您的位置: 专家智库 > >

国家自然科学基金(31030056)

作品数:2 被引量:11H指数:1
相关作者:朱婕刘志勇孙其信华为杨作民更多>>
相关机构:中国农业大学更多>>
发文基金:国家自然科学基金长江学者和创新团队发展计划国家高技术研究发展计划更多>>
相关领域:农业科学生物学更多>>

文献类型

  • 2篇中文期刊文章

领域

  • 2篇农业科学
  • 1篇生物学

主题

  • 1篇短柄草
  • 1篇小麦
  • 1篇小麦抗白粉病...
  • 1篇抗白粉病
  • 1篇抗白粉病基因
  • 1篇基因
  • 1篇基因组
  • 1篇基因组学
  • 1篇共线性
  • 1篇二穗短柄草
  • 1篇白粉
  • 1篇白粉病
  • 1篇比较基因组
  • 1篇比较基因组学
  • 1篇REVEAL...
  • 1篇BL
  • 1篇COMPAR...
  • 1篇EST
  • 1篇GENOMI...
  • 1篇SAME

机构

  • 1篇中国农业大学

作者

  • 1篇刘子记
  • 1篇杨作民
  • 1篇华为
  • 1篇孙其信
  • 1篇刘志勇
  • 1篇朱婕

传媒

  • 1篇作物学报
  • 1篇Journa...

年份

  • 1篇2015
  • 1篇2011
2 条 记 录,以下是 1-2
排序方式:
小麦抗白粉病基因pm42的EST连锁图谱构建和比较基因组学分析被引量:10
2011年
目的基因精细遗传连锁图谱的构建是图位克隆的基础,小麦功能基因精细遗传连锁图谱的构建依赖于比较基因组学分析。水稻和短柄草(Brachypodium distachyon)基因组序列是小麦比较基因组学分析和功能基因精细遗传定位的重要工具。本研究利用小麦、短柄草和水稻的基因组共线性关系对小麦抗白粉病基因pm42进行比较基因组学分析,明确了pm42基因所在2BS基因组区域与短柄草第1染色体和水稻第3染色体直系同源基因组区域的对应关系,开发出与抗白粉病基因pm42连锁的EST-SSCP(expressed sequence tag-single strand conformation polymorphism)标记CD452782和BF201235,以及EST-STS(expressed sequence tag-sequence tagged site)标记CJ674042、EB513371和CV771633,构建了pm42基因EST标记遗传连锁图谱,CJ674042、BF201235、CD452782和CV771633位于pm42近端粒侧,距离pm42的遗传距离分别为1.9、12.0、19.7和25.7cM;EB513371位于pm42近着丝粒侧,与pm42的遗传距离为14.6cM。整合原有的作图数据,构建了pm42基因的高密度比较基因组学遗传连锁图谱,pm42被定位于3.3cM的区间,该区间对应于短柄草66kb的基因组区域及水稻69kb的基因组区域。该结果为抗白粉病基因pm42高密度精细遗传连锁图谱构建、分子辅助选择和基因聚合奠定了基础。
刘子记朱婕华为杨作民孙其信刘志勇
关键词:小麦抗白粉病基因比较基因组学二穗短柄草共线性
Comparative genetic mapping revealed powdery mildew resistance gene MlWE4 derived from wild emmer is located in same genomic region of Pm36 and Ml3D232 on chromosome 5BL被引量:1
2015年
Powdery mildew, caused by Blumeria graminis f. sp. tritici, is one of the most devastating wheat diseases. Wild emmer wheat(Triticum turgidum ssp. dicoccoides) is a promising source of disease resistance for wheat. A powdery mildew resistance gene conferring resistance to B. graminis f. sp. tritici isolate E09, originating from wild emmer wheat, has been transferred into the hexaploid wheat line WE4 through crossing and backcrossing. Genetic analyses indicated that the powdery mildew resistance was controlled by a single dominant gene, temporarily designated Ml WE4. By mean of comparative genomics and bulked segregant analysis, a genetic linkage map of Ml WE4 was constructed, and Ml WE4 was mapped on the distal region of chromosome arm 5BL. Comparative genetic linkage maps showed that genes Ml WE4, Pm36 and Ml3D232 were co-segregated with markers XBD37670 and XBD37680, indicating they are likely the same gene or alleles in the same locus. The co-segregated markers provide a starting point for chromosome landing and map-based cloning of Ml WE4, Pm36 and Ml3D232.
ZHANG DongOUYANG Shu-hongWANG Li-liCUI YuWU Qiu-hongLIANG YongWANG Zhen-zhongXIE Jing-zhongZHANG De-yunWANG YongCHEN Yong-xingLIU Zhi-yong
共1页<1>
聚类工具0