Liu Hongjun, Shi Junpeng, Sun Chuanlong, Gong Hao, Fan Xingming, Qiu Fazhan, Huang Xuehui, Feng Qi, Zheng Xixi, Yuan Ningning, Li Changsheng, Zhang Zhiyong, Deng Yiting, Wang Jiechen, Pan Guangtang, Han Bin, Lai Jinsheng, Wu Yongrui
National Key Laboratory of Plant Molecular Genetics, Chinese Academy of Sciences Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology & Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China;
State Key Laboratory of Agrobiotechnology and National Maize Improvement Center, Department of Plant Genetics and Breeding, China Agricultural University, Beijing 100193, China;
Proc Natl Acad Sci U S A. 2016 May 3;113(18):4964-9. doi: 10.1073/pnas.1601352113. Epub 2016 Apr 18.
The maize opaque2 (o2) mutant has a high nutritional value but it develops a chalky endosperm that limits its practical use. Genetic selection for o2 modifiers can convert the normally chalky endosperm of the mutant into a hard, vitreous phenotype, yielding what is known as quality protein maize (QPM). Previous studies have shown that enhanced expression of 27-kDa γ-zein in QPM is essential for endosperm modification. Taking advantage of genome-wide association study analysis of a natural population, linkage mapping analysis of a recombinant inbred line population, and map-based cloning, we identified a quantitative trait locus (qγ27) affecting expression of 27-kDa γ-zein. qγ27 was mapped to the same region as the major o2 modifier (o2 modifier1) on chromosome 7 near the 27-kDa γ-zein locus. qγ27 resulted from a 15.26-kb duplication at the 27-kDa γ-zein locus, which increases the level of gene expression. This duplication occurred before maize domestication; however, the gene structure of qγ27 appears to be unstable and the DNA rearrangement frequently occurs at this locus. Because enhanced expression of 27-kDa γ-zein is critical for endosperm modification in QPM, qγ27 is expected to be under artificial selection. This discovery provides a useful molecular marker that can be used to accelerate QPM breeding.
玉米 opaque2(o2)突变体具有较高的营养价值,但它会发育出粉质胚乳,这限制了其实际应用。对 o2 修饰基因进行遗传选择可以将突变体正常的粉质胚乳转化为坚硬的玻璃质表型,从而产生所谓的优质蛋白玉米(QPM)。先前的研究表明,QPM 中 27-kDa γ-醇溶蛋白的表达增强对于胚乳修饰至关重要。利用自然群体的全基因组关联研究分析、重组自交系群体的连锁图谱分析以及图位克隆技术,我们鉴定出了一个影响 27-kDa γ-醇溶蛋白表达的数量性状位点(qγ27)。qγ27 被定位到与 7 号染色体上主要的 o2 修饰基因(o2 modifier1)相同的区域,靠近 27-kDa γ-醇溶蛋白基因座。qγ27 是由 27-kDa γ-醇溶蛋白基因座处的一个 15.26-kb 重复产生的,这增加了基因表达水平。这种重复发生在玉米驯化之前;然而,qγ27 的基因结构似乎不稳定,DNA 重排在该基因座频繁发生。由于 27-kDa γ-醇溶蛋白的表达增强对于 QPM 的胚乳修饰至关重要,qγ27 有望受到人工选择。这一发现提供了一个有用的分子标记,可用于加速 QPM 育种。