State Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Sciences, Fudan University , Shanghai 200433, China.
Breed Sci. 2012 Dec;62(4):310-9. doi: 10.1270/jsbbs.62.310. Epub 2012 Dec 1.
Heading date in rice (Oryza sativa L.) is a critical agronomic trait with a complex inheritance. To investigate the genetic basis and mechanism of gene interaction in heading date, we conducted genetic analysis on segregation populations derived from crosses among the indica cultivars Bo B, Yuefeng B and Baoxuan 2. A set of dominant complementary genes controlling late heading, designated LH1 and LH2, were detected by molecular marker mapping. Genetic analysis revealed that Baoxuan 2 contains both dominant genes, while Bo B and Yuefeng B each possess either LH1 or LH2. Using larger populations with segregant ratios of 3 : 1, we fine-mapped LH1 to a 63-kb region near the centromere of chromosome 7 flanked by markers RM5436 and RM8034, and LH2 to a 177-kb region on the short arm of chromosome 8 between flanking markers Indel22468-3 and RM25. Some candidate genes were identified through sequencing of Bo B and Yuefeng B in these target regions. Our work provides a solid foundation for further study on gene interaction in heading date and has application in marker-assisted breeding of photosensitive hybrid rice in China.
水稻抽穗期是一个重要的农艺性状,具有复杂的遗传基础。为了研究抽穗期的基因互作遗传基础和机制,我们利用籼稻品种博白 B、越丰 B 和宝轩 2 构建的分离群体进行了遗传分析。通过分子标记定位,检测到一组控制晚抽穗的显性互补基因,命名为 LH1 和 LH2。遗传分析表明,宝轩 2 同时含有这两个显性基因,而博白 B 和越丰 B 各含有 LH1 或 LH2 中的一个。利用具有 3:1 分离比的较大群体,我们将 LH1 精细定位到第 7 号染色体着丝粒附近的 63-kb 区域,位于标记 RM5436 和 RM8034 之间,将 LH2 定位到第 8 号染色体短臂上的 177-kb 区域,位于标记 Indel22468-3 和 RM25 之间。通过对这些目标区域中的博白 B 和越丰 B 进行测序,鉴定了一些候选基因。我们的工作为进一步研究抽穗期的基因互作提供了坚实的基础,并为中国感光型杂交水稻的分子标记辅助育种提供了应用价值。