Fine mapping of qhir1 influencing in vivo haploid induction in maize

被引:76
作者
Dong, X. [1 ]
Xu, X. [1 ]
Miao, J. [1 ]
Li, L. [1 ]
Zhang, D. [1 ]
Mi, X. [2 ]
Liu, C. [1 ]
Tian, X. [1 ]
Melchinger, A. E. [2 ]
Chen, S. [1 ,3 ]
机构
[1] China Agr Univ, Natl Maize Improvement Ctr China, Beijing 100193, Peoples R China
[2] Univ Hohenheim, Inst Plant Breeding Seed Sci & Populat Genet, D-70593 Stuttgart, Germany
[3] China Agr Univ, Beijing Key Lab Crop Genet Improvement, Beijing 100193, Peoples R China
基金
比尔及梅琳达.盖茨基金会;
关键词
QUANTITATIVE TRAIT LOCUS; SEGREGATION DISTORTION; MATERNAL HAPLOIDS; SELECTION; INDUCERS; MARKER; LINES; GENE;
D O I
10.1007/s00122-013-2086-9
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Production of haploids by the in vivo haploid induction method has now become routine for generating new inbred lines in maize. In previous studies, a major quantitative trait locus (QTL) (qhir1) located in bin 1.04 was detected, explaining up to 66 % of the genotypic variance for haploid induction rate (HIR). Our objectives were to (1) fine-map qhir1 and (2) identify closely linked markers useful for marker-assisted breeding of new inducers. For this purpose, we screened a mapping population of 14,375 F-2 plants produced from a cross between haploid inducer UH400 and non-inducer line 1680 to identify recombinants. Based on sequence information from the B73 reference genome, markers polymorphic between the two parents were developed to conduct fine mapping with these recombinants. A progeny test mapping strategy was applied to accurately determine the HIR of the 14 recombinants identified. Furthermore, F-3 progeny of recombinant F-2 plants were genotyped and in parallel evaluated for HIR. We corroborated earlier studies in that qhir1 has both a significantly positive effect on HIR but also a strong selective disadvantage, as indicated by significant segregation distortion. Altogether, we were able to narrow down the qhir1 locus to a 243 kb region flanked by markers X291 and X263.
引用
收藏
页码:1713 / 1720
页数:8
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