Xu Yanhao, Jia Qiaojun, Zhou Gaofeng, Zhang Xiao-Qi, Angessa Tefera, Broughton Sue, Yan George, Zhang Wenying, Li Chengdao
Hubei Collaborative Innovation Center for Grain Industry/College of Agriculture, Yangtze University, Jingzhou, Hubei, 434000, China.
Western Barley Genetics Alliance, Murdoch University, Murdoch, WA6150, Australia.
BMC Plant Biol. 2017 Jan 13;17(1):11. doi: 10.1186/s12870-016-0964-4.
The dwarfing gene sdw1 has been widely used throughout the world to develop commercial barley varieties. There are at least four different alleles at the sdw1 locus.
Mutations in the gibberellin 20-oxidase gene (HvGA20ox2) resulted in multiple alleles at the sdw1 locus. The sdw1.d allele from Diamant is due to a 7-bp deletion in exon 1, while the sdw1.c allele from Abed Denso has 1-bp deletion and a 4-bp insertion in the 5' untranslated region. The sdw1.a allele from Jotun resulted from a total deletion of the HvGA20ox2 gene. The structural changes result in lower gene expression in sdw1.d and lack of expression in sdw1.a. There are three HvGA20ox genes in the barley genome. The partial or total loss of function of the HvGA20ox2 gene could be compensated by enhanced expression of its homolog HvGA20ox1and HvGA20ox3. A diagnostic molecular marker was developed to differentiate between the wild-type, sdw1.d and sdw1.a alleles and another molecular marker for differentiation of sdw1.c and sdw1.a. The markers were further tested in 197 barley varieties, out of which 28 had the sdw1.d allele and two varieties the sdw1.a allele. To date, the sdw1.d and sdw1.a alleles have only been detected in the modern barley varieties and lines.
The results provided further proof that the gibberellin 20-oxidase gene (HvGA20ox2) is the functional gene of the barley sdw1 mutants. Different deletions resulted in different functional alleles for different breeding purposes. Truncated protein could maintain partial function. Partial or total loss of function of the HvGA20ox2 gene could be compensated by enhanced expression of its homolog HvGA20ox1 and HvGA20ox3.
矮化基因sdw1已在全球广泛用于培育商业大麦品种。sdw1位点至少有四个不同的等位基因。
赤霉素20-氧化酶基因(HvGA20ox2)中的突变导致了sdw1位点的多个等位基因。来自 Diamant 的sdw1.d等位基因是由于外显子1中7个碱基对的缺失,而来自Abed Denso的sdw1.c等位基因在5'非翻译区有1个碱基对的缺失和4个碱基对的插入。来自Jotun的sdw1.a等位基因是由于HvGA20ox2基因的完全缺失。这些结构变化导致sdw1.d中基因表达降低,而sdw1.a中缺乏表达。大麦基因组中有三个HvGA20ox基因。HvGA20ox2基因部分或全部功能丧失可通过其同源基因HvGA20ox1和HvGA20ox3的表达增强来补偿。开发了一种诊断分子标记来区分野生型、sdw1.d和sdw1.a等位基因,以及另一种用于区分sdw1.c和sdw1.a的分子标记。这些标记在197个大麦品种中进一步测试,其中28个具有sdw1.d等位基因,两个品种具有sdw1.a等位基因。迄今为止,sdw1.d和sdw1.a等位基因仅在现代大麦品种和品系中被检测到。
结果进一步证明赤霉素20-氧化酶基因(HvGA20ox2)是大麦sdw1突变体的功能基因。不同的缺失导致了用于不同育种目的的不同功能等位基因。截短的蛋白质可以维持部分功能。HvGA20ox2基因部分或全部功能丧失可通过其同源基因HvGA20ox1和HvGA20ox3的表达增强来补偿。