDEP1  染色体定位  序列分析
收稿时间:1/28/2011 8:29:44 AM
修稿时间:8/13/2011 5:38:44 PM

Conservation and divergence of TaDEP1 genes in common wheat (Triticum aestivum L.) and its donor species
Mao Long,Zhang Lan,and.Conservation and divergence of TaDEP1 genes in common wheat (Triticum aestivum L.) and its donor species[J].Journal of Plant Genetic Resources,2011,12(6):957-964.
Authors:Mao Long  Zhang Lan  and
Institution:ZHANG Kai1,2,LI Ai-li2,ZHANG Lan2,ZHAO Guang-yao2,KONG Xiu-ying2,JIA Ji-zeng2,XU Ji-chen1,MAO Long2(1National Engineering Laboratory for Tree Breeding/Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants,Ministry of Education/The Tree and Ornamental Plant Breeding and Biotechnology Laboratory of State Forestry Administration/College of Biological Sciences and Biotechnology Beijing Forestry University,Beijing 100083,2 National Key Facility for Crop Gene Resources and Genetic Improve...
Abstract:The rice DEP1 (DENSE AND ERECT PANICLE1) gene is an important regulator that can enhance meristematic activity, reduce internode distance, increase per spike grain number, and eventually increase the rice yield. We report here the cloning of the genomic sequence of the wheat orthologous gene TaDEP1 which contains five exons and 4 introns. Genomic sequence comparison revealed a region that can be used as molecular marker (Ta956) to distinguish homoeoalleles of hexaploid wheat. Ta956 was used to map TaDEP1 to wheat chromosomes 5A, 5B, and 5D by using Chinese Spring nulli-tetrasomic lines. Sequences corresponding to Ta956 were then isolated and sequenced from hexaploid wheat, its putative donor species and tetraploid wheat. Sequence comparison showed that most variations were present at introns, particularly between the B and D homoeoalleles. Domain analysis showed that proteins from the D genome of hexaploid wheat was more different to those on the A and D genomes, suggesting functional divergence among TaDEP1 proteins from the A, B, and D genomes. The potential of using Ta956 as a marker for variety identification is discussed.
Keywords:Triticum aestivum  TaDEP1  Chromosomal localization  sequence analysis
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