He Jiwai, Shao Gaoneng, Wei Xiangjin, Huang Fenglin, Sheng Zhonghua, Tang Shaoqing, Hu Peisong
State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Hunan Rice Research Institute, Hunan Academy of Agricultural Science, Changsha, China.
PLoS One. 2017 May 25;12(5):e0178177. doi: 10.1371/journal.pone.0178177. eCollection 2017.
Rice tiller angle is an important agronomic trait that contributes to crop production and plays a vital role in high yield breeding. In this study, a recombinant inbred line (RIL) population derived from the cross of a glabrous tropical japonica rice D50 and an indica rice HB277, was used to investigate quantitative trait loci (QTLs) controlling rice tiller angle. Two major QTLs, qTAC8 and qTAC9, were detected. While qTAC9 mapped with a previously identified gene (TAC1), using a BC2F2 population qTAC8 was mapped to a 16.5 cM region between markers RM7049 and RM23175. Position of qTAC8 was narrowed to a 92 kb DNA region by two genetic segregating populations. Finally, one opening reading frame (ORF) was regarded as a candidate gene according to genomic sequencing and qRT-PCR analysis. In addition, a set of four near isogenic lines (NILs) were created to investigate the genetic relationship between those two QTLs, and one line carrying qTAC8 and qTAC9 presented additive effect of tiller angle, suggesting that these QTLs are involved in different genetic pathways. Our results provide a foundation for the cloning of qTAC8 and genetic improvement of the rice plant architecture.
水稻分蘖角度是一个重要的农艺性状,对作物产量有影响,在高产育种中起着至关重要的作用。本研究利用一个由无毛热带粳稻D50与籼稻HB277杂交衍生的重组自交系(RIL)群体,来研究控制水稻分蘖角度的数量性状基因座(QTL)。检测到两个主要的QTL,即qTAC8和qTAC9。虽然qTAC9与先前鉴定的基因(TAC1)定位相同,但利用一个BC2F2群体将qTAC8定位到标记RM7049和RM23175之间的一个16.5 cM区域。通过两个遗传分离群体将qTAC8的位置缩小到一个92 kb的DNA区域。最后,根据基因组测序和qRT-PCR分析,将一个开放阅读框(ORF)视为候选基因。此外,创建了一组四个近等基因系(NIL)来研究这两个QTL之间的遗传关系,一个携带qTAC8和qTAC9的株系表现出分蘖角度的加性效应,表明这些QTL参与了不同的遗传途径。我们的结果为qTAC8的克隆和水稻株型的遗传改良提供了基础。