Agarwal Surekha, Tripura Venkata V G N, Kotla Anuradha, Mangrauthia Satendra Kumar, Neelamraju Sarla
Directorate of Rice Research, Hyderabad 500030, India.
Gene. 2014 Aug 10;546(2):430-6. doi: 10.1016/j.gene.2014.05.069. Epub 2014 Jun 2.
Identifying QTLs/genes for iron and zinc in rice grains can help in biofortification programs. Genome wide mapping showed 14 QTLs for iron and zinc concentration in unpolished rice grains of F7 RILs derived from Madhukar × Swarna. One line (HL) with high Fe and Zn and one line (LL) with low Fe and Zn in unpolished rice were compared with each other for gene expression using qPCR. 7 day old seedlings were grown in Fe+ and Fe- medium for 10 days and RNA extracted from roots and shoots to determine the response of 15 genes in Fe- conditions.
HL showed higher upregulation than LL in shoots but LL showed higher upregulation than HL in roots. YSL2 was upregulated only in HL roots and YSL15 only in HL shoots and both up to 60 fold under Fe- condition. IRT2 and DMAS1 were upregulated 100 fold and NAS2 1000 fold in HL shoot. NAS2, IRT1, IRT2 and DMAS1 were upregulated 40 to 100 fold in LL roots. OsZIP8, OsNAS3, OsYSL1 and OsNRAMP1 which underlie major Fe QTL showed clear allelic differences between HL and LL for markers flanking QTL. The presence of iron increasing QTL allele in HL was clearly correlated with high expression of the underlying gene. OsZIP8 and OsNAS3 which were within major QTL with increasing effect from Madhukar were 8 fold and 4 fold more expressed in HL shoot than in LL shoot. OsNAS1, OsNAS2, OsNAS3, OsYSL2 and OsYSL15 showed 1.5 to 2.5 fold upregulation in flag leaf of HL when compared with flag leaf of Swarna.
HL and LL differed in root length, Fe concentration and expression of several genes under Fe deficiency. The major distinguishing genes were NAS2, IRT2, DMAS1, and YSL15 in shoot and NAS2, IRT1, IRT2, YSL2, and ZIP8 in roots. The presence of iron increasing QTL allele in HL at marker locus close to genes also increased upregulation in HL.
鉴定水稻籽粒中铁和锌的数量性状基因座(QTLs)/基因有助于生物强化计划。全基因组图谱显示,在源自Madhukar×Swarna的F7重组自交系(RILs)的糙米籽粒中,有14个铁和锌浓度的QTL。使用定量聚合酶链反应(qPCR)比较了糙米中一个高铁和锌含量的品系(HL)和一个低铁和锌含量的品系(LL)之间的基因表达。将7日龄的幼苗在铁充足(Fe+)和铁缺乏(Fe-)的培养基中培养10天,然后从根和芽中提取RNA,以确定15个基因在铁缺乏条件下的反应。
在芽中,HL的上调程度高于LL,但在根中,LL的上调程度高于HL。黄色条纹蛋白2(YSL2)仅在HL根中上调,黄色条纹蛋白15(YSL15)仅在HL芽中上调,并且在铁缺乏条件下两者均上调至60倍。在HL芽中,铁调节转运蛋白2(IRT2)和脱氧麦根酸合酶1(DMAS1)上调100倍,烟酰胺合酶2(NAS2)上调1000倍。在LL根中,NAS2、IRT1、IRT2和DMAS1上调40至100倍。位于主要铁QTL的锌转运蛋白8(OsZIP8)、烟酰胺合酶3(OsNAS3)、黄色条纹蛋白1(OsYSL1)和天然抗性相关巨噬蛋白1(OsNRAMP1)在HL和LL之间,对于QTL侧翼标记显示出明显的等位基因差异。HL中铁增加QTL等位基因的存在与潜在基因的高表达明显相关。来自Madhukar且具有增加效应的主要QTL内的OsZIP8和OsNAS3在HL芽中的表达比在LL芽中高8倍和4倍。与Swarna的旗叶相比,HL旗叶中的NAS1,、NAS2、NAS3、YSL2和YSL15上调了1.5至2.5倍。
HL和LL在缺铁条件下的根长、铁浓度和几个基因的表达方面存在差异。主要的区别基因在芽中是NAS2、IRT2、DMAS1和YSL15,在根中是NAS2、IRT1、IRT2、YSL2和ZIP8。HL中靠近基因的标记位点处铁增加QTL等位基因的存在也增加了HL中的上调。