首页 | 本学科首页   官方微博 | 高级检索  
     

应用分子标记研究水稻根系形态特征数量性状位点
引用本文:方萍 吴平. 应用分子标记研究水稻根系形态特征数量性状位点[J]. 作物学报, 1999, 25(2): 181-185
作者姓名:方萍 吴平
作者单位:浙江农业大学土壤与农业化学系,浙江杭州,310029
基金项目:浙江省自然科学基金资助项目
摘    要:通过水培试验测定水稻F3群体((Palawan×IR42)137株系的幼苗根体积、根表面积、相对根粗、最大根长和根数等根系形态特征。借助由该组合的F2群体所构建的RFLP标记连锁图,通过方差分析检测与根系形态特征表型值相关连的分子标记位点,共测得7个标记位点分别与3个表型性状关连。其中位于2号染色体上的2对连锁标记位点RG139与RZ

关 键 词:水稻  根系形态特征  数量性状位点
收稿时间:1998-02-07
修稿时间:1998-07-14

QTLs for Rice Root Morphological Characters
Fang Ping Wu Ping Tao Qinnan. QTLs for Rice Root Morphological Characters[J]. Acta Agronomica Sinica, 1999, 25(2): 181-185
Authors:Fang Ping Wu Ping Tao Qinnan
Affiliation:Department of Soil and Agrochemistry, Zhejiang Agricultural University, Hangzhou, 310029
Abstract:One hundred and thirty seven F3 families developed from an F2 population derived from a cross between a japonica variety, Palawan and an indica variety, IR42 were used in a solution experiment to investigate the root morphological characters including root volume (RV), root surface area(RSA), relative root thickness(RRT), maximum root length(MRL) and root number (RN). One hundred and four molecular markers mapped on all 12 chromosomes based on the F2 population were used to detect markers associated with the variations in the root characters. Two linked marker loci RZ724 and RG139 on chromosome 2 were detected to be significantly associated with both RV and MRL; the variantions in RV and MRL were also significantly associated with two linked marker loci RG171 and RG544 on chromosome 2, and with marker loci RG13 and RG229 on chromosome 5, respectively. Only one marker locus CDO105 on chromosome 5 was found to be significantly associated with RRT. Mean comparisons between different marker genotypes at the loci detected indicate significant additive effects on the three root characters. No marker loci were found to be significantly associated with other two characters in this cace.
Keywords:Oryza sativa L.  Root morphological characters  QTLs
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《作物学报》浏览原始摘要信息
点击此处可从《作物学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号