Krishnamurthy S L, Sharma P C, Dewan D, Lokeshkumar B M, Rathor Suman, Warraich A S, Vinaykumar N M, Leung Hei, Singh R K
Central Soil Salinity Research Institute, Karnal, India.
Kuvempu University, Shankaraghatta, Shimvamogga India.
Physiol Mol Biol Plants. 2022 Apr;28(4):819-835. doi: 10.1007/s12298-022-01174-8. Epub 2022 Apr 21.
The present study was conducted to identify the novel QTLs controlling salinity and sodicity tolerance using MAGIC rice population. Phenotyping was carried out in salinity (EC ~ 10 dS/m) and sodicity (pH ~ 9.8) at the seedling stage. Among 391 lines, 43 and 98 lines were found tolerant and moderately tolerant to salinity. For sodicity condition, 2 and 45 lines were showed tolerance and moderately tolerance at seedling stage. MAGIC population was genotyped with the help of genotyping by sequencing (GBS) and filtered 27041SNPs were used for genome wide marker trait association studies. With respect to salinity tolerance, 25 SNPs were distributed on chromosomes 1, 5, 11 and 12, whereas 18 SNPs were mapped on chromosomes 6, 4 and 11 with LOD value of > 3.25 to sodicity tolerance in rice. The candidate gene analysis detected twelve causal genes including gene at region for salinity and six associated genes for sodic stress tolerance. The significant haplotypes responsible for core histone protein coding gene () and three uncharacterized protein coding genes (, and ) were identified under saline stress. Likewise, five significant haplotypes coding for ribose 5-phosphate isomerise (), aspartyl protease (), aluminum-activated malate transporter (), OsFBX421-Fbox domain containing protein () and one uncharacterized protein () were detected for sodic stress tolerance. The identified novel SNPs could be the potential candidates for functional characterization. These candidate genes aid to further understanding of genetic mechanism on salinity and sodicity stress tolerance in rice. The tolerant line could be used in future breeding programme to enhance the salinity and sodicity tolerance in rice.
The online version contains supplementary material available at 10.1007/s12298-022-01174-8.
本研究旨在利用多亲本高级世代互交群体(MAGIC)水稻群体鉴定控制耐盐性和耐苏打性的新数量性状位点(QTL)。在幼苗期对盐度(电导率10 dS/m)和苏打度(pH9.8)条件下进行表型分析。在391个株系中,发现43个和98个株系对盐度具有耐受性和中度耐受性。对于苏打度条件,在幼苗期有2个和45个株系表现出耐受性和中度耐受性。借助测序基因分型(GBS)对MAGIC群体进行基因分型,并使用经过筛选的27041个单核苷酸多态性(SNP)进行全基因组标记-性状关联研究。关于耐盐性,25个SNP分布在第1、5、11和12号染色体上,而18个SNP定位在第6、4和11号染色体上,与水稻耐苏打性的对数似然比(LOD)值>3.25。候选基因分析检测到12个因果基因,包括一个与盐度相关区域的基因和6个与耐苏打胁迫相关的基因。在盐胁迫下,鉴定出负责核心组蛋白编码基因()以及三个未表征蛋白编码基因(、和)的显著单倍型。同样,检测到五个编码磷酸核糖异构酶()、天冬氨酰蛋白酶()、铝激活苹果酸转运蛋白()、含OsFBX421-Fbox结构域蛋白()和一个未表征蛋白()的显著单倍型,用于耐苏打胁迫。鉴定出的新SNP可能是功能表征的潜在候选者。这些候选基因有助于进一步了解水稻耐盐性和耐苏打性胁迫的遗传机制。耐盐株系可用于未来的育种计划,以提高水稻的耐盐性和耐苏打性。
在线版本包含可在10.1007/s12298-022-01174-8获取的补充材料。