https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

园艺学报 ›› 2013, Vol. 40 ›› Issue (7): 1375-1381.

• 研究报告 • 上一篇    下一篇

黄瓜无侧枝基因nlb 的初步定位

任国良,杨绪勤,何欢乐,蔡 润,潘俊松*   

  1. 上海交通大学农业与生物学院,上海 200240
  • 收稿日期:2013-01-31 出版日期:2013-07-25 发布日期:2013-07-25
  • 基金资助:

    国家自然科学基金项目(31071081);国家重点基础研究发展计划项目(2012CB113900)

Genetic Mapping of the Non-lateral Branch Gene(nlb)in Cucumber

REN Guo-liang,YANG Xu-qin,HE Huan-le,CAI Run,and PAN Jun-song*   

  1. School of Agriculture and Biology,Shanghai Jiao Tong University,Shanghai 200240,China
  • Received:2013-01-31 Online:2013-07-25 Published:2013-07-25

摘要: 以黄瓜无侧枝品系419(P1)和有侧枝品系SB-2(P2)为亲本构建的136 株F2 群体为试验材料,对黄瓜无侧枝基因nlb 进行定位研究。田间调查和遗传分析结果表明,F2 群体的表现型中有侧枝与无侧枝的分离比为3︰1。运用分离群体分组混合分析法(bulked segregant analysis,BSA),从F2 无侧枝群体和有侧枝群体中各随机选取10 株,分别混合其DNA,构建无侧枝和有侧枝基因池,通过分析SSR分子标记在基因池间的多态性,筛选得到nlb 基因连锁标记9 个。然后利用F2 群体进行进一步验证,经MAPMAKER3.0 软件分析,将nlb 基因定位于黄瓜1 号染色体,其中距离nlb 基因较为紧密的标记是SSR19673,遗传距离为15.9 cM。

关键词: 黄瓜, 无侧枝基因nlb, 基因定位, SSR 标记

Abstract: A F2 population including 136 individuals derived from the crossing of non-lateral branch line 419(P1)and branch line SB-2(P2),using this F2 population as materials to research on non-lateral branch(nlb)gene mapping of cucumber. We found that F2 population may be divided into lateral branch
individuals and none lateral branch individuals by field investigation and genetic analysis,and their proportion fit for 3︰1. Constructing none branch and branch gene pools by taking bulked segregant analysis(BSA)which select 10 individuals from F2 non-branch population and branch population
randomly and mix their DNA respectively. We found 9 simple sequence repeat(SSR)markers which have polymorphism between two gene pools was linked to nlb gene. The F2 population was used on further verification and found molecular marker SSR19673 which is closer to nlb gene with genetic distance 15.9 cM through analysis of software MAPMAKER 3.0,therefore,nlb gene was mapped on the first chromosome of cucumber.

Key words: cucumber, nlb gene, gene mapping, SSR marker

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